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Microscopic Polyangiitis After Pulmonary Nontuberculous Mycobacterial Disease: A Case Report and Literature Review
Hidenori Takahashi1, Riho Nakagawa1, Mio Toyama-Kousaka1
1Department of Respiratory Medicine Tokyo Shinagawa Hospital Tokyo Japan.
Abstract:
Nontuberculous mycobacterial pulmonary disease (NTM-PD) is generally considered an infectious condition. Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis is a rare complication that may mimic infectious exacerbation. An 80-year-old Japanese woman with a history of NTM-PD complicated by bronchiectasis and Pseudomonas aeruginosa colonisation presented with fever and a productive cough. Despite treatment with broad-spectrum antibiotics, the signs of inflammation persisted and urinalysis showed haematuria, proteinuria and casts. The myeloperoxidase (MPO)-ANCA test was strongly positive (783 U/mL). After intravenous methylprednisolone, followed by oral prednisolone, renal biopsy demonstrated pauci-immune crescentic glomerulonephritis and nerve conduction studies suggested axonal-type multiple mononeuropathy. Rituximab was initiated 1 week later. The MPO-ANCA titre decreased from 783 to 160 U/mL, renal function remained stable and systemic inflammation improved, although the neuropathy persisted. Clinicians should consider ANCA-associated vasculitis in the differential diagnosis when organ-specific findings emerge during presumed infectious exacerbations of NTM-PD.
Insights
Nontuberculous mycobacterial pulmonary disease (NTM-PD) can rarely present with anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis. Early recognition and treatment of this rare complication are crucial for managing NTM-PD patients.
Area of Science:
- Pulmonology
- Rheumatology
- Nephrology
Background:
- Nontuberculous mycobacterial pulmonary disease (NTM-PD) is typically viewed as an infection.
- Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis is a rare condition that can mimic infectious exacerbations of NTM-PD.
Purpose of the Study:
- To highlight the importance of considering ANCA-associated vasculitis in patients with NTM-PD presenting with atypical symptoms.
- To describe a case of NTM-PD complicated by ANCA-associated vasculitis.
Main Methods:
- Case report of an 80-year-old Japanese woman with NTM-PD.
- Clinical presentation, laboratory findings (including MPO-ANCA test), renal biopsy, and nerve conduction studies were analyzed.
- Treatment response to immunosuppressive therapy (methylprednisolone, prednisolone, rituximab) was evaluated.
Main Results:
- The patient presented with NTM-PD, bronchiectasis, and Pseudomonas aeruginosa colonization, exhibiting persistent inflammation, hematuria, proteinuria, and casts despite antibiotic treatment.
- Myeloperoxidase (MPO)-ANCA test was strongly positive (783 U/mL).
- Treatment with methylprednisolone, prednisolone, and rituximab led to a decrease in MPO-ANCA titre, stable renal function, and improved systemic inflammation, though neuropathy persisted.
Conclusions:
- ANCA-associated vasculitis is a rare but important complication to consider in patients with NTM-PD experiencing organ-specific manifestations.
- Prompt diagnosis and immunosuppressive treatment can improve outcomes in NTM-PD patients with concurrent ANCA-associated vasculitis.
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