Systemic Clinical Manifestations and Treatment of Granulomatosis with Polyangiitis: A Case Report

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Ang Wei Chern; Sriraman Malathi

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Journal Paper

Paper Information

Journal: JOURNAL OF PHARMACEUTICAL CARE Year:2018 | Volume:6 | Issue:1-2 Page(s): 34-36

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Information Journal Paper

Title

Systemic Clinical Manifestations and Treatment of Granulomatosis with Polyangiitis: A Case Report

Author(s)

Ang Wei Chern | Sriraman Malathi | Issue Writer Certificate

Keywords

Granulomatosis with Polyangiitis

Immunosuppression

Anti-Infective Agents

Granuloma

Abstract

Granulomatosis with Polyangiitis/fa?page=1&sort=1&ftyp=all&fgrp=all&fyrs=all" target="_blank">Granulomatosis with Polyangiitis (GPA) is a Granulomatous disorder linked with systemic necrotizing vasculitis with varied initial manifestations. We describe a case of a 49-year-old Malay female patient who gradually developed more symptoms of GPA over the past 14 years. This case emphasizes early detection and optimal treatment to minimize any further complications of GPA.

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APA: Copy

Sriraman, Malathi. (2018). Systemic Clinical Manifestations and Treatment of Granulomatosis with Polyangiitis: A Case Report. JOURNAL OF PHARMACEUTICAL CARE, 6(1-2), 34-36. SID. https://sid.ir/paper/350944/en

Vancouver: Copy

Sriraman Malathi. Systemic Clinical Manifestations and Treatment of Granulomatosis with Polyangiitis: A Case Report. JOURNAL OF PHARMACEUTICAL CARE[Internet]. 2018;6(1-2):34-36. Available from: https://sid.ir/paper/350944/en

IEEE: Copy

Malathi Sriraman, “Systemic Clinical Manifestations and Treatment of Granulomatosis with Polyangiitis: A Case Report,” JOURNAL OF PHARMACEUTICAL CARE, vol. 6, no. 1-2, pp. 34–36, 2018, [Online]. Available: https://sid.ir/paper/350944/en

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