Granulomatosis With Polyangiitis Misdiagnosed as Tuberculosis: A Case Report

José Diogo Martins1, Catarina Soares2, Cátia Barreiros1

  • 1Internal Medicine, Unidade Local de Saúde do Alto Minho, Viana do Castelo, PRT.

Cureus
|November 19, 2024
PubMed

Insights

Granulomatosis with polyangiitis (GPA) is a rare autoimmune vasculitis affecting the lungs and kidneys. Early diagnosis is crucial, as this case highlights potential misdiagnosis with pulmonary tuberculosis due to similar imaging findings.

Area of Science:

  • Rheumatology
  • Pulmonology
  • Nephrology

Background:

  • Granulomatosis with polyangiitis (GPA), previously Wegener's granulomatosis, is a rare autoimmune disease.
  • Characterized by necrotizing vasculitis affecting small to medium-sized vessels.
  • Primarily impacts the lungs, kidneys, and upper respiratory tract.

Observation:

  • A 48-year-old male presented with respiratory symptoms suggestive of GPA.
  • The patient had primary pulmonary and articular involvement.
  • Imaging revealed cavitary lesions, leading to an initial misdiagnosis of pulmonary tuberculosis.

Findings:

  • The case underscores the diagnostic challenges in GPA, particularly when presenting with pulmonary involvement.
  • Cavitary lung lesions can mimic other conditions like tuberculosis.
  • Timely and accurate diagnosis is essential for effective management.

Implications:

  • Highlights the importance of considering GPA in patients with unexplained respiratory and articular symptoms.
  • Emphasizes the need for comprehensive diagnostic workups to differentiate GPA from infectious diseases.
  • Early intervention in GPA can significantly improve patient outcomes and prevent organ damage.

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