27 results on '"Santecchia L"'
Search Results
2. The relationship between deficit in digit span and genotype in nonsense mutation Duchenne muscular dystrophy
- Author
-
Thangarajh, M, Elfring, GL, Trifillis, P, McIntosh, J, Peitz, SW, Ryan, MM, Kornberg, AJ, RodriguezCasero, V, Wray, A, Jones, KJ, North, K, Goemans, N, Buyse, GM, Campbell, C, Mah, J, Sarnat, H, Selby, K, Voit, T, Doppler, V, De Castro, D, Chabrol, B, Levy, N, Halbert, C, Pereon, Y, Magot, A, Perrier, J, Mahe, JY, Schara, U, Lutz, S, Busse, M, Della Marina, A, Kirschner, J, Stanescu, A, Pohl, A, RensingZimmerman, C, Bertini, E, D'Amico, A, Kofler, A, Carlesi, A, Bonetti, AM, Santecchia, L, Emma, F, Bergami, G, Mercuri, EM, Vasco, G, Bianco, F, Mazzone, ES, De Sanctis, R, Alfieri, P, Pane, M, Messina, S, Comi, GP, Magri, F, Lucchini, V, Corti, SP, Moggio, MG, Sciacco, M, Bresolin, N, Prelle, AC, Magri, R, Virgilio, R, Lamperti, C, Nevo, Y, DorWollman, T, Vilchez, J, Muelas, N, Sevilla, T, Smeyers, P, de la Osa, A, Colomer, J, Ortez, CI, Nascimento, A, Febrer, A, Medina, J, Tulinus, M, Thorarinsdottir, B, Darin, N, Sejersen, T, Hovmoller, M, Bushby, K, Straub, V, Guglieri, M, Sarkozy, A, Willis, T, Eagle, M, Mayhew, A, Muntoni, F, Cirak, S, Manzur, AY, Robb, SA, Kinali, M, Quinlivan, RCM, Smith, MR, Pandey, R, Wong, B, Collins, J, Finkel, R, Bonnemann, C, Yang, M, Foley, AR, Yum, S, Sampson, J, Bromberg, M, Swoboda, K, Day, J, Karachunski, P, Mathews, K, Bonthius, D, Laubenthal, KS, Darras, B, Kang, P, Parson, J, Barohn, R, Dasouki, M, Anderson, H, Burns, J, Dimachkie, M, Pasnoor, M, Wang, YX, Ciafaloni, E, Heatwole, C, Connolly, A, Pestronk, A, Al-Lozi, M, Lopate, G, Golumbek, P, Sommerville, B, Wang, L, Wojcicka-Mitchell, A, Godbey, A, Harms, M, Varadachary, A, Iyadurai, S, Rojas, L, Iannacone, S, Khonghatithum, C, Sproule, D, De Vivo, D, Constantinescu, A, McDonald, C, Han, J, Ben Renfroe, Russman, B, Sussman, M, BurnsWechsler, S, Juel, V, Hobson-Webb, L, Smith, E, Ataluren Phase 2b Study Grp, Schara, Ulrike (Beitragende*r), and Marina, Adela Della (Beitragende*r)
- Subjects
Male ,0301 basic medicine ,Adolescent ,Duchenne muscular dystrophy ,Nonsense mutation ,Medizin ,Neuropsychological Tests ,030105 genetics & heredity ,Article ,Young Adult ,03 medical and health sciences ,Exon ,Settore MED/39 - NEUROPSICHIATRIA INFANTILE ,0302 clinical medicine ,Genotype ,Memory span ,medicine ,Humans ,Child ,Genetics ,biology ,Promoter ,Duchenne ,medicine.disease ,Muscular Dystrophy, Duchenne ,Cross-Sectional Studies ,Memory, Short-Term ,Codon, Nonsense ,Child, Preschool ,Mutation (genetic algorithm) ,biology.protein ,Neurology (clinical) ,Dystrophin ,030217 neurology & neurosurgery - Abstract
ObjectiveTo evaluate the relationship between deficit in digit span and genotype in nonsense mutation (nm) Duchenne muscular dystrophy (DMD) (nmDMD).MethodsWe investigated the relationship between normalized digit-span forward (d-sf) and digit-span backward (d-sb) scores to the location of nmDMD mutations in 169 participants ≥5 to ≤20 years who participated in a phase 2b clinical trial. Because alternative promoters are found upstream of DMD exons 30, 45, and 63, we correlated d-sf and d-sb to the specific nmDMD mutation location.ResultsParticipants with nm downstream of exon 30, downstream of exon 45, and downstream of exon 63 had significantly lower normalized d-sf scores (p < 0.0001). Participants with nm downstream of exon 45 in addition had significantly lower normalized d-sb score (p < 0.04). There was no significant difference in the normalized d-sb score in participants with mutations upstream or downstream of DMD exon 30 or upstream or downstream of DMD exon 63.ConclusionOur data provide evidence that specific cognitive deficits correlate to genotype in individuals with nmDMD, highlighting the critical role of brain-specific dystrophin isoforms in the neurobiological manifestations of this disease.Clinicaltrials.gov identifierNCT02090959.
- Published
- 2018
- Full Text
- View/download PDF
3. Surgical management of congenital nevi: W5–3
- Author
-
De Stefano, C. and Santecchia, L.
- Published
- 1998
4. LOP37
- Author
-
Santecchia, L., primary
- Published
- 2015
- Full Text
- View/download PDF
5. O.346 Signiflcant craniofacial cleft in amniotic band syndrome
- Author
-
Latorre, S., primary, Zama, M., additional, Spuntarelli, G., additional, Santecchia, L., additional, Maggiulli, F., additional, and De Stefano, C., additional
- Published
- 2008
- Full Text
- View/download PDF
6. O.522 Head and neck vascular lesion in children
- Author
-
Urbani, U., primary, Santecchia, L., additional, Zama, M., additional, Spuntarelli, G., additional, and De Stefano, C., additional
- Published
- 2008
- Full Text
- View/download PDF
7. O.080 Secondary treatment of CLP patients: the facial skeleton
- Author
-
Santecchia, L., primary, Zama, M., additional, Spuntarelli, G., additional, Latorre, S., additional, and Maggiulli, F., additional
- Published
- 2008
- Full Text
- View/download PDF
8. O.081 Secondary treatment of CLP patients: the soft tissues
- Author
-
Zama, M., primary, Latorre, S., additional, Spuntarelli, G., additional, Santecchia, L., additional, and Maggiulli, F., additional
- Published
- 2008
- Full Text
- View/download PDF
9. O.497 Neoplasm of craniofacial skeleton in childhood
- Author
-
Maggiulli, F., primary, Spuntarelli, G., additional, Latorre, S., additional, Santecchia, L., additional, and Zama, M., additional
- Published
- 2008
- Full Text
- View/download PDF
10. O.181 Facial growth in CLP patients treated by periostioplasty
- Author
-
Spuntarelli, G., primary, Maggiulli, F., additional, Santecchia, L., additional, Latorre, S., additional, and Zama, M., additional
- Published
- 2008
- Full Text
- View/download PDF
11. Malignant tumors of the orbital region. Analysis of cases examined from 1986 to 1995
- Author
-
Seccia, Antonio, Salgarello, Marzia, Bracaglia, Roberto, Sturla, Marcella, Santecchia, L, Loreti, A, Farallo, Eugenio Giuseppe, Salgarello, Marzia (ORCID:0000-0003-4296-4214), Sturla, Marcella (ORCID:0000-0003-0288-3460), Seccia, Antonio, Salgarello, Marzia, Bracaglia, Roberto, Sturla, Marcella, Santecchia, L, Loreti, A, Farallo, Eugenio Giuseppe, Salgarello, Marzia (ORCID:0000-0003-4296-4214), and Sturla, Marcella (ORCID:0000-0003-0288-3460)
- Abstract
To present a retrospective study of 154 orbital tumors examined from 1986 to 1995.
- Published
- 1997
12. LOP37: Surgery for Lip Haemangiomas: A New Score of Severity, to Predict Functional and Cosmetic Results, according to the Aesthetic Units of the Face.
- Author
-
Santecchia, L.
- Published
- 2015
- Full Text
- View/download PDF
13. Vascular Anomalies Guidelines by the Italian Society for the study of Vascular Anomalies (SISAV)
- Author
-
F, Stillo, V, Baraldini, P, Dalmonte, M, El Hachem, R, Mattassi, G, Vercellio, B, Amato, C, Bellini, M, Bergui, G, Bianchini, A, Diociaiuti, C, Campisi, C, Gandolfo, C, Gelmetti, L, Moneghini, L, Monti, C, Magri, I, Neri, G, Paoloantonio, A, Patrizi, M, Rollo, L, Santecchia, M, Vaghi, N, Vercellino, Stillo, F, Baraldini, V, Dalmonte, P, El Hachem, M, Mattassi, R, Vercellio, G, Amato, B, Bellini, C, Bergui, M, Bianchini, G, Diociaiuti, A, Campisi, C, Gandolfo, C, Gelmetti, C, Moneghini, L, Monti, L, Magri, C, Neri, I, Paoloantonio, G, Patrizi, A, Rollo, M, Santecchia, L, Vaghi, M, Vercellino, N, and Vercellino, N.
- Subjects
Italy ,Vascular Malformations ,Humans ,Societies, Medical ,Human - Abstract
na
- Published
- 2015
14. The Use of ABILHAND-Kids in Children with Unilateral Congenital Below-Elbow Deficiencies and Acquired Amputation: An Italian Cross-Sectional Study.
- Author
-
Della Bella G, Santecchia L, Luttazi P, Mariani G, Pochiero L, Lacopo A, Delia C, and Tofani M
- Abstract
Congenital or acquired hand differences, including unilateral below-elbow deficiencies, present complex challenges in pediatric rehabilitation. Surgical management and prosthetic provision represent a big challenge to find a good balance for guaranteeing optimal hand function. There is no specific assessment tool for measuring these aspects in the Italian context. The present study investigates the psychometric properties of the ABILHAND-Kids in children with congenital unilateral below-elbow deficiencies and acquired amputation of the upper limb. We measure internal consistency using Cronbach coefficient alpha and the intraclass correlation coefficient (ICC) for measuring test-retest reliability. Differences in hand function in both children with acquired or congenital diseases were also investigated. Participants to the study were 107 (49 F and 58 M) children, with a mean (SD) age of 8.88 (4.25). For test retest reliability, conducted on a sub-sample of 58 children, the ICC was 0.92, while for internal consistency, the Cronbach coefficient alpha was 0.90. We did not find statistically significant differences in scoring ( p = 0.33) in the use (mean 29.25 SD 6.58) or non-use of a prosthetic device (mean 30.74 SD 7.43), while statistically significant differences were found in hand function ( p < 0.01) for children who had a congenital impairment (mean 31.87 SD 6.49) and children who had an acquired amputation (mean 27.77 SD 6.60). In conclusion, the ABILHAND-Kids showed good internal consistency and reliability and can capture differences in hand function in children with both congenital and acquired hand disorders.
- Published
- 2024
- Full Text
- View/download PDF
15. Effects of Mirror Neurons-Based Rehabilitation Techniques in Hand Injuries: A Systematic Review and Meta-Analysis.
- Author
-
Tofani M, Santecchia L, Conte A, Berardi A, Galeoto G, Sogos C, Petrarca M, Panuccio F, and Castelli E
- Subjects
- Humans, Mirror Neurons, Physical Therapy Modalities, Recovery of Function, Hand Injuries rehabilitation, Neurological Rehabilitation
- Abstract
Background: Hand trauma requires specific rehabilitation protocol depending on the different structures involved. According to type of surgical intervention, and for monitoring pain and edema, post-operative rehabilitation of a hand that has experienced trauma involves different timings for immobilization. Several protocols have been used to reduce immobilization time, and various techniques and methods are adopted, depending on the structures involved. Objective: To measure the effects of mirror neurons-based rehabilitation techniques in hand injuries throughout a systematic review and meta-analysis. Methods: The protocol was accepted in PROSPERO database. A literature search was conducted in Cinahl, Scopus, Medline, PEDro, OTseeker. Two authors independently identified eligible studies, based on predefined inclusion criteria, and extracted the data. RCT quality was assessed using the JADAD scale. Results: Seventy-nine suitable studies were screened, and only eleven were included for qualitative synthesis, while four studies were selected for quantitative analysis. Four studies were case reports/series, and seven were RCTs. Nine investigate the effect of Mirror Therapy and two the effect of Motor Imagery. Quantitative analyses revealed Mirror Therapy as effective for hand function recovery (mean difference = −14.80 95% Confidence Interval (CI) = −17.22, −12.38) (p < 0.00001) in the short term, as well as in long follow-up groups (mean difference = −13.11 95% Confidence Interval (CI) = −17.53, −8.69) (p < 0.00001). Clinical, but not statistical, efficacy was found for manual dexterity (p = 0.15), while no benefit was reported for range of motion. Conclusions: Mirror neurons-based rehabilitation techniques, combined with conventional occupational and physical therapy, can be a useful approach in hand trauma. Mirror therapy seems to be effective for hand function recovery, but, for motor imagery and action observation, there is not sufficient evidence to recommend its use. Further research on the efficacy of the mirror neurons-based technique in hand injury is recommended.
- Published
- 2022
- Full Text
- View/download PDF
16. Role of the Cadaver Lab in Lymphatic Microsurgery Education: Validation of a New Training Model.
- Author
-
Jiga LP, Campisi CC, Jandali Z, Ryan M, Maruccia M, Santecchia L, Cherubino M, and Georgiadis J
- Subjects
- Anastomosis, Surgical methods, Cadaver, Humans, Lymph Nodes surgery, Microsurgery methods, Lymphatic Vessels pathology, Lymphatic Vessels surgery, Lymphedema pathology, Lymphedema surgery
- Abstract
Background: Microsurgical transplantation of vascularized lymph nodes (VLNT) or lymphatic vessels (VLVT) alongside derivative lymphaticovenous procedures are promising approaches for treatment of lymphedema. However, clinically relevant training models for mastering these techniques are still lacking. Here we describe a new training model in human cadaver and validate its use as training tool for microsurgical lymphatic reconstruction., Methods: 10 surgeons with previous exposure to microsurgery were trained in a controlled environment. Lymphatic vessel mapping and dissection in 4 relevant body regions, harvesting of five different VLNTs and one VLVT were performed in 5 fresh-frozen cadavers. The number of lymphatic vessels and lymph nodes for each VLNT were recorded. Finally, the efficacy of this model as training tool was validated using the Dundee Ready Education Environment Measure (DREEM)., Results: The average cumulative DREEM score over each category was 30,75 (max = 40) while individual scoring for each relevant category revealed highly positive ratings from the perspective of teaching (39,3), training 40,5 (max = 48) and self perception of the training 30,5 (max = 32) from all participants. The groin revealed the highest number of lymphatic vessels (3.2 ± 0.29 ) as all other regions on the upper extremity, while the gastroepiploic VLNT had the highest number of lymph nodes (4.2 ± 0.37)., Conclusions: This human cadaver model represents a new, reproducible "all-in-one" tool for effective training in lymphatic microsurgery. Its unique diligence in accurately reproducing human lymphatic anatomy, should make this model worth considering for each microsurgeon willing to approach lymphatic reconstruction.
- Published
- 2022
- Full Text
- View/download PDF
17. Guidelines for Vascular Anomalies by the Italian Society for the study of Vascular Anomalies (SISAV).
- Author
-
Stillo F, Mattassi R, Diociaiuti A, Neri I, Baraldini V, Dalmonte P, Amato B, Ametrano O, Amico G, Bianchini G, Campisi C, Cattaneo E, Causin F, Cavalli R, Colletti G, Corbeddu M, Coppo P, DE Fiores A, DI Giuseppe P, El Hachem M, Esposito F, Fulcheri E, Gandolfo C, Grussu F, Guglielmo A, Leuzzi M, Manunza F, Moneghini L, Monzani N, Nicodemi E, Occella C, Orso M, Pagella F, Paolantonio G, Pasetti F, Rollo M, Ruggiero F, Santecchia L, Spaccini L, Taurino M, Vaghi M, Vercellio G, Zama M, Zocca A, Aguglia M, Castronovo EL, DE Lorenzi E, Fontana E, Gusson E, Lanza J, Lizzio R, Mancardi MM, and Rosina E
- Subjects
- Humans, Italy, Vascular Diseases, Vascular Malformations diagnosis, Vascular Malformations therapy
- Published
- 2022
- Full Text
- View/download PDF
18. An Italian Validation of ABILHAND-Kids for Children With Cerebral Palsy.
- Author
-
Tofani M, Blasetti G, Lucibello L, Berardi A, Galeoto G, Sabbadini M, Santecchia L, and Castelli E
- Subjects
- Child, Disability Evaluation, Hand, Humans, Reproducibility of Results, Surveys and Questionnaires, Cerebral Palsy
- Abstract
Limitations in hand function are common among children with cerebral palsy (CP), with almost 50% presenting an arm-hand dysfunction. However, there is no standardized assessment tool available in Italian for evaluating bimanual performance for this population. Our objective in this study was to evaluate the psychometric properties of an Italian translation of the ABILHAND-Kids (ABILHAND-Kids-IT) among children with CP. We examined internal consistency using Cronbach's Alpha and Omega coefficients, and we investigated test-retest reliability with intraclass correlation coefficients (ICC). We performed explorative factor analysis (EFA) to investigate structural validity. We calculated Pearson's correlation coefficients between the ABILAND-Kids IT and the Manual Ability Classification System (MACS) to assess criterion validity; and, to demonstrate the score variability of the ABILHAND-Kids-IT, we used analyses of variance (ANOVAs) to compare the 181 children with CP in this sample with their levels on the MACS. We enrolled 181 children with CP in the study. EFA confirmed a uni-dimensional scale. We obtained internal consistency on both Cronbach's Alpha and Omega coefficient of 0.98, and a one-week test-retest reliability analysis revealed an ICC with 95% of confidence interval of .992. The ANOVA revealed significant score variability ( p < 0.01) and the Pearson correlation coefficient comparing the ABILHAND-Kids-It score with the MACS was -0.929 ( p < 0.01). We conclude that the ABILHAND-Kids-IT is valid and reliable for use with Italian children with CP.
- Published
- 2021
- Full Text
- View/download PDF
19. Hand and Upper Limb Malformations in Italy: A Multicentric Study.
- Author
-
Senes FM, Calevo MG, Adani R, Baldrighi C, Bassetto F, Corain M, Landi A, Lando M, Monticelli A, Novelli C, Pajardi G, Rosanda E, Rossello MI, Santecchia L, Zoccolan A, and Catena N
- Subjects
- Child, Female, Humans, Infant, Italy epidemiology, Male, Retrospective Studies, Hand surgery, Hand Deformities, Upper Extremity
- Abstract
Background: Although hand and upper limb malformations are quite frequent, up to now very few reports have been published on epidemiology. The aim of this study is to evaluate the number of infants who presented with hand and upper limb malformations from 2010 to 2015 in Italy. Methods: A retrospective analysis of a pediatric population presenting with hand and upper extremity malformations was carried out, gathering reports achieved from eight Italian Centers of pediatric hand surgery. Other factors such as gender, date and region of birth, family distribution of malformations and associated syndromes, were analysed. Results: Out of 3,100,421 live births, 765 children presented with hand and upper limb malformations. The incidence was 2,5/10,000 live births with a predominance of males and the right side. Radial polydactyly was the anomaly with the highest percentage, closely followed by simple syndactyly, simbrachidactyly and complex syndactyly. Less common conditions were the triphalangic thumb, thumb in palm, proximal radioulnar synostosis and Sprengel deformity. Inheritance of and familial predisposition to those malformations was recorded in 25 cases, while 84 children presented with syndromes related to hand anomalies. Conclusions: In conclusion the incidence of hand and upper extremity malformations in Italy is lower than that registered in other countries. The retrospective nature of the study combined with the fact that some defects frequently evade pediatric hand surgeon consultations are some possible limitations of the study. However, our data confirmed that, in spite of the decrease in the birth rate in Italy, the trend of congenital hand disorders maintained a stable trend. We aim to integrate this study with a prospective analysis and to involve the institutional health authorities in other countries so as to register the correct incidence of hand and upper extremity defects.
- Published
- 2021
- Full Text
- View/download PDF
20. The Versatility of the Free Vastus Lateralis Muscle Flap: Orbital Reconstruction After Removal of Complex Vascular Malformation in a Pediatric Patient.
- Author
-
Grussu F, Santecchia L, Urbani U, Spuntarelli G, Rollo M, El Hachem M, Romanzo A, and Zama M
- Abstract
Introduction: Vascular orbital lesions in pediatric population represent a demanding therapeutic challenge which requires a multidisciplinary team. In severe cases, orbital enucleation can be considered. Surgical management of enucleated orbital region in children, differently from the adults, represents a challenging procedure owing to the intrinsic relation between volume replacement and normal orbital growth. Many reconstructive options have been proposed, and many donor sites have been utilized for this purpose but each one have demonstrated potential disadvantages. Despite its well-known versatility, no report of the vastus lateralis free flap in children requiring orbital reconstruction exists in literature. Herein, we propose this surgical strategy as a valid option for the reconstruction of an extended orbital defect in a pediatric patient suffering from a mixed type of vascular malformation. Material and Methods: A patient was referred from a foreign country with an unclear medical history, presenting exorbitism and exophthalmos, proptosis of the eyeball, visus 4/10, and limited ocular motility. We made clinical-instrumental investigations with a diagnosis of complex vascular malformation. It expanded in intraorbital and retrorbital space with bulb anterior dislocation and optic nerve involvement. We performed an emptying of the orbital content via transconjunctival and via coronal incision with eyelid preservation. A free vastus lateralis muscle flap was used for reconstruction, filling the orbital cavity. We anastomosed the flap on the superficial temporal artery. An ocular conformator was then positioned. Results: We report the result at 12 months, showing a good orbital rehabilitation with an adequate prosthetic cavity, a good recovery of volume and facial symmetry, guaranteeing balanced orbital and periorbital growth. There were no major or minor complications associated with the procedure. Discussion: The reconstruction of the orbit remains a "surgical challenge" both in adults, whose goal is the restoration of volume, adequate symmetry and facial esthetics, and children, in which correcting the asymmetry has the additional objective to balance orbital growth. Many reconstructive techniques have been proposed, including the use of free flaps. The versatility of the free vastus lateralis muscle flap is well-known. It offers adequate amount of tissue with minimal morbidity to the donor site, provides a long pedicle, gives the possibility of simultaneous work in a double team, and has a constant anatomy and a safe and rapid dissection. There are no descriptions of its use for pediatric orbital reconstructions. Conclusions: In our opinion, the free vastus lateralis flap should be included as one of the best option for orbital pediatric reconstruction after enucleation., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2021 Grussu, Santecchia, Urbani, Spuntarelli, Rollo, El Hachem, Romanzo and Zama.)
- Published
- 2021
- Full Text
- View/download PDF
21. Interosseous Membrane Release for Long-Standing Upper Limb Lymphedema: A Procedure Often Neglected.
- Author
-
Santecchia L, Ciudad P, Mouchammed A, Amoroso M, and Chen HC
- Published
- 2017
- Full Text
- View/download PDF
22. Vascular Anomalies Guidelines by the Italian Society for the study of Vascular Anomalies (SISAV).
- Author
-
Stillo F, Baraldini V, Dalmonte P, El Hachem M, Mattassi R, Vercellio G, Amato B, Bellini C, Bergui M, Bianchini G, Diociaiuti A, Campisi C, Gandolfo C, Gelmetti C, Moneghini L, Monti L, Magri C, Neri I, Paoloantonio G, Patrizi A, Rollo M, Santecchia L, Vaghi M, and Vercellino N
- Subjects
- Humans, Italy, Vascular Malformations epidemiology, Vascular Malformations etiology, Societies, Medical standards, Vascular Malformations classification, Vascular Malformations diagnosis, Vascular Malformations therapy
- Published
- 2015
23. Early surgical excision of giant congenital hemangiomas of the scalp in newborns: clinical indications and reconstructive aspects.
- Author
-
Santecchia L, Francesca Bianciardi Valassina M, Maggiulli F, Spuntarelli G, De Vito R, and Zama M
- Subjects
- Female, Head and Neck Neoplasms congenital, Hemangioma, Capillary congenital, Humans, Infant, Neoplastic Syndromes, Hereditary congenital, Skin Neoplasms congenital, Head and Neck Neoplasms surgery, Hemangioma, Capillary surgery, Neoplastic Syndromes, Hereditary surgery, Scalp surgery, Skin Neoplasms surgery
- Abstract
Background: Infantile hemangioma is the most common vascular tumor in newborns, with an incidence from 12 to 23% among preterm infants with low weight at birth and a female to male ratio of 3:1. The head and neck is the most frequently affected area (60%), and the scalp is a typical site for such large lesions., Objective: We describe some clinical and medical aspects in comparison with the surgical approach to giant infantile hemangioma of the scalp., Methods: The indications to treatment are discussed. An outcome basis evaluation, by reviewing some clinical cases, is provided to help readers better understand when and how to undergo surgery safely., Conclusion: Early excision of huge infantile hemangioma of the scalp is the treatment of choice if feasible within 5 months of age.
- Published
- 2013
- Full Text
- View/download PDF
24. Minor salivary gland neoplasm in children.
- Author
-
Spuntarelli G, Santecchia L, Urbani U, and Zama M
- Subjects
- Adolescent, Child, Diagnosis, Differential, Diagnostic Imaging, Female, Humans, Salivary Gland Neoplasms pathology, Surgical Flaps, Salivary Gland Neoplasms diagnosis, Salivary Gland Neoplasms surgery, Salivary Glands, Minor pathology
- Abstract
In this article, we present a review of the literature, and we focus on 2 particular cases of cancer of the salivary glands accessory in pediatric patients The accessory parotid is the site of congenital and acquired lesions. In adults, the acquired lesions are often neoplastic and are usually similar to those seen in the main parotid gland. The disorders in children are less well defined, as only a few cases have been reported.The accessory parotid gland, or accessory parotid, is a nodule of normal salivary tissue separated from the main parotid gland, located on the masseter muscle, to which it is bound by an extension of the masseteric fascia and connected to the Stensen duct at that level. In contrast to the extensive literature on acquired lesions of the accessory parotid in adults, very few cases of malignant or benign lesions of the accessory parotid in children could be found in the literature. A review of several articles reporting lesions of the accessory parotid in adult patients, reporting 3 or more cases each for a total of 71 patients, showed 24 malignant neoplasms, 39 benign neoplasms, and 8 nonneoplastic lesions. Lesions of the accessory parotid are quite rare in children but should be considered when facing mass located in the cheek.
- Published
- 2013
- Full Text
- View/download PDF
25. Early reconstruction of the abdominal wall in giant omphalocele.
- Author
-
Zama M, Gallo S, Santecchia L, Bertozzi E, Zaccara A, Trucchi A, Nahom A, Bagolan P, and De Stefano C
- Subjects
- Female, Humans, Infant, Newborn, Male, Surgical Flaps, Surgical Mesh, Treatment Outcome, Abdominal Wall surgery, Hernia, Umbilical surgery, Plastic Surgery Procedures methods
- Abstract
Omphalocele is the most common congenital defect of the abdominal wall. Mortality rate is between 20 and 70% and early closure of the abdominal wall, within 10 days of life, is vital to the successful outcome of the surgical treatment. The authors describe the use of two bipedicled flaps of abdominal skin to correct the defect of the midline as soon as the reduction of all viscera has been accomplished.
- Published
- 2004
- Full Text
- View/download PDF
26. Juvenile active ossifying fibroma with massive involvement of the mandible.
- Author
-
Zama M, Gallo S, Santecchia L, Bertozzi E, and De Stefano C
- Subjects
- Child, Fibroma, Ossifying surgery, Humans, Male, Mandibular Neoplasms surgery, Fibroma, Ossifying diagnosis, Mandibular Neoplasms diagnosis
- Abstract
Fibro-osseous lesions of the maxillofacial complex are often difficult to diagnose from both a clinical and a histopathologic point of view. The parameters for the diagnosis of juvenile active ossifying fibroma are as follows: a patient under 15 years of age, localization of the tumor, the radiologic aspect, and the tendency to recur. Although many authors favor conservative surgery rather than radical en bloc resection, immediate recurrence characterized by a high aggressive growth rate and the absence of a distinct separation between the tumor and the adjacent bone requires ex- tensive surgery, with wide demolition of the involved bone.
- Published
- 2004
- Full Text
- View/download PDF
27. Malignant tumors of the orbital region. Analysis of cases examined from 1986 to 1995.
- Author
-
Seccia A, Salgarello M, Bracaglia R, Sturla M, Santecchia L, Loreti A, and Farallo E
- Subjects
- Carcinoma, Basal Cell pathology, Carcinoma, Squamous Cell pathology, Female, Humans, Male, Middle Aged, Orbital Neoplasms surgery, Retrospective Studies, Orbital Neoplasms pathology
- Abstract
Objective: To present a retrospective study of 154 orbital tumors examined from 1986 to 1995., Methods: We analyzed the clinical behavior and the degree of local malignity also in relationship with the particular anatomical characteristics of this site., Results: In this are, it is not rare finding tumors with a scarce cutaneous extension but a deep involvement including the bone, or of recurrences after a previous insufficient treatment with an aggressive clinical course., Conclusion: The principles for the surgical approach are: exeresis as radical as possible, one-stage operation for tumoral resection and reconstruction, bringing of trophic tissue able to sustain any complementary treatment, easy and fast execution, and short clinical course.
- Published
- 1997
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.