Cargando…
Disseminated Mycobacterium genavense in the immunocompromised: A Case Series at Mayo Clinic Rochester
BACKGROUND: Mycobacterium genavense can cause serious disease in the immunocompromised. We report our experience with this uncommon infection. METHODS: Retrospective review of M. genavense infection at Mayo Clinic (2010–2017). RESULTS: Three patients were diagnosed with M. genavense from 2010 to 201...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630744/ http://dx.doi.org/10.1093/ofid/ofx163.1796 |
_version_ | 1783269282195439616 |
---|---|
author | Mahmood, Maryam Ajmal, Saira Marcelin, Jasmine R Saleh, Omar Abu |
author_facet | Mahmood, Maryam Ajmal, Saira Marcelin, Jasmine R Saleh, Omar Abu |
author_sort | Mahmood, Maryam |
collection | PubMed |
description | BACKGROUND: Mycobacterium genavense can cause serious disease in the immunocompromised. We report our experience with this uncommon infection. METHODS: Retrospective review of M. genavense infection at Mayo Clinic (2010–2017). RESULTS: Three patients were diagnosed with M. genavense from 2010 to 2017 (Table 1). Lymph node biopsy noted non-necrotizing granulomatous inflammation with AFB in 2 patients. Delayed growth in culture was noted after at least 6 weeks incubation. All patients were started on mycobacterial therapy; no isolate grew sufficiently for drug susceptibility testing. CONCLUSION: M. genavense is an environmental mycobacteria, it rarely causes infection in non-HIV hosts. Our cases involved advanced HIV, solid organ transplant and idiopathic CD4 lymphopenia. Presentation with GI and systemic symptoms is common, pulmonary and cutaneous less so. Growth in culture requires prolonged incubation (8–12 weeks) in broth media with Mycobactin J supplementation. Positive pathological examination for AFB organisms, negative probes for MTB or MAC combined with persistently negative cultures, should raise the suspicion for this organism in the right clinical setting. It is generally susceptible to rifamycins, fluoroquinolones and macrolides; resistant to isoniazid and sometimes pyrazinamide. Immunosuppression should be reduced if possible to speed recovery. Duration of therapy is usually at least 12 months for disseminated disease, depending on response and immunosuppression. DISCLOSURES: All authors: No reported disclosures. |
format | Online Article Text |
id | pubmed-5630744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56307442017-11-07 Disseminated Mycobacterium genavense in the immunocompromised: A Case Series at Mayo Clinic Rochester Mahmood, Maryam Ajmal, Saira Marcelin, Jasmine R Saleh, Omar Abu Open Forum Infect Dis Abstracts BACKGROUND: Mycobacterium genavense can cause serious disease in the immunocompromised. We report our experience with this uncommon infection. METHODS: Retrospective review of M. genavense infection at Mayo Clinic (2010–2017). RESULTS: Three patients were diagnosed with M. genavense from 2010 to 2017 (Table 1). Lymph node biopsy noted non-necrotizing granulomatous inflammation with AFB in 2 patients. Delayed growth in culture was noted after at least 6 weeks incubation. All patients were started on mycobacterial therapy; no isolate grew sufficiently for drug susceptibility testing. CONCLUSION: M. genavense is an environmental mycobacteria, it rarely causes infection in non-HIV hosts. Our cases involved advanced HIV, solid organ transplant and idiopathic CD4 lymphopenia. Presentation with GI and systemic symptoms is common, pulmonary and cutaneous less so. Growth in culture requires prolonged incubation (8–12 weeks) in broth media with Mycobactin J supplementation. Positive pathological examination for AFB organisms, negative probes for MTB or MAC combined with persistently negative cultures, should raise the suspicion for this organism in the right clinical setting. It is generally susceptible to rifamycins, fluoroquinolones and macrolides; resistant to isoniazid and sometimes pyrazinamide. Immunosuppression should be reduced if possible to speed recovery. Duration of therapy is usually at least 12 months for disseminated disease, depending on response and immunosuppression. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2017-10-04 /pmc/articles/PMC5630744/ http://dx.doi.org/10.1093/ofid/ofx163.1796 Text en © The Author 2017. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Mahmood, Maryam Ajmal, Saira Marcelin, Jasmine R Saleh, Omar Abu Disseminated Mycobacterium genavense in the immunocompromised: A Case Series at Mayo Clinic Rochester |
title | Disseminated Mycobacterium genavense in the immunocompromised: A Case Series at Mayo Clinic Rochester |
title_full | Disseminated Mycobacterium genavense in the immunocompromised: A Case Series at Mayo Clinic Rochester |
title_fullStr | Disseminated Mycobacterium genavense in the immunocompromised: A Case Series at Mayo Clinic Rochester |
title_full_unstemmed | Disseminated Mycobacterium genavense in the immunocompromised: A Case Series at Mayo Clinic Rochester |
title_short | Disseminated Mycobacterium genavense in the immunocompromised: A Case Series at Mayo Clinic Rochester |
title_sort | disseminated mycobacterium genavense in the immunocompromised: a case series at mayo clinic rochester |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630744/ http://dx.doi.org/10.1093/ofid/ofx163.1796 |
work_keys_str_mv | AT mahmoodmaryam disseminatedmycobacteriumgenavenseintheimmunocompromisedacaseseriesatmayoclinicrochester AT ajmalsaira disseminatedmycobacteriumgenavenseintheimmunocompromisedacaseseriesatmayoclinicrochester AT marcelinjasminer disseminatedmycobacteriumgenavenseintheimmunocompromisedacaseseriesatmayoclinicrochester AT salehomarabu disseminatedmycobacteriumgenavenseintheimmunocompromisedacaseseriesatmayoclinicrochester |