GRANULOMATOSIS WITH POLYANGIITIS: A CASE REPORT

• Published in: Journal of evolution of medical and dental sciences Vol. 4; no. 31; pp. 5397 - 5402
• Main Authors: Kumar, Allena Prem, Usharani, Namballa, Yellapu, Gayatri Devi, Rao, Gorantla Samba Siva, Naik, Banavath Durga Prasad
• Format: Journal Article
• Language: English
• Published: Akshantala Enterprises Private Limited 16.04.2015
• Subjects: Care and treatment; Case studies; Diagnosis; Wegener's granulomatosis
• ISSN: 2278-4748; 2278-4802
• DOI: 10.14260/jemds/2015/789

INTRODUCTION: Granulomatosis with polyangiitis (GPA) is an important form of AAV (ANCA associated vasculitis) syndrome. Being a multisystem disease, it can manifest in several combinations and can mimic an infection or malignancy. CASE PRESENTATION: A 55 years old man presented with cough, expectoration, haemoptysis, chronic otorrhoea and hearing loss. Imaging study suggested malignant mass lesion in right upper lobe with metastasis. HRCT of Temporal bones showed chronic sclerosing mastoiditis with bilateral CSOM. USG Abdomen and urine examination suggested acute glomerulonephritis. Trucut biopsy of lung showed granuloma and ANCA assays showed him C ANCA positive. Treatment with prednisolone and cyclophosphamide resulted in rapid resolution of symptoms and radiological clearance. CONCLUSION: Since GPA can effect almost any organ and a high degree of suspicion should be maintained in any multisystemic disease. Rapid work up with biopsy and ANCA Assay and early treatment with immunosuppressants will prevent irreversible organ damage. KEYWORDS: GPA (Granulomatosis palyangiitis), ANCA (Anti Neutrophilic Cytoplasmic Antibodies), chronic sclerosing mastoiditis.