Published August 1, 2018
| Version v1
Journal article
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Systemic Clinical Manifestations and Treatment of Granulomatosis with Polyangiitis: A Case Report
Authors/Creators
- 1. Clinical Research Centre, Ministry of Health Malaysia, Hospital Tuanku Fauziah, Kangar, Perlis, Malaysia.
- 2. Department of Pharmacy, Hospital Sultanah Bahiyah, Ministry of Health Malaysia, Alor Setar, Kedah, Malaysia.
Description
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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JPC_Granulomatosis.pdf
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