Results 21 to 30 of about 601 (132)

Edema hemorrágico agudo da infância: uma variante da púrpura de Henoch-Schönlein? Acute hemorrhagic edema of infancy: a variant of Henoch-Schönlein purpura?

open access: yesRevista Brasileira de Reumatologia, 2007
O edema hemorrágico agudo da infância (EHAI) é uma vasculite leucocitoclástica rara, com aproximadamente 100 casos descritos na literatura de língua inglesa.
Christina Feitosa Pelajo   +1 more
doaj   +1 more source

Hemorrhagic Intestinal Henoch‐Schonlein Purpura Complicated by Cytomegalovirus Infection

open access: yesCanadian Journal of Gastroenterology and Hepatology, Volume 12, Issue 1, Page 71-74, 1998., 1998
A 54‐year‐old man on hemodialysis for acute chronic renal failure and on corticosteroids for Henoch‐Schonlein purpura developed massive hematochezia. After extensive clinical investigation, an ileal bleeding site was identified and surgically removed. Pathological examination of the diseased bowel segment revealed an extensive vasculitis with mucosal ...
Phong Nguyen-Ho   +2 more
wiley   +1 more source

Polyarteritis Nodosa and Bronchiolitis Obliterans with Organizing Pneumonia, an Unusual Association

open access: yesCanadian Respiratory Journal, Volume 4, Issue 4, Page 221-223, 1997., 1997
Bronchiolitis obliterans and organizing pneumonia (BOOP) is an inflammatory, fibrotic disorder of the small airways, alveoli and pulmonary intersitium. Often idiopathic and usually benign, this condition may cause dyspnea and influenza‐like symptoms. Polyarteritis nodosa (PAN) is a small and medium vessel vasculitis, which usually involves the kidney ...
Kaberi Dasgupta   +2 more
wiley   +1 more source

Lúpus eritematoso sistêmico complicado por vasculite intestinal e pneumatose intestinal Systemic lupus erythematosus complicated by intestinal vasculitis and pneumatosis intestinalis

open access: yesRevista Brasileira de Reumatologia, 2010
As manifestações gastrointestinais no lúpus eritematoso sistêmico (LES) não são incomuns. Frequentemente são encontrados sintomas inespecíficos, como dor abdominal, náuseas, vômitos e diarreia.
Débora Karine Marinello   +3 more
doaj   +1 more source

Crohn’s Disease – The Pathogenesis of a Granulomatous Vasculitis: A Hypothesis

open access: yesCanadian Journal of Gastroenterology and Hepatology, Volume 9, Issue 4, Page 199-202, 1995., 1995
Dissatisfied with traditional approaches to studying the pathogenesis of Crohn’s disease, the author and colleagues proposed and developed the hypothesis that Crohn’s disease is a granulomatous vasculitis mediated by a persistent viral infection of the mesenteric microvascular endothelium.
Andrew J Wakefield
wiley   +1 more source

Doença de Takayasu com grave envolvimento cardíaco e arterial em pré-escolar

open access: yesArquivos Brasileiros de Cardiologia, 2010
Neste artigo os autores descrevem um caso de arterite de Takayasu em uma criança de apenas 3 anos de idade, ressaltando-se a raridade dessa doença nessa faixa etária.
Fátima Derlene da Rocha Araújo   +4 more
doaj   +1 more source

Granulomatous Vasculitis and Persistent Measles Virus Infection in Crohn’s Disease

open access: yesCanadian Journal of Gastroenterology and Hepatology, Volume 8, Issue 2, Page 70-74, 1994., 1994
Based upon the recent observation of vasculitis in Crohn’s disease, a process that is more widespread than was recognized previously, the author investigated the possibility that this mechanism may provide an explanation for some of the clinical and histological idiosyncracies of this condition.
AJ Wakefield
wiley   +1 more source

Displasia fibromuscular: um diagnóstico diferencial para as vasculites Fibromuscular dysplasia: a differential diagnosis of vasculitis

open access: yesRevista Brasileira de Reumatologia, 2012
A displasia fibromuscular (DFM) envolve artérias de pequeno e médio calibre e é uma causa bem conhecida de hipertensão em mulheres jovens caucasianas, quando envolve as artérias renais.
Thaís de Carvalho Pontes   +4 more
doaj   +1 more source

Wound chronicity and fibroblast senescence – implications for treatment

open access: yesInternational Wound Journal, Volume 2, Issue 4, Page 336-339, December 2005., 2005
Chronicite de la plaie et senescence fibroblastique_implications therapeutiques Une certaine proportion de plaies chroniques ne cicatrise pas après un traitement standard. Pour les ulcers veineux une corrélatione xiste entre un début de traitement tardif et une mauvaise réponse cicatritielle au traitement par compression.
wiley   +1 more source

Epistaxis como primeira manifestação de granulomatose Wegener. Caso clínico

open access: yesRevista Portuguesa Otorrinolaringologia e Cirurgia de Cabeça e Pescoço, 2010
A Granulomatose de Wegener é uma doença sistémica de etiologia desconhecida, caracterizada pela tríade clínica: envolvimento da mucosa nasal e dos seios perinasais, infiltração e cavitação pulmonar e doença renal com hematúria.
A. Casas Novas   +3 more
doaj   +1 more source

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