Related Experiment Video
Updated: Sep 10, 2025

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Non-resolving pneumonia revealing ANCA vasculitis.
Ashwin Karnan1, Babaji Ghewade2, Ulhas Jadhav2
1Respiratory Medicine, Datta Meghe Institute of Higher Education & Research (Deemed to be University), Wardha, Maharashtra, India ashwin2700@gmail.com.
This case highlights granulomatosis with polyangiitis, a rare condition that can mimic pneumonia. Early diagnosis and treatment with glucocorticoids led to significant patient recovery.
Area of Science:
- Internal Medicine
- Rheumatology
- Pulmonology
Background:
- Pneumonia can present with non-resolving symptoms, necessitating a broader differential diagnosis.
- Granulomatosis with polyangiitis (GPA) is a rare systemic vasculitis that can affect multiple organs, including the lungs.
- Pulmonary infarction, a potential complication of thromboembolism, can mimic infectious pneumonia.
Purpose of the Study:
- To present a case of granulomatosis with polyangiitis (GPA) initially misdiagnosed as community-acquired pneumonia.
- To emphasize the importance of considering rare diagnoses and diagnostic clues in non-resolving pneumonia.
- To illustrate the effective management of GPA with oral glucocorticoids.
Main Methods:
- A comprehensive diagnostic workup was performed for a patient with persistent pneumonia symptoms.
- Diagnostic investigations included laboratory tests (anemia, neutrophilic leukocytosis, elevated D-dimer and CRP, positive c-ANCA) and radiological imaging.
- The patient was treated with oral glucocorticoids, and clinical, biochemical, and radiological outcomes were monitored.
Main Results:
- The patient, a farmer with diabetes and heart failure, presented with a 1-month history of non-resolving pneumonia.
- Diagnostic workup revealed granulomatosis with polyangiitis (GPA), characterized by anemia, neutrophilic leukocytosis, acute kidney injury, elevated inflammatory markers, and a positive cytoplasmic anti-neutrophil cytoplasmic antibody (c-ANCA).
- Following a 4-week course of oral glucocorticoids, the patient demonstrated significant clinical, biochemical, and radiological improvement.
Conclusions:
- Granulomatosis with polyangiitis (GPA) can present atypically, mimicking common conditions like pneumonia.
- Pulmonary infarction, a sign of embolism, should be considered in patients with risk factors and may present as a Hampton's hump.
- This case underscores the critical role of recognizing rare disease presentations, utilizing diagnostic clues, and implementing appropriate management strategies for vasculitis.
Related Concept Videos
Pneumonia III: Complications and Assessment
Acute Pyelonephritis II: Diagnostic Studies and Management
Pneumonia II: Pathophysiology
Acute Pyelonephritis I: Introduction
Myocarditis II: Clinical Features and Diagnostic Tests
Pericarditis II: Clinical Features and Diagnostic Tests

