Systemic p-ANCA vasculitis with fatal outcome, arising in the setting of methimazole use

Sean Hacking1, Nupur N Uppal2, Neelofar Khan2

  • 1Department of Pathology and Laboratory Medicine and.

Insights

Methimazole, a drug used for hyperthyroidism, can rarely cause severe antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV). This case highlights a fatal outcome, emphasizing the need for awareness of this rare but serious adverse drug reaction.

Area of Science:

  • Nephrology
  • Rheumatology
  • Pathology

Background:

  • Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a group of autoimmune diseases characterized by inflammation of small blood vessels.
  • Drug-induced AAV is a known complication of several medications, but methimazole is less commonly associated.

Observation:

  • A 64-year-old woman presented with abdominal pain and colitis, progressing to hematuria, renal failure, and hemoptysis.
  • Serologic tests revealed positive antinuclear antibody (ANA), perinuclear-antineutrophilic cytoplasm antibodies (p-ANCA), and antimyeloperoxidase antibodies.
  • Autopsy confirmed widespread necrotizing vasculitis and crescentic glomerulonephritis, along with pulmonary alveolar hemorrhage.

Findings:

  • The patient's condition rapidly deteriorated, leading to pulselessness and expiration.
  • Histopathology revealed severe systemic vasculitis consistent with AAV.
  • Methimazole was identified as the likely causative agent, despite its rare association with AAV.

Implications:

  • This case underscores the potential for methimazole to induce severe and fatal ANCA-associated vasculitis.
  • Increased clinical suspicion and awareness are crucial for early diagnosis and management of methimazole-induced AAV.
  • Further research into the mechanisms and risk factors for methimazole-induced AAV is warranted.

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