Results 101 to 110 of about 23,505 (244)

IgA Vasculitis with Simultaneous Cardiopulmonary Involvement

Internal Medicine, 2018
A 60-year-old man with a history of hypertension, type 2 diabetes, and reflux esophagitis was admitted to our hospital with hemoptysis, dyspnea, and leg edema. We diagnosed him with adult IgA vasculitis based on the presence of purpura, elevated serum IgA fibronectin complexes, pathophysiological findings, a skin biopsy showing leukocytoclastic ...
Kazunori Bando, Hirofumi Maeba, Ichiro Shiojima   +2 more
openaire   +3 more sources

Immune Complex Small-Vessel Vasculitis with Kidney Involvement [PDF]

, 2018
The term immune complex small-vessel vasculitis encompasses anti-glomerular basement membrane disease, cryoglobulinemic vasculitis, IgA vasculitis and hypocomplementemic urticarial vasculitis. These disorders affect predominantly small vessels, and renal
Boletis, John N., Lionaki, Sophia, Marinaki, Smaragdi, Skalioti, Chrysanthi   +3 more
core   +1 more source

Pediatric Autoimmune Pancreatitis: Clinical Findings and Outcomes in Sweden

United European Gastroenterology Journal, Volume 13, Issue 5, Page 819-830, June 2025.
ABSTRACT Introduction Pediatric autoimmune pancreatitis (AIP) is a rare form of pancreatitis in children with poorly understood pathophysiology. It is a recognized risk factor for chronic pancreatitis in approximately 4% of pediatric cases. This study aims to describe the demographics, clinical characteristics, and outcomes of a large Swedish cohort of
Miroslav Vujasinovic, Fredrik Lindgren, Nikolaos Kartalis, Raffaella Pozzi Mucelli, Dawid Rutkowski, Alexander Waldthaler, Poya Ghorbani, Carlos Fernández Moro, Thomas Casswall, J.‐Matthias Löhr   +9 more
wiley   +1 more source

The profile and clinical outcomes of patients with renal involvement due to IgA vasculitis: is azathioprine a good option for treatment?

Advances in Rheumatology, 2019
Background The Henoch-Schönlein Purpura (HSP) orIgA vasculitis is the most common vasculitis of childhood and may occur with renal involvement, with hematuria and / or proteinuria, and may cause severe and non-reversible sequelae. Objectives To establish
Vânia Schinzel, Jade Dib Fernandez, Gleice Clemente, Melissa Mariti Fraga, Maria Cristina Andrade, Claudio Arnaldo Len, Maria Teresa Terreri   +6 more
doaj   +1 more source

Navigating the initial diagnosis and management of adult IgA vasculitis: A reviewCapsule Summary

JAAD International, 2022
Background: IgA vasculitis in adults has not been thoroughly studied. This has left a practice gap related to the management and follow-up of a population that is at an increased risk of comorbidities and potentially poor outcomes. For this reason, it is
Brenna G. Kelly, BA, Delaney B. Stratton, PhD, DNP, FNP-BC, Iyad Mansour, MD, Bekir Tanriover, MD, MPH, MBA, Keliegh S. Culpepper, MD, Clara Curiel-Lewandrowski, MD   +5 more
doaj  

Púrpura de Henoch-Schönlein Associada a Adenocarcinoma do Pulmão [PDF]

, 2015
Introduction: The Henoch-Schönlein purpura (HSP) is an immunoglobulin A (IgA)-mediated smallvessel systemic vasculitis, rare in adults. The association with solid tumours has been described, especially with lung cancer. Case Report: We present the case
Azevedo, A, Carvalho, F, Fernandes, V, Ferreira, AC, Navarro, D, Nolasco, F, Sousa, J, Viana, H   +7 more
core  

Prognostic Scoring in IgA Vasculitis.

Clin J Am Soc Nephrol
Glassock RJ.
europepmc   +3 more sources

Clinical Characteristics and Treatment Patterns of Children and Adults With IgA Nephropathy or IgA Vasculitis: Findings From the CureGN Study [PDF]

, 2018
Introduction: The Cure Glomerulonephropathy Network (CureGN) is a 66-center longitudinal observational study of patients with biopsy-confirmed minimal change disease, focal segmental glomerulosclerosis, membranous nephropathy, or IgA nephropathy (IgAN)
Ambruzs, Josephine M., Appel, Gerald B., Bomback, Andrew S., Cai, Yi, Cattran, Daniel C., Chishti, Aftab S., CureGN Consortium, D’Agati, Vivette D., D’Alessandri-Silva, Cynthia J., Falk, Ronald J., Flessner, Michael, Gbadegesin, Rasheed A., Gharavi, Ali G., Gillespie, Brenda W., Gipson, Debbie S., Greenbaum, Larry A., Guay-Woodford, Lisa M., Hogan, Jonathan J., Holzman, Lawrence B., Iragorri, Sandra, Jennette, J. Charles, Julian, Bruce A., Khalid, Myda, Kiryluk, Krzysztof, Kretzler, Matthias, Lafayette, Richard A., Liapis, Helen, Lugani, Francesca, Mansfield, Sarah A., Mason, Sherene, Matar, Raed Bou, Nachman, Patrick H., Nast, Cynthia C., Nester, Carla M., Noone, Damien G., Novak, Jan, O’Shaughnessy, Michelle M., Reich, Heather N., Rheault, Michelle N., Rizk, Dana V., Robinson, Bruce M., Saha, Manish K., Sanghani, Neil S., Selewski, David T., Smoyer, William E., Sperati, C. John, Sreedharan, Rajasree, Srivastava, Tarak, Swiatecka-Urban, Agnieszka, Twombley, Katherine, Vasylyeva, Tetyana L., Weaver, Donald J., Yin, Hong, Zee, Jarcy   +53 more
core   +1 more source

Interacción entre inmunodeficiencia y enfermedad autoinmune [PDF]

, 2019
En la literatura actual, existen evidencias de que las enfermedades autoinmunes sistémicas y las inmunodeficiencias no son enfermedades separadas, sino que son entidades enlazadas.
Gómez López, Lucía
core  

Clinical features and pathogenesis of membranoproliferative glomerulonephritis: a nationwide analysis of the Japan renal biopsy registry from 2007 to 2015 [PDF]

, 2018
BackgroundThe incidence and age distribution of membranoproliferative glomerulonephritis (MPGN) vary throughout the world by race and ethnicity. We sought to evaluate the clinical features, pathogenesis, and age distribution of MPGN among a large ...
Hasebe Naoyuki, Hattori Motoshi, Isaka Yoshitaka, Maruyama Shoichi, Nagata Michio, Nakagawa Naoki, Narita Ichiei, Sato Hiroshi, Shimizu Akira, Sugiyama Hitoshi, Yokoyama Hitoshi, 長田 道夫   +11 more
core   +2 more sources