69 results on '"Cordisco M"'
Search Results
2. 263 Development of secondary neoplasms in patients with nevus sebaceous
- Author
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Burli, A., primary, Bawany, F., additional, and Cordisco, M., additional
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- 2022
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3. Sopra- o sovra-? E dopo si raddoppia?
- Author
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Cordisco, M. and Iacobini, C.
- Subjects
formazione delle parole ,formazione delle parole, italiano e influsso dell'inglese ,italiano e influsso dell'inglese - Abstract
Le parole prefissate con sopra- / sovra- suscitano in molti lettori dubbi sulla preferenza da accordare all’una o all’altra forma del prefisso e al loro impiego con o senza raddoppiamento in parole quali: sopralluogo / sovralluogo, soprastante / sovrastante, sopracitato / sopraccitato / sovracitato / sovraccitato, soprannumerario / sovrannumerario, soprascrivere / sovrascrivere; altre domande riguardano l’esistenza o l’ammissibilità di alcune parole, tra cui soprastimare, sovralzo.
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- 2022
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4. Rapidly involuting congenital haemangioma associated with transient thrombocytopenia and coagulopathy: a case series
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Baselga, E., Cordisco, M. R., Garzon, M., Lee, M. T., Alomar, A., and Blei, F.
- Published
- 2008
5. Four common glomulin mutations cause two thirds of glomuvenous malformations (“familial glomangiomas”): evidence for a founder effect
- Author
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Brouillard, P, Ghassibé, M, Penington, A, Boon, L M, Dompmartin, A, Temple, I K, Cordisco, M, Adams, D, Piette, F, Harper, J I, Syed, S, Boralevi, F, Taïeb, A, Danda, S, Baselga, E, Enjolras, O, Mulliken, J B, and Vikkula, M
- Published
- 2005
6. Text analysis and authentic material in the ESP classroom.
- Author
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Anderson, R, Banelli, D, Cordisco, M, Di Sabato, B, Filippone, A, Papini, L, Hotimsky, F, Orsini Jones, M, Jones, D, Pratesi, D, Iodice, M, ANDERSON, ROBIN, Banelli, D., Cordisco, M., Di Sabato, B., Filippone, A., Papini, L., Hotimsky, F., Orsini Jones, M., Jones, D., Pratesi, D., Iodice, M., Anderson, R, Banelli, D, Cordisco, M, Di Sabato, B, Filippone, A, Papini, L, Hotimsky, F, Orsini Jones, M, Jones, D, Pratesi, D, Iodice, M, ANDERSON, ROBIN, Banelli, D., Cordisco, M., Di Sabato, B., Filippone, A., Papini, L., Hotimsky, F., Orsini Jones, M., Jones, D., Pratesi, D., and Iodice, M.
- Abstract
"Che cosa rende un testo difficile? Quali conoscenze e abilità sono necessarie per decodificare un testo ? In che modo il testo si articola per trasmettere il messaggio dell'autore? In che rapporto stanno le scelte linguistiche e i molti contesti speciftci in cui la lingua viene naturalmen-te a trovarsi, e quali i tratti macro e micro linguistici utilizzati dagli autori per veicolare le loro idee? Il seguente contributo intende discutere come in Facoltà universitarie che non siano di Lingue, laddove si tengono corsi di lingua straniera, nel nostro caso di inglese, per scopi specifici e accademici, l'impiego di materiali autentici sia essenziale, ma richieda da parte del docente di lingua l'impegno a sensibilizzare gli sludenti alla elevata incidenza di riferimenti esterni al testo a loro proposto e alla varietà di espressione per trasmettere le informazioni che l'autore fornisce unitamente anche al suo messaggio e al suo punto di vista. Attraverso un appropriata analisi del discorso si mira a rendere gli studenti maggiormente consapevoli delle caratteristiche di stile e di registro che i vari autori riversano nei loro testi in modo da agevolarne e renderne più efficace la codificazione.
- Published
- 2002
7. Blue Rubber Bleb Nevus (BRBN) Syndrome Is Caused by Somatic TEK (TIE2) Mutations.
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Soblet, J., Kangas, J., Nätynki, M., Mendola, A., Helaers, R., Uebelhoer, M., Kaakinen, M., Cordisco, M., Dompmartin, A., Enjolras, O., Holden, S., Irvine, A.D., Kangesu, L., Léauté-Labrèze, C., Lanoel, L., Lokmic, Z., Maas, S., McAleer, M.A., Penington, A., Rieu, P.N.M.A., Syed, S., Vleuten, C.J.M. van der, Watson, R., Fishman, S.J., Mulliken, J.B., Eklund, L., Limaye, N., Boon, L.M., Vikkula, M., Soblet, J., Kangas, J., Nätynki, M., Mendola, A., Helaers, R., Uebelhoer, M., Kaakinen, M., Cordisco, M., Dompmartin, A., Enjolras, O., Holden, S., Irvine, A.D., Kangesu, L., Léauté-Labrèze, C., Lanoel, L., Lokmic, Z., Maas, S., McAleer, M.A., Penington, A., Rieu, P.N.M.A., Syed, S., Vleuten, C.J.M. van der, Watson, R., Fishman, S.J., Mulliken, J.B., Eklund, L., Limaye, N., Boon, L.M., and Vikkula, M.
- Abstract
Item does not contain fulltext
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- 2016
8. Text analysis and authentic material in the ESP classroom
- Author
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ANDERSON, ROBIN, Banelli, D., Cordisco, M., Di Sabato, B., Filippone, A., Papini, L., Hotimsky, F., Orsini Jones, M., Jones, D., Pratesi, D., Iodice, M., Anderson, R, Banelli, D, Cordisco, M, Di Sabato, B, Filippone, A, Papini, L, Hotimsky, F, Orsini Jones, M, Jones, D, Pratesi, D, and Iodice, M
- Subjects
L-LIN/12 - LINGUA E TRADUZIONE - LINGUA INGLESE ,text analysis, authentic material, ESP, classroom - Abstract
"Che cosa rende un testo difficile? Quali conoscenze e abilità sono necessarie per decodificare un testo ? In che modo il testo si articola per trasmettere il messaggio dell'autore? In che rapporto stanno le scelte linguistiche e i molti contesti speciftci in cui la lingua viene naturalmen-te a trovarsi, e quali i tratti macro e micro linguistici utilizzati dagli autori per veicolare le loro idee? Il seguente contributo intende discutere come in Facoltà universitarie che non siano di Lingue, laddove si tengono corsi di lingua straniera, nel nostro caso di inglese, per scopi specifici e accademici, l'impiego di materiali autentici sia essenziale, ma richieda da parte del docente di lingua l'impegno a sensibilizzare gli sludenti alla elevata incidenza di riferimenti esterni al testo a loro proposto e alla varietà di espressione per trasmettere le informazioni che l'autore fornisce unitamente anche al suo messaggio e al suo punto di vista. Attraverso un appropriata analisi del discorso si mira a rendere gli studenti maggiormente consapevoli delle caratteristiche di stile e di registro che i vari autori riversano nei loro testi in modo da agevolarne e renderne più efficace la codificazione.
- Published
- 2002
9. Agminated, Eruptive Pyogenic Granuloma-Like Lesions Developing over Congenital Vascular Stains
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Baselga, E, Wassef, M, Lopez, S, Hoffman, W, Cordisco, M, and Frieden, IJ
- Abstract
We report three infants who developed agminated pyogenic granulomas over congenital vascular malformations, all of which had an aggressive growth pattern. There were no precipitating events such as laser therapy or surgery. Lesions were excised.
- Published
- 2012
10. A Novel Association between RASA1 Mutations and Spinal Arteriovenous Anomalies.
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UCL - Cliniques universitaires Saint-Luc, UCL - MD/CHIR - Département de chirurgie, UCL - MD/BICL - Département de biochimie et de biologie cellulaire, Thiex, R, Revencu, Nicole, Boon, Laurence M., Mulliken, J B, Burrows, P E, Cordisco, M, Dwight, Y, Smith, E R, Vikkula, Miikka, Orbach, D B, UCL - Cliniques universitaires Saint-Luc, UCL - MD/CHIR - Département de chirurgie, UCL - MD/BICL - Département de biochimie et de biologie cellulaire, Thiex, R, Revencu, Nicole, Boon, Laurence M., Mulliken, J B, Burrows, P E, Cordisco, M, Dwight, Y, Smith, E R, Vikkula, Miikka, and Orbach, D B
- Abstract
BACKGROUND AND PURPOSE: CM-AVM is a recently recognized autosomal dominant disorder associated with mutations in RASA1. Arteriovenous lesions have been reported in the brain, limbs, and the face in 18.5% of patients. We report a novel association between RASA1 mutations and spinal arteriovenous anomalies. MATERIALS AND METHODS: In a collaborative study, 5 index patients (2 females, 3 males) with spinal AVMs or AVFs and cutaneous multifocal capillary lesions were investigated for the RASA1 gene mutation. RESULTS: All 5 patients were found to have RASA1 mutation (2 de novo, 3 familial), and all had multifocal capillary malformations at birth. Neurologic deficits developed at ages ranging from infancy to early adulthood. All spinal anomalies (2 AVMs at the conus, 1 AVM at the lumbosacral junction, and 1 cervical and 1 cervicothoracic AVF) were complex, extensive, and fast-flow lesions. All patients required treatment based on the clinical and/or radiologic appearance of the lesions. CONCLUSIONS: To our knowledge, an association of RASA1 mutation and spinal AVM/AVF has not been described. MR imaging screening of patients with characteristic CMs and neurologic symptoms presenting at a young age may be useful in detecting the presence of fast-flow intracranial or intraspinal arteriovenous anomalies before potentially significant neurologic insult has occurred.
- Published
- 2009
11. Four common glomulin mutations cause two thirds of glomuvenous malformations ('familial glomangiomas'): evidence for a founder effect.
- Author
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UCL - MD/BICL - Département de biochimie et de biologie cellulaire, UCL - MD/CHIR - Département de chirurgie, Brouillard, Pascal, Ghassibé, Michella, Penington, A, Boon, Laurence M., Dompmartin, Anne, Temple, I K, Cordisco, M, Adams, D., Piette, F, Harper, J I, Syed, S, Boralevi, F, Taïeb, A, Danda, S, Baselga, E, Enjolras, O, Mulliken, J B, Vikkula, Miikka, UCL - MD/BICL - Département de biochimie et de biologie cellulaire, UCL - MD/CHIR - Département de chirurgie, Brouillard, Pascal, Ghassibé, Michella, Penington, A, Boon, Laurence M., Dompmartin, Anne, Temple, I K, Cordisco, M, Adams, D., Piette, F, Harper, J I, Syed, S, Boralevi, F, Taïeb, A, Danda, S, Baselga, E, Enjolras, O, Mulliken, J B, and Vikkula, Miikka
- Abstract
BACKGROUND: Glomuvenous malformation (GVM) ("familial glomangioma") is a localised cutaneous vascular lesion histologically characterised by abnormal smooth muscle-like "glomus cells" in the walls of distended endothelium lined channels. Inheritable GVM has been linked to chromosome 1p21-22 and is caused by truncating mutations in glomulin. A double hit mutation was identified in one lesion. This finding suggests that GVM results from complete localised loss of function and explains the paradominant mode of inheritance. OBJECTIVE: To report on the identification of a mutation in glomulin in 23 additional families with GVM. RESULTS: Three mutations are new; the others have been described previously. Among the 17 different inherited mutations in glomulin known up to now in 43 families, the 157delAAGAA mutation is the most common and was present in 21 families (48.8%). Mutation 108C-->A was found in five families (11.8%), and the mutations 554delA+556delCCT and 1179delCAA were present together in two families (4.7% each). Polymorphic markers suggested a founder effect for all four mutations. CONCLUSIONS: Screening for these mutations should lead to a genetic diagnosis in about 70% of patients with inherited GVM. So far, a mutation in glomulin has been found in all GVM families tested, thus demonstrating locus homogeneity.
- Published
- 2005
12. A Novel Association betweenRASA1Mutations and Spinal Arteriovenous Anomalies
- Author
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Thiex, R., primary, Mulliken, J.B., additional, Revencu, N., additional, Boon, L.M., additional, Burrows, P.E., additional, Cordisco, M., additional, Dwight, Y., additional, Smith, E.R., additional, Vikkula, M., additional, and Orbach, D.B., additional
- Published
- 2009
- Full Text
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13. Infantile Hemangiomas in Twins: A Prospective Cohort Study.
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Greco, M. Fernanda, Frieden, Ilona J., Drolet, Beth A., Garzon, María C., Mancini, Anthony J., Chamlin, Sarah L., Metry, Denise, Adams, Denise, Lucky, Anne, Wentzel, Mary Sue, Horii, Kimberly A., Baselga, Eulalia, McCuaig, Catherine C., Powell, Julie, Haggstrom, Anita, Siegel, Dawn, Morel, Kimberly D., Cordisco, M. Rosa, Nopper, Amy J., and Krol, Alfons
- Subjects
HEMANGIOMAS ,DISEASES in twins ,INFANT diseases ,PEDIATRIC dermatology ,SKIN diseases - Abstract
Background Twins have a higher-than-expected risk of infantile hemangiomas (IHs), but the exact reasons for this association are not clear. Comparing concordant and discordant twin pairs might help elucidate these factors and yield more information about IH risk factors. Methods A prospective cohort study of twin pairs from 12 pediatric dermatology centers in the United States, Canada, Argentina, and Spain was conducted. Information regarding maternal pregnancy history, family history of vascular birthmarks, zygosity (if known), and pregnancy-related information was collected. Information regarding twins ( N = 202 sets) included birthweight, gestational age (GA), presence or absence of IHs, numbers and subtypes of IHs, presence of other birthmarks, and other medical morbidities. Results Two hundred two sets of twins were enrolled. Concordance for IH was present in 37% of twin pairs. Concordance for IH was inversely related to gestational age (GA), present in 42% of GA of 32 weeks or less, 36% of GA of 33 to 36 weeks, and 32% of GA of 37 weeks or more. Twins of GA of 34 weeks or less were more than two and a half times as likely to be concordant as those of GA of 35 weeks or more (odds ratio (OR) = 2.66, 95% confidence interval (CI) = 1.42-4.99; p < 0.01). In discordant twins, lower birthweight conferred a high risk of IH; of the 64 sets of twins with 10% or greater difference in weight, the smaller twin had IH in 62.5% ( n = 40) of cases, versus 37.5% ( n = 24) of cases in which the higher-birthweight twin was affected. Zygosity was reported in 188 twin sets (93%). Of these, 78% were dizygotic and 22% monozygotic. There was no statistically significant difference in rates of concordance between monozygotic twins (43%, 18/42) and dizygotic twins (36%, 52/146) (p = 0.50). In multivariate analysis comparing monozygotic and dizygotic twins, adjusting for effects of birthweight and sex, the likelihood of concordance for monozygotic was not appreciably higher than that for dizygotic twins (OR = 1.14, 95% CI = 0.52-2.49). Female sex also influenced concordance, confirming the effects of female sex on IH risk. The female-to-male ratio was 1.7:1 in the entire cohort and 1.9:1 in those with IH. Of the 61 concordant twin sets with known sex of both twins, 41% were female/female, 43% were female/male, and 16% were male/male. Conclusions These findings suggest that the origin of IHs is multifactorial and that predisposing factors such as birthweight, sex, and GA may interact with one another such that a threshold is reached for clinical expression. [ABSTRACT FROM AUTHOR]
- Published
- 2016
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14. Low Incidence of Myocardial Recovery After Left Ventricular Assist Device Implantation in Patients with Chronic Heart Failure.
- Author
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Mancini, D M, primary, Beniaminovitz, A, additional, Levin, H, additional, Catanese, K, additional, Flannery, M, additional, DiTullio, M, additional, Savin, S, additional, Cordisco, M E, additional, Rose, E, additional, and Oz, M., additional
- Published
- 1999
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15. Culture, identity and territory: Reflections for the development of a strategy of service differentiation in agritourism ventures of a Group of Rural Change (INTA) in Coronel Suárez (Buenos Aires),Cultura, identidad Y territorio: reflexiones para el desarrollo de una estrategia de diferenciación del servicio agroturístico en emprendimientos de un Grupo de Cambio Rural (INTA) del partido de Coronel Suárez (Buenos Aires)
- Author
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Cordisco, M., Scoponi, L., Batista, M., Regina Durán, Bustos Cara, R., Haag, M. I., and Piñeiro, V.
16. Possible PHACES syndrome: Segmental thoracobrachial hemangioma associated with extracutaneous manifestations
- Author
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Manunza, F., CATERINA FERRELI, Cordisco, M. R., and Pau, M.
17. Possible PHACES syndrome: segmental thoracobrachial hemangioma associated with extracutaneous manifestations.
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Manunza, F., Ferreli, C., Cordisco, M. R., and Pau, M.
- Subjects
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BLOOD-vessel tumors , *CONGENITAL heart disease , *HEART abnormalities - Abstract
In PHACES syndrome a facial infantile hemangiomas (IH) is associated with extracutaneous manifestations involving the central nervous system, heart, blood vessels of head and neck, eye and sternum. Recently, an IH of the upper trunk was reported in association with extravcutaneous manifestations reminiscent of PHACES syndrome. Here we report a case of a 7-month-old girl with segmental hemangioma involving the upper trunk and limb. It was associated with structural anomalies similar to those reported in PHACES syndrome, including congenital heart disease, arterial abnormalities and a sternal defect; moreover there was a late-onset small hemangioma of the face. [ABSTRACT FROM AUTHOR]
- Published
- 2014
18. Rabdomiosarcoma a localizzazione cutanea.
- Author
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Lanoël, A., Fain, A., Cervini, B., Merediz, J., Bocian, M., García Díaz, R., Cordisco, M. R., González, M. T., Laterza, A., Gallo, G., Dávila, M. T., and Pierini, A.M.
- Abstract
Il rabdomiosarcoma è il più frequente tumore delle parti molli nei primi 15 anni di vita, ma i casi con interessamento della cute sono estremamente rari. Materiale e metodi. Si tratta di un'analisi retrospettiva di tutti i pazienti con rabdomiosarcoma cutaneo, volta ad appurare il loro decorso clinico e la risposta al trattamento. Risultati. Tra agosto 1988 e gennaio 2005 abbiamo individuato 353 casi di rabdomiosarcoma, 15 dei quali (4,2%) esibivano un interessamento cutaneo al momento della diagnosi. La sede primitiva cutanea più frequente era il volto -9 pazienti-. Per quanto riguarda il decorso clinico, 6/15 pazienti sono stati persi di vista. Dei restanti 9 pazienti 5 sono deceduti, 3 sono liberi da malattia e uno è ancora in trattamento ma senza recidive. Conclusioni. A nostro parere bisogna prendere in considerazione questa diagnosi in caso di tumori a crescita molto rapida e differenziarla da altri tumori infantili. [ABSTRACT FROM AUTHOR]
- Published
- 2009
19. Use of telemonitoring to decrease the rate of hospitalization in patients with severe congestive heart failure.
- Author
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Codisco ME, Beniaminovitz A, Hammond K, Mancini D, Cordisco, M E, Benjaminovitz, A, Hammond, K, and Mancini, D
- Abstract
We investigated whether the application of a home-based telemonitoring system could decrease hospital admissions and emergency room visits in 30 patients with severe congestive heart failure compared with 51 patients with congestive heart failure who received standard therapy. Emergency room visits (1 vs 11) and hospitalizations (13 vs 36) were decreased in the telemonitored group (both p <0.05). [ABSTRACT FROM AUTHOR]
- Published
- 1999
20. Transport-related respiratory pathogens in horses travelling long distances: A prospective study on arrival at the slaughterhouse.
- Author
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Padalino B, Pellegrini F, Felici M, Zappaterra M, Catella C, Cordisco M, Lorusso E, Cirone F, and Pratelli A
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- Animals, Horses, Prospective Studies, Transportation, Italy epidemiology, Male, Female, Prevalence, Respiratory Tract Infections veterinary, Respiratory Tract Infections virology, Respiratory Tract Infections microbiology, Respiratory Tract Infections epidemiology, Pasteurellaceae isolation & purification, Horse Diseases microbiology, Horse Diseases epidemiology, Horse Diseases virology, Abattoirs
- Abstract
Respiratory disorders (RDs) are a common transport-related welfare consequence in horses. This prospective study described the journeys of horses transported to two slaughterhouses in Italy, documented the prevalence of potentially RD-related pathogens, and identified possible predisposing factors. Data were recorded from arrival until 48 h after arrival and included the collection of Deep Nasopharyngeal Swabs (DNS), journey details and welfare assessment of horses (n = 155). PCR was used to quantify the presence of influenza A virus, reovirus, equine herpesvirus type 1 and 4, adenovirus, rhinovirus, astrovirus, equine coronavirus, Pasteurellaceae, Streptococcus equi sub. equi and sub. zooepidemicus. One horse each tested positive for reovirus, and rhinovirus and two horses tested positive for adenovirus. The prevalence of Streptococcus equi and zooepidemicus and Pasteurellaceae was 4 %, 19 % and 63 % respectively. Streptococcaceae and Pasteurellaceae were associated with sweating (P < 0.001). In addition, Streptococcaceae was associated with abnormal demeanour (P = 0.003), nasal or ocular discharge (P < 0.001) and higher compromised welfare after transport (P < 0.001). The multivariable regression analysis showed that broken horses departing from Eastern Europe or France were more likely to test positive for Streptococcaceae than unbroken horses coming from Poland (model P < 0.001), while broken horses subjected to short stops en route were more likely to test positive for Pasteurellaceae than unbroken horses on journeys without stops (model P < 0.001). Our findings increase the understanding of predisposing factors for RDs and may be useful in the implementation of regulations to protect the welfare of horse during transport., Competing Interests: Declaration of competing interest The authors declare no conflict of interest., (Copyright © 2024 The Author(s). Published by Elsevier Ltd.. All rights reserved.)
- Published
- 2025
- Full Text
- View/download PDF
21. Occurrence of bacteremia, bacteriuria and bacteriuria-related bacteremia in dogs and cats with chronic kidney disease. A pilot study.
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Uva A, Cavalera MA, Gernone F, Nasar S, Ghergo P, Cordisco M, Corrente M, and Zatelli A
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- Animals, Cats, Dogs, Pilot Projects, Male, Cross-Sectional Studies, Female, Prevalence, Cat Diseases microbiology, Cat Diseases epidemiology, Bacteriuria veterinary, Bacteriuria microbiology, Bacteriuria epidemiology, Bacteremia veterinary, Bacteremia microbiology, Bacteremia epidemiology, Dog Diseases microbiology, Dog Diseases epidemiology, Renal Insufficiency, Chronic veterinary, Renal Insufficiency, Chronic complications, Renal Insufficiency, Chronic epidemiology, Renal Insufficiency, Chronic microbiology
- Abstract
In human medicine, major infections are the most significant and critical non-cardiovascular complications in patients affected by chronic kidney disease (CKD), with bacteriuria being the primary source of bloodstream infections and its evolution toward sepsis. The availability of data on prevalence of bacteremia and its association with bacteriuria in dogs and cats with CKD is limited. The aim of this observational cross-sectional study was to determine the occurrence of bacteremia, bacteriuria, and bacteriuria-related bacteremia in dogs and cats affected by CKD. Client-owned dogs and cats with a documented history of CKD undergoing disease follow-up were enrolled. Each included animal underwent a comprehensive physical examination, clinico-pathological and microbiological analyses of blood and urine, along with molecular detection of the 16S rRNA bacterial gene in blood. Aseptically collected blood and urine were obtained through jugular venipuncture and cystocentesis, respectively. After collection, blood and urine samples underwent bacteriological culture within one hour. In the population enrolled, 2/47 dogs and 1/41 cats presented bacteriemia. Moreover, 8/47 dogs and 6/41 cats presented a positive urine culture. Additionally, in one out of the 47 dogs, the same pathogen was identified from blood and urine samples, with a final diagnosis of urosepsis. No instances of bacteriuria-related bacteriemia were observed in the cat population. In conclusion, this study shows a low prevalence of bacteremia and confirms a high prevalence of bacteriuria in companion animals affected by CKD. Moreover, a low prevalence of bacteriuria-related bacteremia was also found., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)
- Published
- 2024
- Full Text
- View/download PDF
22. Transfusion reactions associated with COVID-19 convalescent plasma in outpatient clinical trials.
- Author
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Huaman MA, Raval JS, Paxton JH, Mosnaim GS, Patel B, Anjan S, Meisenberg BR, Levine AC, Marshall CE, Yarava A, Shenoy AG, Heath SL, Currier JS, Fukuta Y, Blair JE, Spivak ES, Petrini JR, Broderick PB, Rausch W, Cordisco M, Hammel J, Greenblatt B, Cluzet VC, Cruser D, Oei K, Abinante M, Hammitt LL, Sutcliffe CG, Forthal DN, Zand MS, Cachay ER, Kassaye SG, Ram M, Wang Y, Das P, Lane K, McBee NA, Gawad AL, Karlen N, Ford DE, Laeyendecker O, Pekosz A, Klein SL, Ehrhardt S, Lau B, Baksh SN, Shade DM, Casadevall A, Hanley DF, Ou J, Gniadek TJ, Ziman A, Shoham S, Gebo KA, Bloch EM, Tobian AAR, Sullivan DJ, and Gerber JM
- Subjects
- Humans, COVID-19 Serotherapy, Immunization, Passive adverse effects, Outpatients, SARS-CoV-2, Randomized Controlled Trials as Topic, COVID-19 therapy, COVID-19 etiology, Transfusion Reaction etiology, Urticaria etiology
- Abstract
Background: COVID-19 convalescent plasma (CCP) is an important therapeutic option for outpatients at high risk of hospitalization from SARS-CoV-2 infection. We assessed the safety of outpatient CCP transfusions administered during clinical trials., Study Design and Methods: We analyzed data pertaining to transfusion-related reactions from two randomized controlled trials in the U.S. that evaluated the efficacy of CCP versus control plasma in various ambulatory settings. Multivariable logistic regression was used to assess whether CCP was associated with transfusion reactions, after adjusting for potential confounders., Results: The combined study reported 79/1351 (5.9%) adverse events during the transfusion visit, with the majority 62/1351 (4.6%) characterized by mild, allergic-type findings of urticaria, and/or pruritus consistent with minor allergic transfusion reactions; the other reported events were attributed to the patients' underlying disease, COVID-19, or vasovagal in nature. We found no difference in the likelihood of allergic transfusion reactions between those receiving CCP versus control plasma (adjusted odds ratio [AOR], 0.75; 95% CI, 0.43-1.31). Risk of urticaria and/or pruritus increased with a pre-existing diagnosis of asthma (AOR, 2.33; 95% CI, 1.16-4.67). We did not observe any CCP-attributed antibody disease enhancement in participants with COVID-19 or increased risk of infection. There were no life-threatening severe transfusion reactions and no patients required hospitalization related to transfusion-associated complications., Discussion: Outpatient plasma administration was safely performed for nearly 1400 participants. CCP is a safe therapeutic option for outpatients at risk of hospitalization from COVID-19., (© 2023 The Authors. Transfusion published by Wiley Periodicals LLC on behalf of AABB.)
- Published
- 2023
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23. Antibacterial and Biofilm Production Inhibition Activity of Thymus vulgaris L. Essential Oil against Salmonella spp. Isolates from Reptiles.
- Author
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Galgano M, Mrenoshki D, Pellegrini F, Capozzi L, Cordisco M, Del Sambro L, Trotta A, Camero M, Tempesta M, Buonavoglia D, Laricchiuta P, Catella C, Pratelli A, Buonavoglia A, and Corrente M
- Abstract
Salmonellosis is an infectious disease affecting both animals and humans. Antimicrobial resistant (AMR) and biofilm-producing Salmonella spp., frequently detected in reptiles (who can then act as asymptomatic carriers for warm-blooded animals), have developed resistance to biocides; this represents a warning for the emergence of biocide/antimicrobial cross-resistance. The aim of this study was to evaluate the efficacy of Thymus vulgaris L. essential oil (TEO) in inhibiting bacterial growth and biofilm production of Salmonella spp., which had been isolated from wild reptiles housed in a Zoo in Italy. The resistance profile against different classes of antibiotics showed that all the isolates were susceptible to the tested antibiotics, despite the presence of several AMR genes. All the isolates were also tested with aqueous solutions of TEO at different dilutions (5% to 0.039%). Interestingly, TEO proved effective both in inhibiting bacterial growth at low dilutions, with MIC and MBC values ranging between 0.078% and 0.312%, and in inhibiting biofilm production, with values ranging from 0.039% to 0.156%. TEO demonstrated effective bioactivity against the biofilm producer Salmonella spp., proving to be a valid disinfectant for the prevention of salmonellosis from reptiles, a possible source of infection for humans exposed to the reptiles' environment.
- Published
- 2023
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24. Evaluation of antibacterial oxygen/ozone mixture in vitro activity on bacteria isolated from cervico-vaginal mucus of cows with acute metritis.
- Author
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Lillo E, Cordisco M, Trotta A, Greco G, Carbonari A, Rizzo A, Sciorsci RL, and Corrente M
- Subjects
- Cattle, Animals, Female, Oxygen pharmacology, Escherichia coli, Staphylococcus aureus, Pilot Projects, Ozone pharmacology
- Abstract
Ozone is an oxidating gas showing a strong microbicidal activity on bacteria, fungi, viruses and protozoa. The aim of this study was to test the in vitro bacteriocidal action of an Ozone/Oxygen gas mixture on bacteria isolated from the cervico-vaginal mucus of cows affected by acute metritis. A pilot study was initially carried out on reference strains (Escherichia coli ATCC 25922, Staphylococcus aureus ATCC 25923 and Mycoplasma bovigenitalium ATCC 19852) that were tested with three different treatments: a control positive baseline group (B-group) was incubated without gas treatment, a control positive oxygen group (O
2 -group) was treated with pure oxygen 100%, and the treated group (T-group) was exposed to a gaseous constant flow of an Ozone/Oxygen mixture, at 50, 35, 20 μg Ozone/ml and for 5, 3 and 1 min for every different Ozone concentration. In both positive control groups, the number of colony forming units (CFU) per ml was higher than 300 CFU/ml (E. coli and S. aureus) and higher than 30 CFU/ml for M. bovigenitalium, after incubation. The T-groups showed a minimal bacterial growth equal to or lower than 1 CFU/ml per plate. Based on the results of the pilot study, a second phase was performed on bacteria isolated from the cervico-vaginal mucus (Klebsiella pneumoniae, Enterobacter agglomerans, E. coli, Proteus mirabilis and M. bovigenitalium) using the lower concentration of 20 μg/ml of Ozone for the minimum exposure time of 1 min. The E. coli and S. aureus reference strains and the clinical isolates (K. pneumoniae, E. agglomerans, E. coli, P. mirabilis) were incubated at 37 °C for 48 h and the colonies were manually counted at 24 h and 48 h following inoculation. The cultures of M. bovigenitalium (both ATCC and clinical isolate) were incubated in a jar with modified atmosphere conditions with 5% CO2 at 37 °C for 4-7 days and colony counting was performed. The second phase showed a low number of CFUs (equal to or less than 7 CFU/ml) for the clinical isolates K. pneumoniae, E. agglomerans, E. coli and P. mirabilis, and, of note, for M. bovigenitalium, both ATCC and clinical isolate, the growth was completely inhibited. Ozone was demonstrated to have a bacteriocidal activity. This study encourages further research of in vivo application of low doses of gaseous Ozone for the treatment of metritis in cows by using minimal exposure times., (Copyright © 2022 Elsevier Inc. All rights reserved.)- Published
- 2023
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25. Prevalence of bacteriuria in cats with neurogenic bladder.
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Uva A, Gernone F, Cavalera MA, Carelli G, Cordisco M, Trotta A, Donghia R, Corrente M, and Zatelli A
- Subjects
- Animals, Cats, Prevalence, Prospective Studies, Bacteriuria epidemiology, Bacteriuria veterinary, Bacteriuria diagnosis, Cat Diseases epidemiology, Cat Diseases diagnosis, Renal Insufficiency, Chronic veterinary, Urinary Bladder, Neurogenic complications, Urinary Bladder, Neurogenic epidemiology, Urinary Bladder, Neurogenic veterinary
- Abstract
Urinary tract infections are defined as the adherence, multiplication, and persistence of an infectious agent within the urogenital system, causing an associated inflammatory response and clinical signs; instead, the presence of bacteria in urine as determined by positive bacterial culture (PUC) from a properly collected urine specimen, in the absence of clinical signs, is defined subclinical bacteriuria. Limited information on the prevalence of PUC in spinal cord injury cats affected by neurogenic bladder (NB) is available. On contrary, in NB dogs and humans the prevalence of bacteriuria is well documented. Moreover, while in humans information about bacteriemia associated with NB is already available, this aspect has never been studied in NB cats. The aim of this prospective study was to determine the prevalence of PUC in cats with NB, compared to animals affected by chronic kidney disease (CKD) and healthy cats. Furthermore, the prevalence of bacteriemia in cats with NB was evaluated. Fifty-one cats met the inclusion criteria: 12 cats were affected by NB, 22 had CKD and 17 were healthy. The prevalence of PUC was 58.33% and 18% in NB and CKD cat populations, respectively. All blood cultures were negative. The incomplete bladder emptying and the decreased resistance in the bladder wall could be considered predisposing elements to PUC in the NB feline population. The results of this study highlight, for the first time, an high prevalence of PUC in cats affected by NB, which was not found to be associated with bacteriemia., (© 2022. The Author(s), under exclusive licence to Springer Nature B.V.)
- Published
- 2022
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26. Antimicrobial Activity of Essential Oils Evaluated In Vitro against Escherichia coli and Staphylococcus aureus .
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Galgano M, Capozza P, Pellegrini F, Cordisco M, Sposato A, Sblano S, Camero M, Lanave G, Fracchiolla G, Corrente M, Cirone F, Trotta A, Tempesta M, Buonavoglia D, and Pratelli A
- Abstract
The spread of extended-spectrum β-lactamase-producing Escherichia coli and methicillin-resistant Staphylococcus aureus has caused a reduction in antibiotic effectiveness and an increase in mortality rates. Essential oils (EOs), known for their therapeutic efficacy, can be configured as novel broad-spectrum biocides. Accordingly, the bacteriostatic-bactericidal activity of Citrus Lemon (LEO), Pinus Sylvestris (PEO), Foeniculum Vulgaris (FEO), Ocimum Basilicum (BEO), Melissa Officinalis (MEO), Thymus Vulgaris (TEO), and Zingiber Officinalis Rosc. (GEO), at concentrations ranging from 1.25 to 40% ( v / v ), were tested in vitro against different E. coli and S. aureus strains using minimal inhibitory concentrations (MICs) and minimum bactericidal concentrations (MBCs). The chemical compositions of the EOs were analyzed using GC/MS. The major components of all seven tested oils were limonene, α-pinene, anethole, estragole, citral, thymol, and zingiberene, respectively. We found that the bacteriostatic-bactericidal activity of the EOs was related to their chemotypes and concentrations, as well as the strain of the bacteria. A dose-effect correlation was found when testing GEO against S. aureus strains , whilst FEO was found to have no activity regardless of concentration. PEO, MEO, and BEO were found to have bactericidal effect with a MIC and MBC of 1.25% ( v / v ) against S. aureus strains, and LEO was found to have values of 1.25% ( v / v ) and 5% ( v / v ) against ATCC and clinical isolate, respectively. Interestingly, the antimicrobial activity of TEO was not related to oil concentration and the complete inhibition of growth across all E. coli and S. aureus was observed. Although preliminary, our data demonstrate the efficacy of EOs and pave the way for further investigations on their potential synergistic use with traditional drugs in the human and veterinary fields.
- Published
- 2022
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27. Canine Parainfluenza Virus Infection in a Dog with Acute Respiratory Disease.
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Cordisco M, Lucente MS, Sposato A, Cardone R, Pellegrini F, Franchini D, Di Bello A, and Ciccarelli S
- Abstract
The canine infectious respiratory disease complex (CIRDC) is an endemic respiratory syndrome caused by different bacterial and viral pathogens. This report describes a case of canine parainfluenza virus infection in a vaccinated household dog with an acute respiratory symptom (dry cough), who underwent clinical and endoscopic investigations for a suspected foreign body. Cytological investigations carried out on the broncho-alveolar lavage fluid (BALF) tested negative for the presence of inflammatory or infectious processes and could have been misleading the clinicians. By the molecular analyses (PCR) carried out on the BALF, canine parainfluenza virus was exclusively detected without the simultaneous presence of other respiratory pathogens associated to CIRDC. This case report emphasizes the role of molecular diagnostics in the differential diagnosis of respiratory diseases, in order to avoid underestimating the circulation of the parainfluenza virus in the canine population.
- Published
- 2022
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28. Alveolar osteitis associated with methicillin-resistant Staphylococcus epidermidis.
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Buonavoglia A, Trotta A, Cordisco M, Zamparini F, Corrente M, and Prati C
- Subjects
- Adult, Anti-Bacterial Agents pharmacology, Anti-Bacterial Agents therapeutic use, Azithromycin, Female, Humans, Methicillin Resistance genetics, Microbial Sensitivity Tests, Staphylococcus epidermidis genetics, Dry Socket drug therapy, Dry Socket etiology, Methicillin-Resistant Staphylococcus aureus, Staphylococcal Infections microbiology
- Abstract
A critical point in dentistry is the empiric prescription of broad-spectrum antibiotics that could increase the levels of antimicrobial resistance. Alveolar osteitis is one of the most common post-op- erative complications in which antibiotic use is controversial. A 35-year-old female, with pain in the right mandibular region and treated with cefixime, was diagnosed with cracked tooth syndrome and pulpitis. The tooth was extracted and a massive purulent bleeding drainage was observed. Irrigation of the socket and a new therapy with azithromycin were done. Bacteriological analysis, a specific mecA gene PCR for the methicillin resistance, and the antimicrobial susceptibility test were per- formed on the bacterial isolate. A Staphylococcus epidermidis isolate was methicillin-resistant and showed resistance to erythromycin, azithromycin, clarithromycin, and sulfamethoxazole + trimeth- oprim. After 7 days, intraoral examination showed a complete resolution. The aim of this report is to suggest that systemic antibiotics may provide insufficient efficacy during alveolar osteitis, especially when caused by a multidrug-resistant organism.
- Published
- 2022
29. Multidrug resistant Enterococcus faecium isolate from cholangitis/cholecystitis in a dog.
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Sposato A, Cordisco M, de Ruvo G, Ferro S, Raineri RA, Trotta A, Buonavoglia D, and Corrente M
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- Animals, Dogs, Cholangitis veterinary, Cholecystitis veterinary, Dog Diseases pathology, Enterococcus faecium, Mucocele pathology, Mucocele surgery, Mucocele veterinary
- Abstract
Mucocele and cholecystitis were diagnosed in a 10 year-old Shetland-sheepdog presenting aspecific clinical signs. Blood examinations and ultrasonography investigation were performed before to surgical approach, which allowed to collect biopsies and samples for bacteriological analyses. In addition, the patient was subjected to cholecystectomy. A multidrug resistant Enterococcus faecium was isolated from the gallbladder specimens. On the basis of antimicrobial susceptibility test, nitrofurantoin was used. The correct bacteriological diagnosis is necessary to set up effective therapy, influencing the patient's prognosis and improving the recovery time., (© 2022 The Authors. Veterinary Medicine and Science published by John Wiley & Sons Ltd.)
- Published
- 2022
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30. African Swine Fever-How to Unravel Fake News in Veterinary Medicine.
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Trotta A, Marinaro M, Cavalli A, Cordisco M, Piperis A, Buonavoglia C, and Corrente M
- Abstract
In recent years, fake scientific news has spread much faster through the Internet and social media within the so-called "infodemic". African Swine Fever (ASF) is a perfect case study to prove how fake news can undermine the public health response, even in the veterinary field. ASF is a highly contagious infective disease affecting exclusively domestic and wild pigs such as wild boars. ASF can cause social damage and economic losses both directly (due to the high mortality rate) and indirectly (due to international sanctions). Although ASF is not a threat to human health, since 2018 newspapers have often reported false or misleading news, ranging from misinterpreted findings/data to fake or alarmistic news. In some cases, fake news was spread, such as the use of snipers at the border of nations to kill wild boars, or those reports concerning possible risks to human health. In order to provide real and fact-based news on epidemics, some organizations have created easy-to-read infographic and iconographic materials, available on their websites, to help the readers identifying the fake news. Indeed, it is crucial that governments and scientific organizations work against fear and anxiety, using simple and clear communication.
- Published
- 2022
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31. Bayesian estimation of prevalence of Johne's disease in dairy herds in Southern Italy.
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Sposato A, Fanelli A, Cordisco M, Trotta A, Galgano M, Corrente M, and Buonavoglia D
- Subjects
- Animals, Bayes Theorem, Cattle, Dairying, Enzyme-Linked Immunosorbent Assay veterinary, Italy epidemiology, Prevalence, Cattle Diseases epidemiology, Cattle Diseases microbiology, Paratuberculosis epidemiology
- Abstract
Johne's disease (JD) is a chronic granulomatous disease caused by Mycobacterium avium subsp. paratuberculosis (MAP) causing important losses on dairy farms. In Italy, voluntary programs to control MAP infection in dairy cattle are implemented in the Northern part of the country, where several studies have been carried out. Conversely, the disease status has not been fully investigated in the Southern regions. The aims of this study were to (i) determine the herd-level true prevalence (HTP) and (ii) the conditional within herd animal-level prevalence (CWHP) of JD in selected dairy cattle herds in Southern Italy. Serum samples were taken from 27 farms and analysed using a commercial ELISA test. A Bayesian model was fitted to the data. The estimated posterior mean of HPT was 0.46 (89 % CI 0.25-0.67), while the mean CWHP was 0.03 (89 % CI: 0.012-0.045). The results presented in this study call for designing and implementing an effective JD control program at national level., (Copyright © 2021 Elsevier B.V. All rights reserved.)
- Published
- 2022
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32. A Young Boy With Hemophagocytic Lymphohistiocytosis Presenting With Vaccine-Related Granulomatous Dermatitis: A Case Report and Literature Review.
- Author
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Zengin HB, Reyes-Barron C, Cusick E, Cordisco M, Katzman PJ, Burack WR, and Scott G
- Subjects
- Child, Preschool, Dermatitis pathology, Granuloma pathology, Humans, Lymphohistiocytosis, Hemophagocytic genetics, Male, Mutation, Drug Eruptions genetics, Lymphohistiocytosis, Hemophagocytic complications, Membrane Proteins genetics, Vaccines adverse effects
- Abstract
Abstract: Cutaneous eruptions associated with hemophagocytic lymphohistiocytosis (HLH) have been reported in 6%-63% of patients. Clinical findings of these skin lesions vary widely and include maculopapular rashes, ulcers, and violaceous nodules. Corresponding histologic findings are also variable and are considered nonspecific. We report the case of a 4-year-old boy who initially developed a widespread popular-pustular rash 2 weeks after his 12-month measles, mumps, and rubella vaccinations. These resolved with scarring then recurred following his 24-month vaccinations. Multiple skin biopsies were negative for infectious organisms and showed a granulomatous infiltrate with perforation and necrobiosis. The differential diagnosis included perforating granuloma annulare, infection, or rheumatoid nodules. At the age of 4, he developed fever, hepatosplenomegaly, pancytopenia and other laboratory abnormalities, requiring hospitalization. A number of studies were performed including biopsies of bone marrow and liver. Molecular testing revealed 2 mutations in UNC13D known to be associated with familial HLH. His prior cutaneous lesions were likely caused by immune dysregulation exacerbated by immunizations because of underlying familial HLH. This case illustrates the importance of recognizing an unusual cutaneous manifestation of a rare disease to arrive at an earlier diagnosis in a pediatric patient. Although cutaneous eruptions usually develop concurrently with other systemic symptoms of HLH, preceding unusual skin lesions may be the first indication of this rare disease., Competing Interests: The authors declare no conflicts of interest., (Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.)
- Published
- 2021
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33. Natural Bovine Coronavirus Infection in a Calf Persistently Infected with Bovine Viral Diarrhea Virus: Viral Shedding, Immunological Features and S Gene Variations.
- Author
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Pratelli A, Lucente MS, Cordisco M, Ciccarelli S, Di Fonte R, Sposato A, Mari V, Capozza P, Pellegrini F, Carelli G, Azzariti A, and Buonavoglia C
- Abstract
The evolution of a bovine coronavirus (BCoV) natural infection in a calf persistently infected with bovine viral diarrhea virus (BVDV) was described. The infected calf developed intermittent nasal discharge, diarrhea and hyperthermia. The total number of leukocytes/mL and the absolute differential number of neutrophils and lymphocytes resulted within the normal range, but monocytes increased at T28 (time 28 post-infection). Flow-cytometry analysis evidenced that the CD8
+ subpopulation increased at T7 and between T28 and T35. BCoV shedding in nasal discharges and feces was detected up to three weeks post infection and high antibody titers persisted up to T56. The RNA BCoV load increased until T14, contrary to what was observed in a previous study where the fecal excretion of BCoV was significantly lower in the co-infected (BCoV/BVDV) calves than in the calves infected with BCoV only. We can suppose that BVDV may have modulated the BCoV infection exacerbating the long viral excretion, as well as favoring the onset of mutations in the genome of BCoV detected in fecal samples at T21. An extensive study was performed to verify if the selective pressure in the S gene could be a natural mode of variation of BCoV, providing data for the identification of new epidemic strains, genotypes or recombinant betacoronaviruses .- Published
- 2021
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34. HPV Vaccination Status and Resolution of Warts in Pediatric Patients.
- Author
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Burli A, Hancock S, Zhao YT, Paul D, and Cordisco M
- Abstract
Background: Warts are a common dermatologic complaint with an increased incidence within the pediatric population. Warts are caused by multiple strains of the human papillomavirus (HPV). There is little research on how a patient's HPV immunization status affects the response to treatment of warts in pediatric patients., Aims: The purpose of this study is to investigate the relationship between HPV vaccination status and wart resolution., Materials and Methods: This is a retrospective chart review that investigates the relationship between response to routine treatment of warts and a subject's HPV vaccination status., Results: There was no significant relationship found between HPV vaccination status and resolution of warts ( p = 0.797). However, there was a significant positive correlation between having the HPV vaccine and number of visits for the treatment of warts ( r = 0.180, P = 0.024)., Conclusion: This study did not show a significant correlation between HPV vaccination status and wart resolution, although it demonstrated a significant positive relationship between those immunized with the HPV vaccine and an increased number of treatment visits. Possible explanations for this unexpected correlation include the variation in HPV vaccine formulation, vaccination status, and frequency of office visits, since vaccinated patients are more likely to be compliant with office visits., Competing Interests: There are no conflicts of interest., (Copyright: © 2022 Indian Journal of Dermatology.)
- Published
- 2021
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35. A simple pooling salivary test for SARS-CoV-2 diagnosis: A Columbus' egg?
- Author
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Pratelli A, Lucente MS, Mari V, Cordisco M, Sposato A, Capozza P, Lanave G, Martella V, and Buonavoglia A
- Subjects
- COVID-19 virology, COVID-19 Nucleic Acid Testing economics, Humans, Limit of Detection, Reagent Strips analysis, SARS-CoV-2 genetics, Saliva virology, COVID-19 diagnosis, COVID-19 Nucleic Acid Testing methods, Coronavirus, Bovine genetics, Genome, Viral, RNA, Viral genetics, Specimen Handling methods
- Abstract
Saliva is an appropriate specimen for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) diagnosis. The possibility of pooling samples of saliva, using non-invasive bibula strips for sampling, was explored employing Bovine coronavirus (BCoV) spiked saliva. In laboratory, up to 30 saliva-soaked strips were pooled in a single tube with 2 mL of medium. After quick adsorption with the medium and vortexing, the liquid was collected and tested with a quantitative molecular assay to quantify viral RNA genome copies. On testing of single and pooled strips, the difference between the median threshold cycles (Ct) value of test performed on the single positive saliva sample and the median Ct value obtained on the pool of 30 strips, was 3.21 cycles. Saliva pooling with bibula strips could allow monitoring of COVID-19 on a large scale, reducing costs for the health bodies in terms of medical material and skilled personnel. Finally, saliva sampling is noninvasive and less traumatic than nasopharyngeal swabs and can be self-collected., (Copyright © 2021. Published by Elsevier B.V.)
- Published
- 2021
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36. Thrombolysis in elderly stroke patients in Italy (TESPI) trial and updated meta-analysis of randomized controlled trials.
- Author
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Lorenzano S, Vestri A, Lancia U, Bovi P, Cappellari M, Stanzione P, Samà D, Bruscoli M, Cavazzuti M, Zini A, Rasura M, Beccia M, Comi G, Sessa M, Gandolfo C, Balestrino M, Agnelli G, Caso V, Gerbino Promis P, Pozzessere C, Anticoli S, Perini F, Marcon M, Vinattieri A, Caruso A, Magoni M, Furlan M, Orlandi G, Di Lazzaro V, Valente M, Nencini P, Cordisco M, Verna R, and Toni D
- Subjects
- Aged, Fibrinolytic Agents therapeutic use, Humans, Italy, Multicenter Studies as Topic, Randomized Controlled Trials as Topic, Thrombolytic Therapy, Tissue Plasminogen Activator therapeutic use, Treatment Outcome, Brain Ischemia complications, Brain Ischemia drug therapy, Stroke drug therapy
- Abstract
Background: Since its approval, the use of alteplase had been limited to patients aged ≤80 years., Aims: TESPI trial had been designed to evaluate whether alteplase treatment within 3 h in patients with acute ischemic stroke aged >80 years resulted in favorable benefit/risk ratio compared with standard care. The meta-analysis of randomized controlled trials was updated to put findings in the context of all available evidence., Methods: TESPI was a multicenter, open-label with blinded outcome evaluation, randomized, controlled trial. Main clinical endpoints were 90-day favorable functional outcome (mRS score 0-2) and mortality and symptomatic intracerebral hemorrhage. The trial was prematurely terminated for ethical reasons after publication of IST-3 trial which provided evidence of treatment benefit in elderly., Results: Of the planned 600 patients, 191 (88 assigned to alteplase) were enrolled. Overall, 24/83 (28.9%) alteplase patients had a favorable outcome compared to 22/95 (23.2%) controls (non-significant absolute difference of 5.7% for alteplase; OR 1.35, 95% CI 0.69-2.64, P = 0.381). Rates of death were non-significantly lower in the alteplase patients (18.1% vs. 26.5%); rates of symptomatic intracerebral hemorrhage were similar between the two groups (5.9% vs. 5.1%). The updated meta-analysis showed consistent results with prior estimates and add weights., Conclusions: The effects of alteplase observed in this interrupted trial did not reach statistical significance, probably for the small numbers, but are consistent with and add weight to the sum total of the randomized evidence demonstrating that alteplase is beneficial in patients with acute ischemic stroke aged over 80 years, particularly if given within 3 h.
- Published
- 2021
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37. Unrelenting facial segmental hemangiomas: A case series of late growth and recurrent ulcerations.
- Author
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Fernandez Faith E and Cordisco M
- Subjects
- Face, Humans, Infant, Syndrome, Hemangioma complications, Hemangioma diagnosis, Vascular Malformations
- Abstract
Late growth of infantile hemangiomas is an uncommon complication. We report three patients with segmental facial hemangiomas who experienced late growth and recurrent ulceration predominantly of the lower lip. These patients shared common clinical features including involvement of the S3 facial segment, oral and airway hemangiomas, and vascular anomalies associated with PHACE syndrome. This report highlights a clinical presentation at-risk for late growth and recurrent ulceration., (© 2020 Wiley Periodicals LLC.)
- Published
- 2020
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38. A nodular growth arising on a linear lesion in an adolescent.
- Author
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Bawany F, Paul D, Morrison C, Scott GA, and Cordisco M
- Subjects
- Adolescent, Diagnosis, Differential, Humans, Fasciitis
- Published
- 2020
- Full Text
- View/download PDF
39. Enlarging facial soft tissue mass in an infant.
- Author
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Agnihothri R, Katzman PJ, Morrison CS, and Cordisco M
- Subjects
- Biopsy, Needle, Contrast Media, Diagnosis, Differential, Fasciitis diagnostic imaging, Follow-Up Studies, Forehead, Humans, Immunohistochemistry, Infant, Male, Sarcoma diagnostic imaging, Treatment Outcome, Ultrasonography, Doppler methods, Fasciitis pathology, Fasciitis surgery, Magnetic Resonance Imaging methods, Sarcoma pathology, Sarcoma surgery, Skin pathology
- Published
- 2019
- Full Text
- View/download PDF
40. Guttate leukoderma in a 7-year-old girl.
- Author
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Shah PR, Esaa FS, Scott G, and Cordisco M
- Subjects
- Child, Female, Humans, Immunosuppressive Agents therapeutic use, Lichen Sclerosus et Atrophicus drug therapy, Tacrolimus therapeutic use, Lichen Sclerosus et Atrophicus pathology
- Published
- 2019
- Full Text
- View/download PDF
41. Prenatal Risk Factors for PHACE Syndrome: A Study Using the PHACE Syndrome International Clinical Registry and Genetic Repository.
- Author
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Wan J, Steiner J, Baselga E, Blei F, Cordisco M, Garzon MC, Goddard DS, Haggstrom A, Krol A, Frieden IJ, Metry D, Morel KD, Verhagen JMA, Wargon O, Drolet BA, and Siegel DH
- Subjects
- Aortic Coarctation epidemiology, Cross-Sectional Studies, Eye Abnormalities epidemiology, Female, Humans, Infant, Newborn, Male, Neurocutaneous Syndromes epidemiology, Placenta Previa, Pre-Eclampsia, Pregnancy, Prenatal Care statistics & numerical data, Registries, Risk Factors, United States epidemiology, Aortic Coarctation etiology, Eye Abnormalities etiology, Neurocutaneous Syndromes etiology
- Abstract
The cause of PHACE syndrome is unknown. In a study of 218 patients, we examined potential prenatal risk factors for PHACE syndrome. Rates of pre-eclampsia and placenta previa in affected individuals were significantly greater than in the general population. No significant risk factor differences were detected between male and female subjects., (Copyright © 2017 Elsevier Inc. All rights reserved.)
- Published
- 2017
- Full Text
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42. Germline Loss-of-Function Mutations in EPHB4 Cause a Second Form of Capillary Malformation-Arteriovenous Malformation (CM-AVM2) Deregulating RAS-MAPK Signaling.
- Author
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Amyere M, Revencu N, Helaers R, Pairet E, Baselga E, Cordisco M, Chung W, Dubois J, Lacour JP, Martorell L, Mazereeuw-Hautier J, Pyeritz RE, Amor DJ, Bisdorff A, Blei F, Bombei H, Dompmartin A, Brooks D, Dupont J, González-Enseñat MA, Frieden I, Gérard M, Kvarnung M, Hanson-Kahn AK, Hudgins L, Léauté-Labrèze C, McCuaig C, Metry D, Parent P, Paul C, Petit F, Phan A, Quere I, Salhi A, Turner A, Vabres P, Vicente A, Wargon O, Watanabe S, Weibel L, Wilson A, Willing M, Mulliken JB, Boon LM, and Vikkula M
- Subjects
- Databases, Genetic, Female, Genome-Wide Association Study methods, Humans, Male, Pedigree, Arteriovenous Malformations diagnosis, Arteriovenous Malformations genetics, Capillaries abnormalities, Germ-Line Mutation genetics, MAP Kinase Signaling System physiology, Port-Wine Stain diagnosis, Port-Wine Stain genetics, Receptor, EphB4 genetics, p120 GTPase Activating Protein genetics
- Abstract
Background: Most arteriovenous malformations (AVMs) are localized and occur sporadically. However, they also can be multifocal in autosomal-dominant disorders, such as hereditary hemorrhagic telangiectasia and capillary malformation (CM)-AVM. Previously, we identified RASA1 mutations in 50% of patients with CM-AVM. Herein we studied non-RASA1 patients to further elucidate the pathogenicity of CMs and AVMs., Methods: We conducted a genome-wide linkage study on a CM-AVM family. Whole-exome sequencing was also performed on 9 unrelated CM-AVM families. We identified a candidate gene and screened it in a large series of patients. The influence of several missense variants on protein function was also studied in vitro., Results: We found evidence for linkage in 2 loci. Whole-exome sequencing data unraveled 4 distinct damaging variants in EPHB4 in 5 families that cosegregated with CM-AVM. Overall, screening of EPHB4 detected 47 distinct mutations in 54 index patients: 27 led to a premature stop codon or splice-site alteration, suggesting loss of function. The other 20 are nonsynonymous variants that result in amino acid substitutions. In vitro expression of several mutations confirmed loss of function of EPHB4. The clinical features included multifocal CMs, telangiectasias, and AVMs., Conclusions: We found EPHB4 mutations in patients with multifocal CMs associated with AVMs. The phenotype, CM-AVM2, mimics RASA1 -related CM-AVM1 and also hereditary hemorrhagic telangiectasia. RASA1 -encoded p120RASGAP is a direct effector of EPHB4. Our data highlight the pathogenetic importance of this interaction and indicts EPHB4-RAS-ERK signaling pathway as a major cause for AVMs., (© 2017 American Heart Association, Inc.)
- Published
- 2017
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43. Blue Rubber Bleb Nevus (BRBN) Syndrome Is Caused by Somatic TEK (TIE2) Mutations.
- Author
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Soblet J, Kangas J, Nätynki M, Mendola A, Helaers R, Uebelhoer M, Kaakinen M, Cordisco M, Dompmartin A, Enjolras O, Holden S, Irvine AD, Kangesu L, Léauté-Labrèze C, Lanoel A, Lokmic Z, Maas S, McAleer MA, Penington A, Rieu P, Syed S, van der Vleuten C, Watson R, Fishman SJ, Mulliken JB, Eklund L, Limaye N, Boon LM, and Vikkula M
- Subjects
- Belgium, Cohort Studies, Female, Gastrointestinal Neoplasms diagnosis, Humans, Incidence, Male, Nevus, Blue diagnosis, Rare Diseases, Skin Neoplasms diagnosis, Vascular Malformations diagnosis, Gastrointestinal Neoplasms genetics, Genetic Predisposition to Disease epidemiology, Mutation, Nevus, Blue genetics, Receptor, TIE-2 genetics, Skin Neoplasms genetics, Vascular Malformations genetics
- Abstract
Blue rubber bleb nevus syndrome (Bean syndrome) is a rare, severe disorder of unknown cause, characterized by numerous cutaneous and internal venous malformations; gastrointestinal lesions are pathognomonic. We discovered somatic mutations in TEK, the gene encoding TIE2, in 15 of 17 individuals with blue rubber bleb nevus syndrome. Somatic mutations were also identified in five of six individuals with sporadically occurring multifocal venous malformations. In contrast to common unifocal venous malformation, which is most often caused by the somatic L914F TIE2 mutation, multifocal forms are predominantly caused by double (cis) mutations, that is, two somatic mutations on the same allele of the gene. Mutations are identical in all lesions from a given individual. T1105N-T1106P is recurrent in blue rubber bleb nevus, whereas Y897C-R915C is recurrent in sporadically occurring multifocal venous malformation: both cause ligand-independent activation of TIE2, and increase survival, invasion, and colony formation when expressed in human umbilical vein endothelial cells., (Copyright © 2016 The Authors. Published by Elsevier Inc. All rights reserved.)
- Published
- 2017
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44. PIK3CA -associated developmental disorders exhibit distinct classes of mutations with variable expression and tissue distribution.
- Author
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Mirzaa G, Timms AE, Conti V, Boyle EA, Girisha KM, Martin B, Kircher M, Olds C, Juusola J, Collins S, Park K, Carter M, Glass I, Krägeloh-Mann I, Chitayat D, Parikh AS, Bradshaw R, Torti E, Braddock S, Burke L, Ghedia S, Stephan M, Stewart F, Prasad C, Napier M, Saitta S, Straussberg R, Gabbett M, O'Connor BC, Keegan CE, Yin LJ, Lai AHM, Martin N, McKinnon M, Addor MC, Boccuto L, Schwartz CE, Lanoel A, Conway RL, Devriendt K, Tatton-Brown K, Pierpont ME, Painter M, Worgan L, Reggin J, Hennekam R, Tsuchiya K, Pritchard CC, Aracena M, Gripp KW, Cordisco M, Van Esch H, Garavelli L, Curry C, Goriely A, Kayserilli H, Shendure J, Graham J Jr, Guerrini R, and Dobyns WB
- Subjects
- Female, Genetic Association Studies, High-Throughput Nucleotide Sequencing, Humans, Infant, Male, Mutation, Phenotype, Tissue Distribution, Class I Phosphatidylinositol 3-Kinases genetics, Malformations of Cortical Development genetics, Mosaicism, Vascular Malformations genetics
- Abstract
Mosaicism is increasingly recognized as a cause of developmental disorders with the advent of next-generation sequencing (NGS). Mosaic mutations of PIK3CA have been associated with the widest spectrum of phenotypes associated with overgrowth and vascular malformations. We performed targeted NGS using 2 independent deep-coverage methods that utilize molecular inversion probes and amplicon sequencing in a cohort of 241 samples from 181 individuals with brain and/or body overgrowth. We identified PIK3CA mutations in 60 individuals. Several other individuals ( n = 12) were identified separately to have mutations in PIK3CA by clinical targeted-panel testing ( n = 6), whole-exome sequencing ( n = 5), or Sanger sequencing ( n = 1). Based on the clinical and molecular features, this cohort segregated into three distinct groups: (a) severe focal overgrowth due to low-level but highly activating (hotspot) mutations, (b) predominantly brain overgrowth and less severe somatic overgrowth due to less-activating mutations, and (c) intermediate phenotypes (capillary malformations with overgrowth) with intermediately activating mutations. Sixteen of 29 PIK3CA mutations were novel. We also identified constitutional PIK3CA mutations in 10 patients. Our molecular data, combined with review of the literature, show that PIK3CA -related overgrowth disorders comprise a discontinuous spectrum of disorders that correlate with the severity and distribution of mutations.
- Published
- 2016
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45. Copy number variation analysis in 98 individuals with PHACE syndrome.
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Siegel DH, Shieh JTC, Kwon EK, Baselga E, Blei F, Cordisco M, Dobyns WB, Duffy KJ, Garzon MC, Gibbs DL, Grimmer JF, Hayflick SJ, Krol AL, Kwok PY, Lorier R, Matter A, McWeeney S, Metry D, Mitchell S, Pope E, Santoro JL, Stevenson DA, Bayrak-Toydemir P, Wilmot B, Worthey EA, Frieden IJ, Drolet BA, and Broeckel U
- Subjects
- Adolescent, Adult, Case-Control Studies, Child, Child, Preschool, Female, Genotyping Techniques, Humans, Infant, Male, Reproducibility of Results, Signal Transduction, Young Adult, Aortic Coarctation genetics, DNA genetics, DNA Copy Number Variations genetics, Eye Abnormalities genetics, Neurocutaneous Syndromes genetics
- Abstract
PHACE syndrome is the association of large segmental facial hemangiomas and congenital anomalies, such as posterior fossa malformations, cerebral arterial anomalies, coarctation of the aorta, eye anomalies, and sternal defects. To date, the reported cases of PHACE syndrome have been sporadic, suggesting that PHACE may have a complex pathogenesis. We report here genomic copy number variation (CNV) analysis of 98 individuals with PHACE syndrome as a first step in deciphering a potential genetic basis of PHACE syndrome. A total of 3,772 CNVs (2,507 duplications and 1,265 deletions) were detected in 98 individuals with PHACE syndrome. CNVs were then eliminated if they failed to meet established criteria for quality, spanned centromeres, or did not contain genes. CNVs were defined as "rare" if not documented in the database of genomic variants. Ten rare CNVs were discovered (size range: 134-406 kb), located at 1q32.1, 1q43, 3q26.32-3q26.33, 3p11.1, 7q33, 10q24.32, 12q24.13, 17q11.2, 18p11.31, and Xq28. There were no rare CNV events that occurred in more than one subject. Therefore, further study is needed to determine the significance of these CNVs in the pathogenesis of PHACE syndrome.
- Published
- 2013
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- View/download PDF
46. Stroke in children with posterior fossa brain malformations, hemangiomas, arterial anomalies, coarctation of the aorta and cardiac defects, and eye abnormalities (PHACE) syndrome: a systematic review of the literature.
- Author
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Siegel DH, Tefft KA, Kelly T, Johnson C, Metry D, Burrows P, Pope E, Cordisco M, Holland KE, Maheshwari M, Keith P, Garzon M, Hess C, Frieden IJ, Fullerton HJ, and Drolet BA
- Subjects
- Angiography methods, Aortic Coarctation complications, Aortic Coarctation diagnostic imaging, Brain abnormalities, Cohort Studies, Eye Abnormalities complications, Eye Abnormalities diagnostic imaging, Female, Heart Defects, Congenital complications, Heart Defects, Congenital diagnostic imaging, Hemangioma complications, Hemangioma diagnostic imaging, Humans, Infant, Male, Risk Factors, Syndrome, Abnormalities, Multiple diagnostic imaging, Stroke diagnostic imaging, Stroke etiology
- Abstract
Background and Purpose: PHACE is an acronym for posterior fossa brain malformations, hemangiomas, arterial anomalies, coarctation of the aorta and cardiac defects, and eye abnormalities. Several case reports of arterial ischemic stroke (AIS) in individuals with PHACE have been published, but risk factors for AIS in PHACE have not been clearly defined. The objective of this article is to review all cases of stroke in PHACE in children and describe clinical characteristics that may be associated with an increased risk of AIS., Methods: A literature and registry search was conducted to identify patients with PHACE who had experienced AIS. Data were analyzed to determine age of onset, presenting signs and symptoms, and clinical features among this cohort compared with PHACE without AIS., Results: Twenty-two individuals with PHACE and AIS were identified. Imaging of the arteries of the head and neck was reported in 20 of 22. Narrowing or nonvisualization of at least 1 great cerebral vessel was present in 19 of 20 and of those, 15 had ≥ 2 vessels involved. Aortic arch anomalies were reported in 13 of 22 individuals., Conclusions: Aplasia, hypoplasia, or occlusion of a major cerebral artery appears to be a significant risk factor for AIS in children with PHACE, especially when >1 vessel is involved or if there is coarctation of the aorta.
- Published
- 2012
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47. Agminated, eruptive pyogenic granuloma-like lesions developing over congenital vascular stains.
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Baselga E, Wassef M, Lopez S, Hoffman W, Cordisco M, and Frieden IJ
- Subjects
- Female, Granuloma, Pyogenic congenital, Granuloma, Pyogenic pathology, Granuloma, Pyogenic surgery, Humans, Infant, Male, Treatment Outcome, Vascular Malformations pathology, Vascular Malformations surgery, Granuloma, Pyogenic diagnosis, Vascular Malformations diagnosis
- Abstract
We report three infants who developed agminated pyogenic granulomas over congenital vascular malformations, all of which had an aggressive growth pattern. There were no precipitating events such as laser therapy or surgery. Lesions were excised., (© 2011 Wiley Periodicals, Inc.)
- Published
- 2012
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48. Use of an extracorporeal membrane oxygenation circuit as a bridge to salvage a major upper-extremity replant in a critically ill patient.
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Greaney PJ Jr, Cordisco M, Rodriguez D, Newberger J, Legatt AD, and Garfein ES
- Subjects
- Accidents, Traffic, Critical Illness, Female, Follow-Up Studies, Heart Arrest therapy, Humans, Microsurgery methods, Multiple Trauma diagnosis, Multiple Trauma diagnostic imaging, Oxygen Consumption physiology, Postoperative Complications diagnosis, Postoperative Complications therapy, Regional Blood Flow, Replantation adverse effects, Risk Assessment, Treatment Outcome, Ultrasonography, Young Adult, Amputation, Traumatic surgery, Arm blood supply, Arm Injuries surgery, Replantation methods, Salvage Therapy methods
- Abstract
Major replantation of the upper extremity is defined as replantation at or above the level of the wrist. Selection of appropriate candidates is complex and requires consideration of many patient- and injury-associated factors including patient age, associated injuries, patient desire, mechanism of injury, ischemia time, wound condition, and presence of multiple-level injury. With respect to age, younger patients, especially children, are deemed to have a distinct advantage over more elderly patients due to improved nerve regeneration, and many advocate making every effort to replant this population. The risks of major upper-extremity replantation are significant and include bleeding, depletion of coagulation factors, secondary infection, and sepsis. As a result, major systemic illness and significant associated injuries are accepted as contraindications to limb salvage in this patient population. Herein we describe the use of an extracorporeal membrane oxygenation (ECMO) circuit as a potential bridge for short-term preservation of the extremity in a young patient with an acute, concomitant systemic illness. In the authors' opinion, use of ECMO perfusion is a viable means of maintaining extremity perfusion over hours or even days and may lead to broadened replant criteria in patients with associated injuries., (© Thieme Medical Publishers.)
- Published
- 2010
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49. Diagnosis of inadvertent cannulation of the azygos vein during cardiopulmonary bypass.
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Cordisco M, Newberger J, Shann KG, and Mellas NB
- Subjects
- Adult, Humans, Male, Vena Cava, Superior, Azygos Vein, Cardiopulmonary Bypass, Catheterization adverse effects, Medical Errors
- Abstract
Cardiac surgery with cardiopulmonary bypass demands diligence and attention to detail to prevent neurologic injury. Arterial and venous cannulae are used to facilitate cardiopulmonary bypass. The assessment of adequate decompression of the venous circulation is an essential duty of the cardiac surgical team. Modalities for the assessment of adequate regional venous drainage are limited, however communication between the team and increased awareness of certain pathologic states can be useful. These modalities include cerebral oximetry and superior vena caval pressure monitoring, which were employed during a case with bicaval venous cannulation. Malposition of the superior vena cava cannula was detected after a series of events alerted the team that superior vena cava drainage may be compromised.
- Published
- 2010
50. A novel association between RASA1 mutations and spinal arteriovenous anomalies.
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Thiex R, Mulliken JB, Revencu N, Boon LM, Burrows PE, Cordisco M, Dwight Y, Smith ER, Vikkula M, and Orbach DB
- Subjects
- Adult, Angiography, Arteriovenous Malformations diagnosis, Arteriovenous Malformations therapy, Child, Child, Preschool, Combined Modality Therapy, Embolization, Therapeutic, Female, Follow-Up Studies, Genotype, Hemangioma, Capillary diagnosis, Hemangioma, Capillary genetics, Hemangioma, Capillary therapy, Humans, Infant, Magnetic Resonance Imaging, Male, Microsurgery, Neoplasms, Multiple Primary diagnosis, Neoplasms, Multiple Primary genetics, Neoplasms, Multiple Primary therapy, Neurologic Examination, Postoperative Complications diagnosis, Skin Neoplasms diagnosis, Skin Neoplasms genetics, Skin Neoplasms therapy, Spinal Cord Compression diagnosis, Spinal Cord Compression genetics, Spinal Cord Compression therapy, Young Adult, Arteriovenous Malformations genetics, Chromosome Aberrations, DNA Mutational Analysis, Genes, Dominant genetics, Spinal Cord blood supply, p120 GTPase Activating Protein genetics
- Abstract
Background and Purpose: CM-AVM is a recently recognized autosomal dominant disorder associated with mutations in RASA1. Arteriovenous lesions have been reported in the brain, limbs, and the face in 18.5% of patients. We report a novel association between RASA1 mutations and spinal arteriovenous anomalies., Materials and Methods: In a collaborative study, 5 index patients (2 females, 3 males) with spinal AVMs or AVFs and cutaneous multifocal capillary lesions were investigated for the RASA1 gene mutation., Results: All 5 patients were found to have RASA1 mutation (2 de novo, 3 familial), and all had multifocal capillary malformations at birth. Neurologic deficits developed at ages ranging from infancy to early adulthood. All spinal anomalies (2 AVMs at the conus, 1 AVM at the lumbosacral junction, and 1 cervical and 1 cervicothoracic AVF) were complex, extensive, and fast-flow lesions. All patients required treatment based on the clinical and/or radiologic appearance of the lesions., Conclusions: To our knowledge, an association of RASA1 mutation and spinal AVM/AVF has not been described. MR imaging screening of patients with characteristic CMs and neurologic symptoms presenting at a young age may be useful in detecting the presence of fast-flow intracranial or intraspinal arteriovenous anomalies before potentially significant neurologic insult has occurred.
- Published
- 2010
- Full Text
- View/download PDF
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