Why the study?
Granulomatosis with polyangiitis can mimic infection and malignancy, creating significant diagnostic challenges that impact timely treatment.
Case Report (n=1)
No
Highlights the diagnostic challenge of Granulomatosis with polyangiitis overlapping with infection and malignancy, and the importance of early immunosuppressive therapy.
Answers are grounded in this paper and cite their sources.
Case underscores GPA mimicry in infection-like presentations; leaves open need for prospective diagnostic algorithms.
Granulomatosis with polyangiitis (GPA) is an antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis that can mimic infection and malignancy, posing a significant diagnostic challenge. We report the case of a 39-year-old male smoker with a strong family history of lung cancer who presented with fever, weight loss, dyspnea, and hemoptysis. Initial evaluation supported infection, with sputum cultures positive for Pseudomonas aeruginosa and Haemophilus influenzae. Imaging later revealed pulmonary masses suspicious for malignancy. The patient subsequently deteriorated with massive hemoptysis and acute kidney injury, requiring ICU admission, mechanical ventilation, blood transfusion, and dialysis. Further investigations demonstrated proteinase 3-ANCA positivity and diffuse alveolar hemorrhage on bronchoalveolar lavage, confirming GPA. Treatment with pulse corticosteroids, IV cyclophosphamide, and plasma exchange resulted in marked clinical recovery. This case underscores the significant diagnostic challenge posed by the overlap between infection, malignancy, and ANCA-associated vasculitis, highlighting the importance of early recognition and timely initiation of immunosuppressive therapy.
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Saleh et al. (2026) conducted a case report in Granulomatosis with polyangiitis (n=1). Pulse corticosteroids, IV cyclophosphamide, and plasma exchange was evaluated on Clinical recovery.
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