Results 21 to 30 of about 5,195 (226)

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

Revista 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, Geísa Pereira Rufino, Mariana Galvão Gurgel, Arnaldo Correia de Medeiros, Eutília Andrade Medeiros Freire   +4 more
doaj   +1 more source

Idiopathic retinal, vasculitis, aneurysms and neuroretinitis (IRVAN): case report [PDF]

, 2012
A case of a 14 year-old boy that was admitted complaining of bilateral ocular visual blurring for 2 years is reported. The ophthalmological examination disclosed bilateral mild optic disc hyperemia and swelling, retinal exudation, few retinal hemorrhages,
Arantes, Tiago Eugênio Faria e, Lima, Verônica Castro, Matos, Kimble Teixeira Fonseca, Muccioli, Cristina, Rodrigues, Kelly Fernandes de Paula   +4 more
core   +3 more sources

Epistaxis como primeira manifestação de granulomatose Wegener. Caso clínico

Revista 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, I. Moreira, P. Brazão Santos, L. Monteiro   +3 more
doaj   +1 more source

Inflammatory Bowel Disease with Cytoplasmic‐Staining Antineutrophil Cytoplasmic Antibody and Extensive Colitis

Canadian Journal of Gastroenterology and Hepatology, Volume 12, Issue 4, Page 279-282, 1998., 1998
A cohort of 18 patients with inflammatory bowel disease who were characterized by the presence of cytoplasmic‐staining antineutrophil cytoplasmic antibody (cANCA) and extensive colitis is reported. Almost half were Indo‐Canadians, and atypical perinuclear‐staining antineutrophil cytoplasmic antibody was also detected in five (28%), similar to the ...
Hugh James Freeman
wiley   +1 more source

Síndrome de Behçet: à procura de evidências Behçet's syndrome: looking for evidences

Revista Brasileira de Reumatologia, 2006
A síndrome de Behçet (SB) é uma afecção inflamatória multissistêmica, de acometimento vascular e de causa ainda desconhecida, basicamente caracterizada por úlceras orais e genitais recorrentes, uveíte e lesões cutâneas.
Fabrício de Souza Neves, Júlio César Bertacini de Moraes, Célio Roberto Gonçalves   +2 more
doaj   +1 more source

Midbrain vasculitic aneurysms [PDF]

Neurology, 2004
This 16-year-old girl had a muscle biopsy demonstrating vasculitis seven years ago when she presented with weakness and Raynaud’s phenomenon (figure, B). Aside from occasional unexplained abdominal pain and chronic anemia, she had been well until one year ago, …
Hyung-Min, Kwon, Jae-Kyu, Roh, Gregory Youngnam, Chang   +2 more
openaire   +2 more sources

Hemorrhagic Intestinal Henoch‐Schonlein Purpura Complicated by Cytomegalovirus Infection

Canadian 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, Laurence D Jewell, Alan BR Thomson   +2 more
wiley   +1 more source

Hipertensão arterial pulmonar e acidente vascular encefálico em paciente com Arterite de Takayasu Pulmonary arterial hypertension and cerebrovascular disease in patient with Takayasu Arteritis

Revista Brasileira de Reumatologia, 2006
Arterite de Takayasu (AT) é uma doença rara caracterizada por vasculite dos grandes vasos, principalmente aorta e seus ramos. A inflamação vascular leva a irregularidades na parede do vaso, causando estenoses e aneurismas.
Carlos Frederico Rodrigues Parchen, Carolina de Souza Müller, Salun Aragão, Eduardo Santos Paiva, Sebastião Radominski   +4 more
doaj   +1 more source

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

Canadian 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, A Kevin Watters, Arnold Zidulka   +2 more
wiley   +1 more source

Síndrome de Behçet e policondrite recidivante: síndrome MAGIC Behçet's syndrome and relapsing polychondritis: MAGIC syndrome

Revista Brasileira de Reumatologia, 2006
Relatamos aqui o caso de um paciente masculino de 30 anos de idade, sexo masculino, com achados clínicos típicos da síndrome de Behçet (SB) e da policondrite recidivante (PR) sem, no entanto, preencher completamente os critérios de classificação para ...
Fabrício de Souza Neves, Deborah Pereira Gonçalves, Laís V. Lage, Célio Roberto Gonçalves   +3 more
doaj   +1 more source