Results 41 to 50 of about 27,754 (209)

Multisystem Complications in Non‐Transfusion‐Dependent β‐Thalassemia Intermedia: A Case Highlighting the Need for Early Intervention

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT This case highlights that severe complications of non‐transfusion‐dependent β‐thalassemia may be preventable with appropriate monitoring and timely intervention; however, once established, multisystem complications can be challenging to treat.
Oldooz Aloosh, Seyedeh Esmat Hosseini, Mohammad Karimi   +2 more
wiley   +1 more source

Fulminant Multisystem IgA Vasculitis With Diffuse Alveolar Hemorrhage, Severe Gastrointestinal Hemorrhage, Paralytic Ileus, and Renal Involvement in an Adolescent: A Case Report

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT A 17‐year‐old girl with IgA vasculitis developed diffuse alveolar hemorrhage, severe gastrointestinal hemorrhage with paralytic ileus, and clinical renal involvement. Early bronchoscopy demonstrated diffuse airway bleeding, supported the diagnosis, enabled microbiological sampling, and informed postponement of pharmacological ...
Xianzhang Shan, Yancui Zhu
wiley   +1 more source

Pulmonary involvement in Henoch-Schonlein purpura [PDF]

Emergency Medicine Journal, 2006
A 72-year-old man presented to the emergency department with a 2-day history of fever and difficulty in breathing. His medical history included Henoch–Schonlein purpura treated with steroids, pulmonary tuberculosis treated with antimicrobials, and lobectomy of the right …
A, Soloukides, D-A, Moutzouris, G, Metaxatos, V, Hadjiconstantinou   +3 more
openaire   +2 more sources

Púrpura de henoch-schonlein: revisão bibliográfica e relato de um caso. [PDF]

, 1998
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Pediatria, Curso de Medicina, Florianópolis ...
Minatto, André Caporal
core  

Abdominal pain in pediatric immunoglobulin A vasculitis: Risk factors and severity predictors in a multicenter cohort

Journal of Pediatric Gastroenterology and Nutrition, Volume 83, Issue 3, Page 412-421, September 2026.
Abstract Objectives To identify risk factors for abdominal pain and predictors of complicated abdominal pain in pediatric immunoglobulin A vasculitis (IgAV). Methods Retrospective multicenter study including children and adolescents (≤18 years) fulfilling the European League Against Rheumatism/Pediatric Rheumatology International Trials Organization ...
Francisco Hugo Rodrigues Gomes, Natalia Maronese, Leticia Lizardo Magalhaes, Davi Casale Aragon, Gleice Clemente, Maria Teresa Terreri, Claudio Arnaldo Len, Rozana Gasparello de Almeida, Marta Cristine Felix Rodrigues, Flavio Sztajnbok, Lia Vineyard Steuer, Matheus Santos França, Clovis Artur Almeida da Silva, Virginia Paes Leme Ferriani, Luciana Martins de Carvalho   +14 more
wiley   +1 more source

Bartonella seropositivity in children with Henoch-Schonlein purpura [PDF]

BMC Infectious Diseases, 2005
Abstract Background An association between Henoch-Schonlein purpura (HSP) and seropositivity for Bartonella henselae (BH) has been described. The objective of this study was to see if such an association exists in northern Alberta. Methods
McColl Dorothy, Prasad Errol, Spady Donald W, Robinson Joan L, Artsob Harvey   +4 more
openaire   +3 more sources

Partial response to anakinra in life-threatening Henoch-Schönlein purpura: case report

Pediatric Rheumatology Online Journal, 2011
Henoch-Schönlein purpura is one of the most common forms of systemic vasculitis of childhood. We report the response to anakinra, the interleukin-1 receptor antagonist, in a 9 year old girl without prior medical problems who developed life-threatening ...
Boyer Erynn M, Turman Martin, O'Neil Kathleen M   +2 more
doaj   +1 more source

Cutaneous IgA Vasculitis in Primary Sjögren Disease: Findings From a Medical Record–Based Review

ACR Open Rheumatology, Volume 8, Issue 7, July 2026.
Objective This study aimed to describe clinical observations of patients presenting with palpable purpura, which is suspected to represent IgA vasculitis (IgAV) based on direct immunofluorescence (DIF), who were ultimately diagnosed with cutaneous vasculitis associated with primary Sjögren disease (SjD).
Shay Brikman, Mohammad Egbaria, Amir Bieber   +2 more
wiley   +1 more source

Oxford Classification of IgA Nephropathy Is Applicable to Predict Long-Term Outcomes of Henoch-Schönlein Purpura Nephritis

Iranian Journal of Allergy, Asthma and Immunology, 2014
Henoch-Schönlein purpura nephritis and IgA nephropathy are currently considered to be different clinical presentations of the same disease. There is need for a reliable proven, morphologic classification that can help clinicians more accurately formulate
Hamid Nasri
doaj  

Allergic but not autoimmune comorbidities in children with PFAPA: A nationwide matched case–control cohort study

Pediatric Allergy and Immunology, Volume 37, Issue 7, July 2026.
Abstract Background Periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis (PFAPA) is the most common autoinflammatory syndrome of childhood. Although immune dysregulation is central to its pathogenesis, the broader burden of allergic and autoimmune comorbidities in PFAPA remains incompletely characterized.
Yackov Berkun, Eli Magen, Eugene Merzon, Ilan Green, Avivit Golan‐Cohen, Shlomo Vinker, Ariel Israel   +6 more
wiley   +1 more source