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[Three sisters of pulmonary Mycobacterium avium complex disease]
Tetsuro Inoue1, Eisaku Tanaka, Minoru Sakuramoto
1Department of Respiratory Medicine, TENRI Hospital.
Abstract:
We reported three sisters of pulmonary Mycobacterium avium complex (MAC) disease. The oldest sister was complaining of bloody sputum, and cultures were positive for M. avium. By monotherapy with clarithromycin, symptom and imaging findings had shown no progression for six years. The second sister was complaining of productive cough, and cultures were positive for M. intracellulare. Her symptom and imaging findings had shown no progression for seven years without any treatment. The third sister had rheumatoid arthritis and diabetes mellitus, and cultures were positive for M. intracellulare. Although she received chemotherapy with rifampicin, clarithromycin, ethambutol, and kanamycin, symptom and imaging findings had progressed gradually. She died of respiratory failure four years later. Autopsy findings revealed no disseminated MAC disease. The results which three cases showed different isolate patterns and clinical courses suggest the importance of underlying anti-mycobacterial immunological impairment and defects of local host defense rather than virulence of infected strains as the pathogenesis of pulmonary MAC disease.
Insights
Three sisters with pulmonary Mycobacterium avium complex (MAC) disease showed varied responses to infection. Underlying immune defects, not bacterial strain virulence, likely dictate disease progression in pulmonary MAC.
Area of Science:
- Pulmonary Medicine
- Infectious Diseases
- Immunology
Background:
- Pulmonary Mycobacterium avium complex (MAC) disease is a significant global health concern.
- Understanding the pathogenesis of pulmonary MAC is crucial for effective treatment strategies.
Observation:
- Three sisters presented with pulmonary MAC disease, each infected with different MAC species (M. avium and M. intracellulare).
- The oldest sister responded well to clarithromycin monotherapy, showing no progression for six years.
- The second sister showed no disease progression for seven years without treatment.
- The third sister, with comorbidities, experienced disease progression despite multi-drug chemotherapy and ultimately succumbed to respiratory failure.
Findings:
- Clinical courses and isolate patterns varied significantly among the sisters.
- Disease progression appeared independent of the specific MAC isolate or treatment regimen in one case.
- Autopsy revealed no disseminated MAC disease, suggesting localized pulmonary infection.
Implications:
- The findings highlight the critical role of host immune status in pulmonary MAC pathogenesis.
- Underlying anti-mycobacterial immunological impairment and local host defense defects are likely more important than bacterial strain virulence.
- Further research into host-pathogen interactions and immune responses is warranted for improved therapeutic approaches.
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