Pancreatic Head Mass: A Rare Manifestation of Granulomatosis With Polyangiitis

Michael Castillo1, Adalberto Gonzalez1, Asad Ur Rahman2

  • 1Department of Internal Medicine, Cleveland Clinic Florida, Weston, FL.

ACG Case Reports Journal
|December 14, 2019
PubMed

Insights

Granulomatosis with polyangiitis can rarely cause pancreatic masses, mimicking cancer. Treatment with immunosuppression resolved the pancreatic mass in this rare case.

Area of Science:

  • Internal Medicine
  • Rheumatology
  • Gastroenterology

Background:

  • Granulomatosis with polyangiitis (GPA) is a rare systemic vasculitis.
  • GPA typically affects the respiratory tract and kidneys.
  • Pancreatic involvement in GPA is exceptionally rare.

Observation:

  • A 73-year-old male presented with fever and weight loss.
  • CT imaging revealed a pancreatic head mass and pulmonary nodules.
  • Differential diagnosis included pancreatic cancer and autoimmune processes.

Findings:

  • Diagnosis of GPA was confirmed by positive cytoplasmic antineutrophil cytoplasmic antibodies and lung biopsy.
  • The pancreatic mass resolved completely after immunosuppressive therapy.
  • This case highlights GPA as a rare cause of pancreatic masses.

Implications:

  • GPA should be considered in the differential diagnosis of pancreatic masses, especially with concurrent pulmonary findings.
  • Successful treatment of GPA can lead to resolution of pancreatic lesions.
  • Further research is needed to define optimal management strategies for GPA-associated pancreatic masses.

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