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Mycobacterium chimaera Disseminated Infection
Ruben de Melo Carvalho1, Ana Luisa Nunes2, Rosa Sa1
1Servico de Doencas Infeciosas do Centro Hospitalar Universitario de Coimbra, Coimbra, Portugal.
Journal of Medical Cases
|August 26, 2021
Summary
Disseminated Mycobacterium chimaera infection in an immunocompromised patient was successfully treated with a four-drug regimen. Molecular genetic testing confirmed the species, guiding therapy despite complications.
Area of Science:
- Infectious Diseases
- Medical Microbiology
- Immunocompromised Hosts
Background:
- Nontuberculous mycobacterial (NTM) diseases are increasing, necessitating accurate species identification for effective treatment.
- Molecular microbiology techniques enhance understanding of NTM pathogenicity and treatment responses.
- Immunocompromised patients, particularly those with hematologic malignancies, are at higher risk for disseminated NTM infections.
Observation:
- A 57-year-old man with B-cell lymphoma developed fever, night sweats, and asthenia, progressing to pneumonia, anemia, and hepatosplenomegaly.
- Blood, bronchoalveolar lavage, and bone marrow cultures revealed disseminated *Mycobacterium avium-intracellulare* complex infection.
- Initial empirical antibiotics were ineffective, requiring a multi-drug regimen.
Findings:
- Species identification using the GenoType NTM-DR test confirmed *Mycobacterium chimaera* (MC).
- A four-drug regimen (clarithromycin, rifabutin, ethambutol, and moxifloxacin) was effective, with slow but gradual clinical improvement.
- Treatment led to negative cultures after 4 months and was continued for 12 months, demonstrating successful infection control.
Implications:
- This case highlights the successful use of molecular diagnostics for rapid and accurate identification of MC.
- A four-drug regimen can effectively treat severe, disseminated MC infections in immunocompromised individuals.
- Despite successful infection treatment, underlying conditions like B-cell lymphoma relapse can impact patient outcomes.
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