Results 31 to 40 of about 56,061 (148)

A challenging case on diagnosing Henoch–Schönlein purpura

European Journal of Inflammation, 2020
Henoch–Schönlein purpura (HSP) could involve multiple organs, including gastrointestinal tract. It is commonly observed in children, but occasionally also in the elderly. It is challenging to diagnose HSP with delayed purpura.
Lin-Hao Zhang, Tian Lan, Du He, Shi-Lei Wen, Huan Tong   +4 more
doaj   +1 more source

Henoch-Schönlein Nephritis Manifesting with Purpura 15 years after Diagnosis of IgA Nephropathy

Case Reports in Nephrology, 2019
Henoch-Schönlein nephritis or immunoglobulin A (IgA) vasculitis is characterized by purpura, arthralgia, abdominal pain, and glomerulonephritis with glomerular IgA deposition. Notably, the presence of purpura is essential to diagnose this disease.
Hideaki Yamabe, Mitsuaki Kaizuka, Satoru Tsunoda, Tasuku Nagasawa, Kazuo Nomura, Michiko Shimada   +5 more
doaj   +1 more source

Henoch-Schönlein nephritis associated with streptococcal infection and persistent hypocomplementemia: a case report

Journal of Medical Case Reports, 2010
Introduction Henoch-Schönlein purpura is a systemic disease with frequent renal involvement, characterized by IgA mesangial deposits. Streptococcal infection can induce an abnormal IgA immune response like Henoch-Schönlein purpura, quite similar to ...
Vozmediano María C, de la Nieta Maria, Pérez-Álvarez Javier, Anaya Sara, Rivera Francisco, Blanco Julia   +5 more
doaj   +1 more source

Protein-losing enteropathy associated with Henoch-Schönlein purpura

Pediatric Reports, 2010
The gastrointestinal manifestations of Henoch-Schönlein purpura include abdominal pain, gastrointestinal bleeding, intussusception, and perforation. Protein-losing enteropathy is rarely associated with Henoch-Schönlein purpura.
Ayako Nakamura, Tatsuo Fuchigami, Yasuji Inamo   +2 more
doaj   +1 more source

Henoch-Schönlein purpura fulminant

Acta Médica del Centro, 2015
A female patient of 51 years old with personal pathological precedent of bronchial asthma, hypertension and ulcerative colitis and infection by chikungunya virus for a month.
Daniel Artiles Martínez, Arletis Ferrer Pérez, Johamel Ramos Valdés, Lisbetty López Gonzalez, Pedro Alberto Marrero García, Merlyn Arce Nuñez, Osbel Quintana Morales, Miguel Fernández Olivares, Lázaro Vázquez Gómez, Juan Humberto Gutiérrez Ronquillo   +9 more
doaj  

CIANOSE E PÚRPURA NOS QUIRODÁCTILOS − FUNDAMENTOS DO DIAGNÓSTICO DIFERENCIAL, A PROPÓSITO DE UM CASO

Revista da Sociedade Portuguesa de Dermatologia e Venereologia, 2015
As púrpuras e a cianose são lesões elementares frequentemente vistas por médicos de diversas especialidades. Suas causas podem variar de doenças raras, como trombofilias, a traumatismos ocupacionais.
Fred Bernardes Filho, Bianca Passos Leite dos Santos, Marjorie Soares Pereira Gonçalves, Suzana Mary de Carvalho, Viviane Vargas dos Santos   +4 more
doaj   +1 more source

PÚRPURA DE HENOCH-SCHÖNLEIN/ VASCULITE POR IMUNOGLOBULINA A: RELATO DE CASO [PDF]

, 2020
Rayra Carvalho Maia, Cláudio Arnaldo Len, Karina Rinaldo   +2 more
openalex   +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  

Clínica neurológica como inicio de una púrpura trombótica trombocitopénica [PDF]

, 2004
Esther Álvarez-Rodríguez, J. L. M. GARCÍA, Raquel Torres Gárate, Janira Navarro, M. Romero Sánchez, María Abad Cardiel   +5 more
openalex   +1 more source

The Relationship Between Helicobacter Pylori Infection And Childhood Idiopathic Thrombocytopenic Purpura

مجلة كلية الطب, 2007
Background: Idiopathic thrombocytopenic purpura , a disorder characterized by autoantibody mediated platelets destruction causing decreased number of circulating platelets manifest as bleeding tendency.
Sawsan S. Abbas, Tariq M. Hadi
doaj