Results 51 to 60 of about 6,906 (205)

Anesthetic management of a patient with Henoch-Schonlein purpura for drainage of cervical lymphadenitis: A case report

Saudi Journal of Anaesthesia, 2014
Henoch-Schonlein purpura (HSP) is a multisystem disease and immunoglobulin A-mediated vasculitis with a self-limited course affecting the skin, joints, gastrointestinal tract, and kidneys.
Neha Hasija, Susheela Taxak, Mamta Bhardwaj, Kirti Vashist   +3 more
doaj   +1 more source

Risk of Autoimmune Skin Diseases Associated With Immune Checkpoint Inhibitors: A Pharmacovigilance Analysis Using the FAERS Database

Dermatologic Therapy, Volume 2025, Issue 1, 2025.
Background: Immune checkpoint inhibitors (ICIs) revolutionize cancer therapy but frequently cause immune‐related adverse events (irAEs), with autoimmune skin diseases (ASDs) being significant toxicities requiring careful management. Objective: This study explores the association between ICIs and 10 common ASDs using the FAERS database, aiming to ...
Zi-Yue Dong, Ming-Jie He, Yuan Hu, Imran Majid   +3 more
wiley   +1 more source

HENOCH-SCHONLEIN PURPURA IN CHILDHOOD

Acta Medica Medianae, 2015
were: fever (47.21%), abdominal pain (28.61%), joint pain (25.33%), and muscle pain (18.03%). Changes such as purpura were present on hands (6.5%), forearm (12.3%), lower leg (81.2%), gluteal region (28.13%), and feet (21.35%). We also recorded: leukocytosis (11.37%), thrombocytopenia (7.21%), high level of CRP (6.21%) and high level of serum CPK and ...
Zlatko Đurić, Hristina Stamenkovic, Tatjana Stankovic   +2 more
openaire   +2 more sources

Improving Patient Understanding of Glomerular Disease Terms With ChatGPT

International Journal of Clinical Practice, Volume 2025, Issue 1, 2025.
Background: Glomerular disease is complex and difficult for patients to understand, as it involves various pathophysiology, immunology, and pharmacology areas. Objective: This study explored whether ChatGPT can maintain accuracy while simplifying glomerular disease terms to enhance patient comprehension.
Yasir H. Abdelgadir, Charat Thongprayoon, Iasmina M. Craici, Wisit Cheungpasitporn, Jing Miao, Harry H. X. Wang   +5 more
wiley   +1 more source

Decreased glycolysis induced dysfunction of NK cells in Henoch-Schonlein purpura patients

BMC Immunology, 2020
Background Henoch-Schonlein purpura (HSP) is the most common systemic vasculitis of the childhood. However, its mechanisms and pathogenesis still need more exploration. Natural killer (NK) cells are innate lymphocytes, and there is a growing appreciation
Wenjia Chai, Xiaolin Wang, Wei Wang, Hui Wang, Wenjun Mou, Jingang Gui   +5 more
doaj   +1 more source

Prognostic Utility of the MEST‐C Score Combined With Clinical Parameters in Hispanic Patients With IgA Nephropathy

International Journal of Nephrology, Volume 2025, Issue 1, 2025.
Introduction: The Oxford/MEST‐C classification is a histopathological scoring system for patients with IgA nephropathy (IgAN) that has demonstrated prognostic utility. The aim of this study was to evaluate the prognostic utility of the combination of clinical characteristics and MEST‐C in Hispanic ethnicity patients. Methods: Retrospective cohort study.
Lyzinhawer Alza-Arcila, Esteban Echeverri-Fernández, Mauricio Restrepo-Escobar, Ligia Lorena Calderón, José Manuel Ustáriz, Luis Fernando Arias-Restrepo, Joaquín Roberto Rodelo-Ceballos, David Kershaw   +7 more
wiley   +1 more source

Acute compartment syndrome of the hand in Henoch-Schonlein Purpura

Journal of Medical Case Reports, 2007
An eight year old boy with Henoch-Schonlein Purpura (HSP) presented with acute compartment syndrome (ACS) of his left hand following arterial cannulation of his radial artery in intensive care unit.
Luis Guntur E, Ng Eng-Seng
doaj   +1 more source

IgA vasculitis (Henoch-Schonlein purpura) in children: A Kashmir experience [PDF]

Al Ameen Journal of Medical Sciences, 2021
Background: Immunoglobulin A vasculitis (IgAV) also known as Henoch-Schonlein purpura is a common form of primary vasculitis, characterized clinically by palpable skin rash and one or more gastrointestinal, musculoskeletal, and/or renal system(s ...
Mohd Ashraf, Anisa Riyaz, Sayar Ahmed Bhat, Khurshid Ahmed Wani, Naseer Yousuf Mir, Syed Ashiq Nisar Andrabi, Asma Wani   +6 more
doaj  

Characterisation of IgA Nephropathy in an Australian Cohort

International Journal of Nephrology, Volume 2025, Issue 1, 2025.
Aim: This retrospective cohort study aims to evaluate the prognostic factors for progression of immunoglobulin A nephropathy (IgAN) to kidney failure (defined as the initiation of kidney replacement therapy or death) and all‐cause mortality in an Australian population.
Shriram Swaminathan, Nithya Neelakantan, Henry Bryant, Pimvara Rattanamastip, Gagandeep Sandhu, Bobby Chacko, David Kershaw   +6 more
wiley   +1 more source

Immune or inherited thrombocytopenia? A population‐based cohort study on children and adolescents presenting with a low platelet count

Pediatric Blood &Cancer, Volume 71, Issue 12, December 2024.
Abstract Background Thrombocytopenia is a common hematologic finding in children and adolescents. Immune thrombocytopenia (ITP) is the most common cause of this finding, but the differential diagnosis includes a growing list of genetic disorders.
Lauri‐Matti Kulmala, Henri Aarnivala, Tytti Pokka, Anu Huurre, Liisa Järvelä, Sauli Palmu, Tuuli Pöyhönen, Riitta Niinimäki   +7 more
wiley   +1 more source