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Isolated bilateral renal mucormycosis in apparently immunocompetent patients—a case series from India and review of the literature
BACKGROUND: Isolated renal mucormycosis (IRM) is a potentially fatal disease affecting immunocompromised hosts. IRM affecting apparently immunocompetent patients is rare, with few previous reports, mostly from India. We describe 10 cases of bilateral IRM with no underlying risk factors. METHODS: We...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275442/ https://www.ncbi.nlm.nih.gov/pubmed/30524710 http://dx.doi.org/10.1093/ckj/sfy034 |
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author | Bhadauria, Dharmendra Etta, Praveen Chelappan, Anand Gurjar, Mohan Kaul, Anupma Sharma, Raj Kumar Gupta, Amit Prasad, Narayan Marak, Rungmei S Jain, Manoj Srivastava, Aneesh Lal, Hira |
author_facet | Bhadauria, Dharmendra Etta, Praveen Chelappan, Anand Gurjar, Mohan Kaul, Anupma Sharma, Raj Kumar Gupta, Amit Prasad, Narayan Marak, Rungmei S Jain, Manoj Srivastava, Aneesh Lal, Hira |
author_sort | Bhadauria, Dharmendra |
collection | PubMed |
description | BACKGROUND: Isolated renal mucormycosis (IRM) is a potentially fatal disease affecting immunocompromised hosts. IRM affecting apparently immunocompetent patients is rare, with few previous reports, mostly from India. We describe 10 cases of bilateral IRM with no underlying risk factors. METHODS: We performed a retrospective analysis of cases of IRM from our hospital information system admitted between 2009 and 2016. We analyzed the data of this cohort of IRM, including epidemiological characteristics, clinical presentation, diagnostic procedures, treatment details and outcome. RESULTS: In all, 10 cases of bilateral IRM were identified. All of them were males with a mean age of 24.7 years (range 10–42). Most patients were initially managed as acute bacterial pyelonephritis with acute kidney injury. A total of eight patients were diagnosed antemortem. Diagnostic clues include sepsis not controlled with broad-spectrum antibiotics and enlarged kidneys with or without hypodensities on ultrasound/computed tomography imaging. Three patients also gave a specific history of passing white flakes in their urine. Eight patients received specific antifungal therapy with amphotericin B with or without posaconazole. Three patients in whom the disease was apparently confined to the pelvicalyceal system underwent local irrigation with Amp-B. One patient underwent bilateral nephrectomy. Four patients succumbed to the disease while five patients were successfully treated. One patient was discharged against medical advice. CONCLUSIONS: IRM is a rare, life-threatening disease associated with high mortality even in immunocompetent individuals. Typical clinical and radiological findings and a high index of suspicion may help in early diagnosis, but definitive diagnosis requires histopathological and/or microbiological confirmation. Early and rapid diagnosis along with aggressive multidisciplinary management including initiation of specific antifungal therapy with or without surgical debridement is vital for a successful outcome. |
format | Online Article Text |
id | pubmed-6275442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62754422018-12-06 Isolated bilateral renal mucormycosis in apparently immunocompetent patients—a case series from India and review of the literature Bhadauria, Dharmendra Etta, Praveen Chelappan, Anand Gurjar, Mohan Kaul, Anupma Sharma, Raj Kumar Gupta, Amit Prasad, Narayan Marak, Rungmei S Jain, Manoj Srivastava, Aneesh Lal, Hira Clin Kidney J Infection BACKGROUND: Isolated renal mucormycosis (IRM) is a potentially fatal disease affecting immunocompromised hosts. IRM affecting apparently immunocompetent patients is rare, with few previous reports, mostly from India. We describe 10 cases of bilateral IRM with no underlying risk factors. METHODS: We performed a retrospective analysis of cases of IRM from our hospital information system admitted between 2009 and 2016. We analyzed the data of this cohort of IRM, including epidemiological characteristics, clinical presentation, diagnostic procedures, treatment details and outcome. RESULTS: In all, 10 cases of bilateral IRM were identified. All of them were males with a mean age of 24.7 years (range 10–42). Most patients were initially managed as acute bacterial pyelonephritis with acute kidney injury. A total of eight patients were diagnosed antemortem. Diagnostic clues include sepsis not controlled with broad-spectrum antibiotics and enlarged kidneys with or without hypodensities on ultrasound/computed tomography imaging. Three patients also gave a specific history of passing white flakes in their urine. Eight patients received specific antifungal therapy with amphotericin B with or without posaconazole. Three patients in whom the disease was apparently confined to the pelvicalyceal system underwent local irrigation with Amp-B. One patient underwent bilateral nephrectomy. Four patients succumbed to the disease while five patients were successfully treated. One patient was discharged against medical advice. CONCLUSIONS: IRM is a rare, life-threatening disease associated with high mortality even in immunocompetent individuals. Typical clinical and radiological findings and a high index of suspicion may help in early diagnosis, but definitive diagnosis requires histopathological and/or microbiological confirmation. Early and rapid diagnosis along with aggressive multidisciplinary management including initiation of specific antifungal therapy with or without surgical debridement is vital for a successful outcome. Oxford University Press 2018-12 2018-06-02 /pmc/articles/PMC6275442/ /pubmed/30524710 http://dx.doi.org/10.1093/ckj/sfy034 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of ERA-EDTA. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Infection Bhadauria, Dharmendra Etta, Praveen Chelappan, Anand Gurjar, Mohan Kaul, Anupma Sharma, Raj Kumar Gupta, Amit Prasad, Narayan Marak, Rungmei S Jain, Manoj Srivastava, Aneesh Lal, Hira Isolated bilateral renal mucormycosis in apparently immunocompetent patients—a case series from India and review of the literature |
title | Isolated bilateral renal mucormycosis in apparently immunocompetent patients—a case series from India and review of the literature |
title_full | Isolated bilateral renal mucormycosis in apparently immunocompetent patients—a case series from India and review of the literature |
title_fullStr | Isolated bilateral renal mucormycosis in apparently immunocompetent patients—a case series from India and review of the literature |
title_full_unstemmed | Isolated bilateral renal mucormycosis in apparently immunocompetent patients—a case series from India and review of the literature |
title_short | Isolated bilateral renal mucormycosis in apparently immunocompetent patients—a case series from India and review of the literature |
title_sort | isolated bilateral renal mucormycosis in apparently immunocompetent patients—a case series from india and review of the literature |
topic | Infection |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275442/ https://www.ncbi.nlm.nih.gov/pubmed/30524710 http://dx.doi.org/10.1093/ckj/sfy034 |
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