25 results on '"Roggero L."'
Search Results
2. Primary Sclerosing Cholangitis and Amyloid A Amyloidosis: Association or Coincidence?
- Author
-
Lacetera R., Roggero L., Vercelloni P., Uzzo M., Carbone M., Invernizzi P., L'Imperio V., Pieruzzi F., Sinico R. A., Lacetera, R, Roggero, L, Vercelloni, P, Uzzo, M, Carbone, M, Invernizzi, P, L'Imperio, V, Pieruzzi, F, and Sinico, R
- Subjects
Nephrology ,Nephrotic syndrome ,AA amyloidosi ,Primary sclerosing cholangiti - Abstract
AA amyloidosis may complicate several chronic inflammatory conditions. From a clinical point of view, causality between inflammatory pathology and AA amyloidosis can be assumed because of the data described in the literature; some of the best known include rheumatoid arthritis, ankylosing spondylitis, inflammatory bowel disease, and chronic infections. Singles cases of inflammatory diseases have been found at AA amyloidosis. Causality becomes more plausible if at least two different cases with AA amyloidosis are both found to have the same rare inflammatory disease. We describe the case of a patient with primary sclerosing cholangitis (PSC) with development of AA amyloidosis conditioning a nephrotic syndrome, likely secondary to failure to control the chronic inflammatory process. Only two cases in the literature describe the association of this rare disease and the appearance of AA amyloidosis. The treatment of AA amyloidosis consists in treating the underlying inflammatory disorder; to date, few effective treatments are available for PSC. Therefore, and in view of the limited data in the literature, we believe it is important to describe its association.
- Published
- 2022
3. Primary Sclerosing Cholangitis and Amyloid A Amyloidosis: Association or Coincidence?
- Author
-
Lacetera, R, Roggero, L, Vercelloni, P, Uzzo, M, Carbone, M, Invernizzi, P, L'Imperio, V, Pieruzzi, F, Sinico, R, Lacetera R., Roggero L., Vercelloni P., Uzzo M., Carbone M., Invernizzi P., L'Imperio V., Pieruzzi F., Sinico R. A., Lacetera, R, Roggero, L, Vercelloni, P, Uzzo, M, Carbone, M, Invernizzi, P, L'Imperio, V, Pieruzzi, F, Sinico, R, Lacetera R., Roggero L., Vercelloni P., Uzzo M., Carbone M., Invernizzi P., L'Imperio V., Pieruzzi F., and Sinico R. A.
- Abstract
AA amyloidosis may complicate several chronic inflammatory conditions. From a clinical point of view, causality between inflammatory pathology and AA amyloidosis can be assumed because of the data described in the literature; some of the best known include rheumatoid arthritis, ankylosing spondylitis, inflammatory bowel disease, and chronic infections. Singles cases of inflammatory diseases have been found at AA amyloidosis. Causality becomes more plausible if at least two different cases with AA amyloidosis are both found to have the same rare inflammatory disease. We describe the case of a patient with primary sclerosing cholangitis (PSC) with development of AA amyloidosis conditioning a nephrotic syndrome, likely secondary to failure to control the chronic inflammatory process. Only two cases in the literature describe the association of this rare disease and the appearance of AA amyloidosis. The treatment of AA amyloidosis consists in treating the underlying inflammatory disorder; to date, few effective treatments are available for PSC. Therefore, and in view of the limited data in the literature, we believe it is important to describe its association.
- Published
- 2022
4. Relapsing minimal change disease superimposed on late-onset p.N215S Fabry nephropathy
- Author
-
Salerno, F, Roggero, L, Rossi, F, Binaggia, A, Bertoli, S, Pieruzzi, F, Salerno F. R., Roggero L., Rossi F., Binaggia A., Bertoli S., Pieruzzi F., Salerno, F, Roggero, L, Rossi, F, Binaggia, A, Bertoli, S, Pieruzzi, F, Salerno F. R., Roggero L., Rossi F., Binaggia A., Bertoli S., and Pieruzzi F.
- Abstract
We present the case of a 76-year-old man with late-onset Fabry disease caused by the p.N215S missense mutation, with Fabry cardiomyopathy and nephropathy. In this case, the diagnosis of Fabry disease was incidental and followed minimal change disease (MCD) onset, with nephrotic syndrome and acute kidney injury requiring renal replacement therapy. Fabry nephropathy associated with the p.N215S mutation is becoming increasingly recognized among older patients. The importance of electron microscopy is herein highlighted and histological features common to Fabry nephropathy and MCD are discussed, along with the challenges associated with the diagnosis and clinical management.
- Published
- 2022
5. Erratum: Erratum to: Relapsing Minimal Change Disease Superimposed on Late-Onset p.N215S Fabry Nephropathy (Clinical Kidney Journal (2022) 15:4 (839) DOI: 10.1093/ckj/sfab148)
- Author
-
Salerno F. R., Salerno, F, Roggero, L, Rossi, F, Binaggia, A, Bertoli, S, Pieruzzi, F, Salerno F. R., Roggero L., Rossi F., Binaggia A., Bertoli S., Pieruzzi F., Salerno F. R., Salerno, F, Roggero, L, Rossi, F, Binaggia, A, Bertoli, S, Pieruzzi, F, Salerno F. R., Roggero L., Rossi F., Binaggia A., Bertoli S., and Pieruzzi F.
- Published
- 2022
6. Long-term results of rectus fascial sling in women with severe stress urinary incontince: a high-volume single-center experience
- Author
-
Balzarro, M., primary, Rubilotta, E., additional, Ditonno, F., additional, Gentile, I., additional, Princiotta, A., additional, Bianchi, A., additional, Serafin, E., additional, Roggero, L., additional, Cerruto, M.A., additional, and Antonelli, A., additional
- Published
- 2022
- Full Text
- View/download PDF
7. Elevated Ambulatory Blood Pressure Measurements are Associated with a Progressive Form of Fabry Disease
- Author
-
Rossi, F, Svarstad, E, Elsaid, H, Binaggia, A, Roggero, L, Auricchio, S, Marti, H, Pieruzzi, F, Rossi F., Svarstad E., Elsaid H., Binaggia A., Roggero L., Auricchio S., Marti H. -P., Pieruzzi F., Rossi, F, Svarstad, E, Elsaid, H, Binaggia, A, Roggero, L, Auricchio, S, Marti, H, Pieruzzi, F, Rossi F., Svarstad E., Elsaid H., Binaggia A., Roggero L., Auricchio S., Marti H. -P., and Pieruzzi F.
- Abstract
Introduction: Published data on hypertension incidence and management in Anderson–Fabry disease are scant and the contribution of elevated blood pressure to organ damage is not well recognized. Aim: Therefore, we have assessed blood pressure values and their possible correlations with clinical findings in a well described cohort of Fabry patients. Methods: Between January 2015 and May 2019, all adult Fabry patients (n = 24 females, n = 8 males) referred to our institute were prospectively enrolled. During the first examination patient’s genotype and clinical characteristics were recorded. Blood pressure data were obtained by standard observed office measurements followed, within 6 months, by ambulatory blood pressure monitoring and home self-recordings. Organ involvement, including kidneys, heart and brain, was monitored over time. Consequently, patients were defined as clinically stable or progressive through the Fabry Stabilization Index. Results: The standard office measurements have diagnosed hypertension in three (9.37%) patients, but the ambulatory monitoring showed elevated blood pressure in six (18.75%) patients, revealing three cases of masked hypertension. All the hypertensive patients were females and, compared with normotensive subjects, they presented a lower glomerular filtration rate (p < 0.05) and a more advanced cardiac hypertrophy (p < 0.05). Four (66.7%) of them were diagnosed with a progressive form of the disease through the Fabry Stabilization Index while the majority of the normotensive group (84.6%, n = 19) was stable over time. No correlation was found between the prevalence of hypertension and the type of mutations causing Fabry disease. Conclusion: Hypertension can be found in a restricted portion of clinically stable Fabry patients. In contrast, patients presenting with a progressive organ involvement, particularly renal impairment, have a major risk of developing uncontrolled blood pressure, and should be followed carefully. Moreov
- Published
- 2021
8. SC262 - Long-term results of rectus fascial sling in women with severe stress urinary incontince: a high-volume single-center experience
- Author
-
Balzarro, M., Rubilotta, E., Ditonno, F., Gentile, I., Princiotta, A., Bianchi, A., Serafin, E., Roggero, L., Cerruto, M.A., and Antonelli, A.
- Published
- 2022
- Full Text
- View/download PDF
9. La terapia enzimatica sostitutiva nella malattia di Fabry
- Author
-
Roggero, L, Auricchio, S, Pieruzzi, F, Roggero, Letizia, Auricchio, Sara, Pieruzzi, Federico, Roggero, L, Auricchio, S, Pieruzzi, F, Roggero, Letizia, Auricchio, Sara, and Pieruzzi, Federico
- Abstract
Enzyme Replacement Therapy for Fabry Disease Anderson-Fabry disease (FD) is a X-linked lysosomal storage disorder, which involves glycosphingolipids metabolism. Specific treatment for FD has been available in the last two decades, after the development and commercialization of recombinant human alfa-galactosidase A. Since then enzyme replacement therapy (ERT) has changed the natural history of the disease. Two different enzymatic formulations are available: agalsidase alfa and agalsidase beta at different dosages. The safety and efficacy profiles are similar. ERT induces Gb3 deposits reduction in renal and cardiac biopsies, improves quality of life, reduces pain and GI symptoms, decreases left ventricular mass and slows down renal function decline. In case of organ involvement, clinical evidence confirms the need to treat all patients with enzyme therapy, both male and female. In all other clinical settings, the decision to start ERT is controversial, because of the extremely variable clinical manifestations of FD. However, data suggest a greater response to ERT if started as early as possible in any patients. Timely treatment appears to be effective in stabilizing and possibly delaying FD progression. ERT infusion reactions due to allergic hypersensitivity or IgG antibody development could occur but can be easily managed. In-hospital and at home infusions are possible. The wide genetic and phenotypic heterogeneity observed in all FD patients requires a tailored approach to treatment options. Patients should be referred to an expert multidisciplinary team for the long term management of this challenging disease.
- Published
- 2019
10. V119 - Nightmare surgical scenario during robotic nephroureterectomy for unexpected ureteral endometriosis infiltrating the external iliac artery.
- Author
-
Roggero, L., Brancelli, C., Corghi, G., Migliorini, F., Cerruto, M.A., Bertolo, R.G., Veccia, A., and Antonelli, A.
- Subjects
- *
ILIAC artery , *ENDOMETRIOSIS , *ROBOTICS - Published
- 2024
- Full Text
- View/download PDF
11. Denosumab or oral bisphosphonates in primary osteoporosis: a “real-life” study
- Author
-
Cairoli, E., primary, Palmieri, S., additional, Goggi, G., additional, Roggero, L., additional, Arosio, M., additional, Chiodini, I., additional, and Eller-Vainicher, C., additional
- Published
- 2018
- Full Text
- View/download PDF
12. Elevated Ambulatory Blood Pressure Measurements are Associated with a Progressive Form of Fabry Disease
- Author
-
Sara Auricchio, Letizia Roggero, Einar Svarstad, Agnese Binaggia, Hans-Peter Marti, Federico Pieruzzi, Hassan Elsaid, Federica Rossi, Rossi, F, Svarstad, E, Elsaid, H, Binaggia, A, Roggero, L, Auricchio, S, Marti, H, and Pieruzzi, F
- Subjects
Adult ,Male ,0301 basic medicine ,medicine.medical_specialty ,Ambulatory blood pressure ,Lysosomal storage disorder ,Renal function ,Blood Pressure ,Masked hypertension ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,Internal Medicine ,medicine ,Humans ,Aged ,Anderson–Fabry disease ,business.industry ,Incidence (epidemiology) ,Blood Pressure Monitoring, Ambulatory ,Middle Aged ,medicine.disease ,Fabry disease ,Blood pressure monitoring ,Masked Hypertension ,030104 developmental biology ,Blood pressure ,Hypertension ,Cohort ,Ambulatory ,Disease Progression ,Cardiology ,Fabry Disease ,Original Article ,Female ,Cardiology and Cardiovascular Medicine ,business ,030217 neurology & neurosurgery - Abstract
Introduction Published data on hypertension incidence and management in Anderson–Fabry disease are scant and the contribution of elevated blood pressure to organ damage is not well recognized. Aim Therefore, we have assessed blood pressure values and their possible correlations with clinical findings in a well described cohort of Fabry patients. Methods Between January 2015 and May 2019, all adult Fabry patients (n = 24 females, n = 8 males) referred to our institute were prospectively enrolled. During the first examination patient’s genotype and clinical characteristics were recorded. Blood pressure data were obtained by standard observed office measurements followed, within 6 months, by ambulatory blood pressure monitoring and home self-recordings. Organ involvement, including kidneys, heart and brain, was monitored over time. Consequently, patients were defined as clinically stable or progressive through the Fabry Stabilization Index. Results The standard office measurements have diagnosed hypertension in three (9.37%) patients, but the ambulatory monitoring showed elevated blood pressure in six (18.75%) patients, revealing three cases of masked hypertension. All the hypertensive patients were females and, compared with normotensive subjects, they presented a lower glomerular filtration rate (p < 0.05) and a more advanced cardiac hypertrophy (p < 0.05). Four (66.7%) of them were diagnosed with a progressive form of the disease through the Fabry Stabilization Index while the majority of the normotensive group (84.6%, n = 19) was stable over time. No correlation was found between the prevalence of hypertension and the type of mutations causing Fabry disease. Conclusion Hypertension can be found in a restricted portion of clinically stable Fabry patients. In contrast, patients presenting with a progressive organ involvement, particularly renal impairment, have a major risk of developing uncontrolled blood pressure, and should be followed carefully. Moreover, the ambulatory blood pressure monitoring proved to be useful to reveal masked hypertension, which can contribute to the progressive worsening of the organ damage. Therefore, a proper diagnosis and therapy of hypertension may improve the outcome of Fabry patients. Supplementary Information The online version contains supplementary material available at 10.1007/s40292-021-00450-0.
- Published
- 2021
13. Relapsing minimal change disease superimposed on late-onset p.N215S Fabry nephropathy
- Author
-
Fabio R Salerno, Silvio Bertoli, Federico Pieruzzi, Federica Rossi, Letizia Roggero, Agnese Binaggia, Salerno, F, Roggero, L, Rossi, F, Binaggia, A, Bertoli, S, and Pieruzzi, F
- Subjects
Fabry disease ,Genotype-phenotype correlation ,Transplantation ,medicine.medical_specialty ,business.industry ,Superimposed glomerulopathie ,superimposed glomerulopathies ,Nephrotic syndrome ,Late onset ,genotype–phenotype correlation ,medicine.disease ,Acute kidney injury ,Nephropathy ,Fabry nephropathy ,Nephrology ,Internal medicine ,Exceptional Case ,Cardiology ,medicine ,Minimal change disease ,AcademicSubjects/MED00340 ,business - Abstract
We present the case of a 76-year-old man with late-onset Fabry disease caused by the p.N215S missense mutation, with Fabry cardiomyopathy and nephropathy. In this case, the diagnosis of Fabry disease was incidental and followed minimal change disease (MCD) onset, with nephrotic syndrome and acute kidney injury requiring renal replacement therapy. Fabry nephropathy associated with the p.N215S mutation is becoming increasingly recognized among older patients. The importance of electron microscopy is herein highlighted and histological features common to Fabry nephropathy and MCD are discussed, along with the challenges associated with the diagnosis and clinical management.
- Published
- 2021
14. A0883 - Long-term results of women suffering from severe stress urinary incontince treated with rectus fascial sling: A high-volume single-center experience.
- Author
-
Balzarro, M., Rubilotta, E., Ditonno, F., Gentile, I., Princiotta, A., Bianchi, A., Serafin, E., Roggero, L., Cerruto, M.A., and Antonelli, A.
- Subjects
- *
URINARY stress incontinence , *SUFFERING - Published
- 2023
- Full Text
- View/download PDF
15. La terapia enzimatica sostitutiva nella malattia di Fabry
- Author
-
Sara Auricchio, Letizia Roggero, Federico Pieruzzi, Roggero, L, Auricchio, S, and Pieruzzi, F
- Subjects
0303 health sciences ,lcsh:Internal medicine ,Alpha-galactosidase ,biology ,business.industry ,030305 genetics & heredity ,Fabry disease, lysosomal storage disease, alpha-galactosidase, enzyme replacement therapy, algasidase ,General Medicine ,Enzyme replacement therapy ,medicine.disease ,lcsh:Diseases of the genitourinary system. Urology ,lcsh:RC870-923 ,Fabry disease ,Molecular biology ,03 medical and health sciences ,Lysosomal storage disease ,medicine ,biology.protein ,business ,lcsh:RC31-1245 ,030304 developmental biology - Abstract
Enzyme Replacement Therapy for Fabry Disease Anderson-Fabry disease (FD) is a X-linked lysosomal storage disorder, which involves glycosphingolipids metabolism. Specific treatment for FD has been available in the last two decades, after the development and commercialization of recombinant human alfa-galactosidase A. Since then enzyme replacement therapy (ERT) has changed the natural history of the disease. Two different enzymatic formulations are available: agalsidase alfa and agalsidase beta at different dosages. The safety and efficacy profiles are similar. ERT induces Gb3 deposits reduction in renal and cardiac biopsies, improves quality of life, reduces pain and GI symptoms, decreases left ventricular mass and slows down renal function decline. In case of organ involvement, clinical evidence confirms the need to treat all patients with enzyme therapy, both male and female. In all other clinical settings, the decision to start ERT is controversial, because of the extremely variable clinical manifestations of FD. However, data suggest a greater response to ERT if started as early as possible in any patients. Timely treatment appears to be effective in stabilizing and possibly delaying FD progression. ERT infusion reactions due to allergic hypersensitivity or IgG antibody development could occur but can be easily managed. In-hospital and at home infusions are possible. The wide genetic and phenotypic heterogeneity observed in all FD patients requires a tailored approach to treatment options. Patients should be referred to an expert multidisciplinary team for the long term management of this challenging disease.
- Published
- 2019
16. Tumor location at trans-urethral resection is predictive of ipsilateral pelvic lymph-nodal metastases in patients undergoing radical cystectomy for bladder cancer.
- Author
-
Cianflone F, Mazzucato G, Rubilotta E, Orlando R, De Maria N, Boldini M, Fumanelli F, Montanaro F, Pettenuzzo G, Roggero L, Gozzo A, Bianchi A, Veccia A, Bertolo RG, Cerruto MA, and Antonelli A
- Abstract
Objective: To assess whether tumor location at diagnostic TURBT is predictive of ipsilateral nodal involvement in patients who underwent radical cystectomy (RC) with lymph-nodes dissection for bladder cancer (BCa)., Materials and Methods: All patients who underwent RC for BCa at a single institution between 2014-2023 were assessed. Tumor location at TURBT was defined as right-sided, median-line, left-sided, and diffused. Distribution in the percentage of ipsilateral positive lymph-nodes and number of ipsilateral positive lymph-nodes between tumor locations were assessed with Kruskal-Wallis tests. Linear regressions were fitted to assess whether left or right location, compared to the remaining locations grouped, was associated to the percentage and number of positive ipsilateral lymph-nodes., Results: 239 patients were included. The number of ipsilateral positive lymph nodes was superior in right-sided tumors when compared to the rest of the bladder (0, I.Q.R. 0-1 vs. 0, I.Q.R. 0-0, P = 0.047), as well as the percentage of ipsilateral positive lymph-nodes (0, I.Q.R. 0-14.3 vs. 0, I.Q.R. 0-3.7, P = 0.042). The number of ipsilateral positive lymph-nodes in left-sided tumors was superior when compared to the rest of the bladder (0, I.Q.R. 0-1 vs. 0, I.Q.R. 0-0, P = 0.02), as well as the percentage (0, I.Q.R. 0-13.7 vs. 0, I.Q.R. 0-0, P = 0.036). At linear regression analyses, right- and left-sided tumors were associated with an increased percentage of ipsilateral positive lymph-nodes (P = 0,019 and P = 0,003) out of the total ipsilateral lymph-nodes excised., Conclusions: Lateral wall tumor location at diagnostic TURBT (either right or left side) predicts a higher percentage of ipsilateral positive lymph-nodes s/p RC., Competing Interests: Declaration of competing interest All co-authors have no direct or indirect commercial financial incentive associated with publishing the article. Specifically, no financial support has been received for this research/study. No funding agreement limits our ability to complete and publish our research/study fairly, (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)
- Published
- 2024
- Full Text
- View/download PDF
17. Management of penile varicosity in Klippel-Trenaunay-Weber syndrome: a case report.
- Author
-
Brancelli C, Costantino S, Migliorini F, Fracasso P, Roggero L, Baielli A, De Bon L, Fumanelli F, Porcaro AB, Veccia A, Cerruto MA, Bertolo R, and Antonelli A
- Published
- 2024
- Full Text
- View/download PDF
18. Outcomes of da Vinci® versus Hugo RAS® radical prostatectomy: focus on postoperative course, pathological findings, and patients' health-related quality of life after 100 consecutive cases (the COMPAR-P prospective trial).
- Author
-
Antonelli A, Veccia A, Malandra S, Rizzetto R, Artoni F, Fracasso P, Fumanelli F, Palumbo I, Raiti A, Roggero L, Treccani LP, Vetro V, DE Marco V, Porcaro AB, Cerruto MA, Brunelli M, and Bertolo R
- Subjects
- Aged, Humans, Male, Middle Aged, Postoperative Complications epidemiology, Postoperative Complications etiology, Prospective Studies, Treatment Outcome, Prostatectomy methods, Prostatic Neoplasms surgery, Prostatic Neoplasms pathology, Quality of Life, Robotic Surgical Procedures
- Abstract
Background: This study aims to prospectively compare the outcomes of robot-assisted radical prostatectomy (RARP) performed using the Hugo RAS and da Vinci Xi systems, focusing on the postoperative course, pathological findings, and health-related quality of life., Methods: The COMPAR-P trial, a prospective post-market study (clinical-trials.org NCT05766163), commenced in March 2023, enrolling patients for RARP performed with either da Vinci or Hugo RAS without selection criteria for up to 50 consecutive cases per system. Two experienced console surgeons performed the procedures according to a standardized technique. The study evaluated differences between da Vinci and Hugo RAS regarding the postoperative course, pathology findings, 30-day PSA value, functional metrics, and health-related quality of life using SF-36 and University of California Los Angeles Prostate Cancer Index questionnaires., Results: Fifty patients underwent DV-RARP and H-RARP each. Postoperative complications, pathological data, and quality of life metrics did not significantly differ between the groups. Noteworthy limitations include the comparison between the first 50 H-RARP and last 50 DV-RARP cases, as well as the potential influence of surgeons' specialized expertise on the generalizability of findings., Conclusions: This prospective study of 100 unselected patients undergoing RARP with either da Vinci or Hugo RAS systems reveals comparable outcomes in postoperative course, pathology, functional metrics, and health-related quality of life. However, further research with larger sample sizes, longer follow-up periods, and diverse surgical expertise is essential to validate these findings and better understand the implications for clinical practice.
- Published
- 2024
- Full Text
- View/download PDF
19. The 2012 Briganti nomogram predicts disease progression after surgery in high-risk prostate cancer patients.
- Author
-
Porcaro AB, Panunzio A, Orlando R, Tafuri A, Gallina S, Bianchi A, Serafin E, Mazzucato G, Montanaro F, Baielli A, Artoni F, Ditonno F, Roggero L, Franceschini A, Boldini M, Treccani LP, Veccia A, Rizzetto R, Brunelli M, De Marco V, Siracusano S, Cerruto MA, Bertolo R, and Antonelli A
- Abstract
Objectives: We tested whether the 2012 Briganti nomogram for the risk of pelvic lymph node invasion (PLNI) may represent a predictor of disease progression after surgical management in high-risk (HR) prostate cancer (PCa) patients according to the European Association of Urology., Methods: Between January 2013 and December 2021, HR PCa patients treated with robot-assisted radical prostatectomy (RARP) and extended pelvic lymph node dissection (ePLND) were identified. The 2012 Briganti nomogram was evaluated as a continuous and categorical variable, which was dichotomized using the median. The risk of disease progression, defined as the event of biochemical recurrence and/or local recurrence/distant metastases was assessed by Cox regression models., Results: Overall, 204 patients were identified. The median 2012 Briganti nomogram score resulted 12.0% (IQR: 6.0-22.0%). PLNI was detected in 57 (27.9%) cases. Compared to patients who had preoperatively a 2012 Briganti nomogram score ≤12%, those with a score >12% were more likely to present with higher percentage of biopsy positive cores, palpable tumors at digital rectal examination, high-grade cancers at prostate biopsies, and unfavorable pathology in the surgical specimen. At multivariable Cox regression analyses, disease progression, which occurred in 85 (41.7%) patients, was predicted by the 2012 Briganti nomogram score (HR: 1.02; 95%CI: 1.00-1.03; p = 0.012), independently by tumors presenting as palpable (HR: 1.78; 95%CI: 1.10.2.88; p = 0.020) or the presence of PLNI in the surgical specimen (HR: 3.73; 95%CI: 2.10-5.13; p = 0.012)., Conclusions: The 2012 Briganti nomogram represented an independent predictor of adverse prognosis in HR PCa patients treated with RARP and ePLND. As the score increased, so patients were more likely to experience disease progression, independently by the occurrence of PLNI. The association between the nomogram, unfavorable pathology and tumor behavior might turn out to be useful for selecting a subset of patients needing different treatment paradigms in HR disease., Competing Interests: No potential conflict of interest was reported by the author(s)., (© 2024 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.)
- Published
- 2024
- Full Text
- View/download PDF
20. Intraoperative Performance of DaVinci Versus Hugo RAS During Radical Prostatectomy: Focus on Timing, Malfunctioning, Complications, and User Satisfaction in 100 Consecutive Cases (the COMPAR-P Trial).
- Author
-
Antonelli A, Veccia A, Malandra S, Rizzetto R, De Marco V, Baielli A, Franceschini A, Fumanelli F, Montanaro F, Palumbo I, Pettenuzzo G, Roggero L, Angela Cerruto M, and Bertolo R
- Abstract
Background and Objective: The Hugo RAS and DaVinci Xi systems are used for performing robot-assisted radical prostatectomy (RARP). This study aims to compare these two platforms providing granular and comprehensive data on their intraoperative performance., Methods: The Comparison of Outcomes of Multiple Platforms for Assisted Robotic surgery-Prostate (COMPAR-P) trial is a prospective post-market study (clinicaltrials.org NCT05766163). Enrollment began in March 2023, allocating patients to DaVinci or Hugo RAS for RARP, without selection criteria, for up to 50 consecutive cases. Two experienced console surgeons performed the procedures, following the same technique. Evaluation focused on timing, learning curves, malfunctioning events, complications, and users' satisfaction, using standard statistical methods, including the cumulative summation analysis (CUSUM) for the learning curve assessment., Key Findings and Limitations: Fifty patients each were enrolled for DaVinci (DV-RARP) and Hugo RAS (H-RARP) RARP. Baseline features were balanced. DV-RARP showed significantly shorter "setup" and "console" phase durations than H-RARP (37 vs 55 min and 97 vs 126 min, respectively, p < 0.001). A longitudinal timing analysis revealed DV-RARP's flat line, while H-RARP showed a modest decline with breakpoints at 22 and 17 procedures by CUSUM for the setup and console phases. The numbers of malfunctioning events were 4 (DV-RARP) and 20 (H-RARP). DV-RARP had high user satisfaction, while the user satisfaction of H-RARP varied. The comparison was between the first 50 H-RARP and the last 50 DV-RARP cases performed at our institution. This likely accounts for the observed differences in setup and console times between the cohorts. The specialized expertise of the surgeons involved could limit the generalizability of our findings., Conclusions and Clinical Implications: This prospective study compared unselected patients who underwent DV-RARP and H-RARP. More malfunctioning events occurred in case of Hugo RAS, but surgical outcomes were similar. Longer operative times for Hugo RAS were attributed to meticulous care with the novel platform. Improvement potential was evident within a few procedures, providing valuable insights for adopting this new platform., Patient Summary: This study compared two advanced robotic systems, DaVinci and Hugo RAS, used to remove the prostate in patients diagnosed with prostate cancer. While both systems showed similar surgical outcomes, the newer Hugo RAS system required more meticulous movements, leading to slightly longer operation times. The findings suggest that, with further experience, both systems can provide effective treatment options for patients undergoing prostate surgery., (© 2024 The Author(s).)
- Published
- 2024
- Full Text
- View/download PDF
21. Prevalence and clinical significance of ANCA positivity in lupus nephritis: a case series of 116 patients and literature review.
- Author
-
Lacetera R, Calatroni M, Roggero L, Radice A, Pozzi MR, Reggiani F, Sciascia S, Trezzi B, Roccatello D, Minetti E, Moroni G, and Sinico RA
- Subjects
- Humans, Antibodies, Antineutrophil Cytoplasmic, Retrospective Studies, Clinical Relevance, Prevalence, Lupus Nephritis diagnosis, Lupus Nephritis drug therapy, Lupus Nephritis epidemiology
- Abstract
The prevalence and clinical significance of anti-neutrophil cytoplasmic antibodies [ANCAs] in patients with lupus nephritis [LN] is not fully elucidated. Our aim was to determine whether LN patients with ANCA positivity had different clinicopathological features and outcomes compared to ANCA-negative patients., Methods: Among our LN patients we retrospectively selected those who underwent ANCA testing the day of the kidney biopsy and before the start of induction treatment. Clinical/histopathological features at kidney biopsy and renal outcome of ANCA-positive patients were compared with those of ANCA-negative subjects., Results: We included 116 Caucasian LN patients in the study; 16 patients [13.8%] were ANCA-positive. At kidney biopsy, ANCA-positive patients presented more frequently with an acute nephritic syndrome than ANCA-negative ones; the difference however does not reach statistical significance [44 vs. 25%, p = 0.13]. At histological evaluation, proliferative classes [100% vs 73%; p = 0.02], class IV [68.8% vs 33%; p < 0.01] and necrotizing tuft lesions [27 vs 7%, p = 0.04] were more frequent, and the activity index was higher [10 vs 7; p = 0.03] in ANCA-positive than in ANCA-negative patients. Despite worse histological features, after a 10-year observation period, there were no significant differences in the number of patients with chronic kidney function impairment (defined as eGFR < 60 mL/min per 1.73 m
2 ) between the ANCA-positive and negative groups [24.2 vs 26.6%, p = 0.9]. This could be the result of the more aggressive therapy, with rituximab plus cyclophosphamide, that ANCA-positive patients received more frequently than ANCA-negative ones [25 vs. 1.3%, p < 0.01]., Conclusions: ANCA-positive LN patients frequently have histological markers of severe activity (proliferative classes and high activity index) that require timely diagnosis and aggressive therapy to limit the development of irreversible chronic kidney damage., (© 2023. The Author(s) under exclusive licence to Italian Society of Nephrology.)- Published
- 2023
- Full Text
- View/download PDF
22. Erratum to: Relapsing Minimal Change Disease Superimposed on Late-Onset p.N215S Fabry Nephropathy.
- Author
-
Salerno FR, Roggero L, Rossi F, Binaggia A, Bertoli S, and Pieruzzi F
- Abstract
[This corrects the article DOI: 10.1093/ckj/sfab148.]., (© The Author(s) 2022. Published by Oxford University Press on behalf of the ERA.)
- Published
- 2022
- Full Text
- View/download PDF
23. Relapsing minimal change disease superimposed on late-onset p.N215S Fabry nephropathy.
- Author
-
Salerno FR, Roggero L, Rossi F, Binaggia A, Bertoli S, and Pieruzzi F
- Abstract
We present the case of a 76-year-old man with late-onset Fabry disease caused by the p.N215S missense mutation, with Fabry cardiomyopathy and nephropathy. In this case, the diagnosis of Fabry disease was incidental and followed minimal change disease (MCD) onset, with nephrotic syndrome and acute kidney injury requiring renal replacement therapy. Fabry nephropathy associated with the p.N215S mutation is becoming increasingly recognized among older patients. The importance of electron microscopy is herein highlighted and histological features common to Fabry nephropathy and MCD are discussed, along with the challenges associated with the diagnosis and clinical management., (© The Author(s) 2021. Published by Oxford University Press on behalf of ERA-EDTA.)
- Published
- 2021
- Full Text
- View/download PDF
24. Elevated Ambulatory Blood Pressure Measurements are Associated with a Progressive Form of Fabry Disease.
- Author
-
Rossi F, Svarstad E, Elsaid H, Binaggia A, Roggero L, Auricchio S, Marti HP, and Pieruzzi F
- Subjects
- Adult, Aged, Disease Progression, Fabry Disease physiopathology, Female, Humans, Hypertension physiopathology, Male, Middle Aged, Blood Pressure, Blood Pressure Monitoring, Ambulatory, Fabry Disease complications, Hypertension etiology
- Abstract
INTRODUCTION: Published data on hypertension incidence and management in Anderson-Fabry disease are scant and the contribution of elevated blood pressure to organ damage is not well recognized., Aim: Therefore, we have assessed blood pressure values and their possible correlations with clinical findings in a well described cohort of Fabry patients., Methods: Between January 2015 and May 2019, all adult Fabry patients (n = 24 females, n = 8 males) referred to our institute were prospectively enrolled. During the first examination patient's genotype and clinical characteristics were recorded. Blood pressure data were obtained by standard observed office measurements followed, within 6 months, by ambulatory blood pressure monitoring and home self-recordings. Organ involvement, including kidneys, heart and brain, was monitored over time. Consequently, patients were defined as clinically stable or progressive through the Fabry Stabilization Index., Results: The standard office measurements have diagnosed hypertension in three (9.37%) patients, but the ambulatory monitoring showed elevated blood pressure in six (18.75%) patients, revealing three cases of masked hypertension. All the hypertensive patients were females and, compared with normotensive subjects, they presented a lower glomerular filtration rate (p < 0.05) and a more advanced cardiac hypertrophy (p < 0.05). Four (66.7%) of them were diagnosed with a progressive form of the disease through the Fabry Stabilization Index while the majority of the normotensive group (84.6%, n = 19) was stable over time. No correlation was found between the prevalence of hypertension and the type of mutations causing Fabry disease., Conclusion: Hypertension can be found in a restricted portion of clinically stable Fabry patients. In contrast, patients presenting with a progressive organ involvement, particularly renal impairment, have a major risk of developing uncontrolled blood pressure, and should be followed carefully. Moreover, the ambulatory blood pressure monitoring proved to be useful to reveal masked hypertension, which can contribute to the progressive worsening of the organ damage. Therefore, a proper diagnosis and therapy of hypertension may improve the outcome of Fabry patients.
- Published
- 2021
- Full Text
- View/download PDF
25. Occurrence of malignant neoplasia in patients with primary hyperparathyroidism.
- Author
-
Palmieri S, Roggero L, Cairoli E, Morelli V, Scillitani A, Chiodini I, and Eller-Vainicher C
- Subjects
- Adult, Aged, Aged, 80 and over, Female, Humans, Italy epidemiology, Logistic Models, Male, Middle Aged, Parathyroid Hormone blood, Time Factors, Vitamin D blood, Hyperparathyroidism, Primary complications, Neoplasms epidemiology
- Published
- 2017
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.