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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.
Abstract:
Here we report a fatal case of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) due to methimazole use in a 64-year-old woman. She was initially hospitalized for abdominal pain and possible colitis, and subsequently developed hematuria, renal failure, and hemoptysis. The serologic work-up revealed positive antinuclear antibody (ANA) and perinuclear-antineutrophilic cytoplasm antibodies (p-ANCA), with positive antimyeloperoxidase. Three weeks following admission, the patient was found to be pulseless, and expired. At autopsy, microscopic review included widespread transmural necrotizing vasculitis and crescentic glomerulonephritis in the kidney, and diffuse pulmonary alveolar hemorrhage; focal coronary artery intimal vasculitis and necrotizing pericarditis were also noted. Several drugs have been associated with the development of ANCA-positive diseases, including propylthiouracil, hydralazine, allopurinol, penicillamine, and levamisole in cocaine. Association of ANCA vasculitis with methimazole exposure is less known, and severe presentation with fatal outcome, as seen in our patient, is exceedingly rare. We reviewed clinical and histopathologic features of drug-induced ANCA vasculitis associated with methimazole to raise awareness of this potentially life-threatening complication associated with this agent.
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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