ANCA-associated Leucocytoclastic Vasculitis presenting with Bronchiectasis, GI Involvement and Hypertensive Urgency: A Complex Case without Renal Involvement

Introduction: Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are autoimmune diseases characterized by inflammation of small to medium blood vessels. This case explores AAV pathophysiology, its link to bronchiectasis and leucocytoclasia, ANCA positivity, and current treatmen...

Full description

Saved in:
Bibliographic Details
Main Authors: N. M. M. Risly, I. K. Jayasinghe, N. Athauda, E. M. C. B. Ekanayake, S. Hettige, J. F. Sahana
Format: Article
Language:English
Published: The Kandy Society of Medicine 2024-12-01
Series:Sri Lanka Journal of Medicine
Subjects:
Online Access:https://account.sljm.sljol.info/index.php/sljo-j-sljm2/article/view/552
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Introduction: Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are autoimmune diseases characterized by inflammation of small to medium blood vessels. This case explores AAV pathophysiology, its link to bronchiectasis and leucocytoclasia, ANCA positivity, and current treatment guidelines. Case Presentation: A 48-year-old with abdominal pain, rash, hypertensive urgency, and respiratory symptoms was diagnosed with AAV, confirmed by skin biopsy and positive C-ANCA, stool occult blood with negative abdominal imaging along with bronchiectasis on HRCT. The patient initially failed to respond to broad-spectrum antibiotics but improved with high-dose corticosteroids. Conclusion: We highlight an atypical presentation of AAV, showing the importance of timely immunosuppressive therapy for favorable outcomes.
ISSN:2579-1990