Microscopic polyangiitis: a rare ANCA-associated small- vessel vasculitis
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2008; 18 (12): 771-773
em Inglês
| IMEMR
| ID: emr-143386
ABSTRACT
Microscopic Polyangiitis [MPA] is an autoimmune disease characterized by pauci-immune, necrotizing, small-vessel vasculitis without clinical or pathological evidence of necrotizing granulomatous inflammation. Because many different organ systems may be involved, a wide range of symptoms are possible in MPA. Cutaneous involvement is not frequent. We describe a young girl who presented with multiple vasculitic skin lesions along with arthralgia and after the onset of illness it took 4 years for appropriate diagnosis and management of the disease
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Índice:
IMEMR (Mediterrâneo Oriental)
Assunto principal:
Poliarterite Nodosa
/
Pele
/
Doenças Autoimunes
/
Síndrome de Churg-Strauss
/
Granulomatose com Poliangiite
/
Anticorpos Anticitoplasma de Neutrófilos
/
Diagnóstico Diferencial
Tipo de estudo:
Relato de Casos
Limite:
Feminino
/
Humanos
Idioma:
Inglês
Revista:
J. Coll. Physicians Surg. Pak.
Ano de publicação:
2008
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