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Microscopic polyangiitis: a rare ANCA-associated small- vessel vasculitis
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2008; 18 (12): 771-773
in English | 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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Index: IMEMR (Eastern Mediterranean) Main subject: Polyarteritis Nodosa / Skin / Autoimmune Diseases / Churg-Strauss Syndrome / Granulomatosis with Polyangiitis / Antibodies, Antineutrophil Cytoplasmic / Diagnosis, Differential Type of study: Case report Limits: Female / Humans Language: English Journal: J. Coll. Physicians Surg. Pak. Year: 2008

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Index: IMEMR (Eastern Mediterranean) Main subject: Polyarteritis Nodosa / Skin / Autoimmune Diseases / Churg-Strauss Syndrome / Granulomatosis with Polyangiitis / Antibodies, Antineutrophil Cytoplasmic / Diagnosis, Differential Type of study: Case report Limits: Female / Humans Language: English Journal: J. Coll. Physicians Surg. Pak. Year: 2008