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An indolent case of isolated cerebral mucormycosis: an uncommon presentation
INTRODUCTION: This case is a presentation of isolated central nervous system (CNS) Mucormycosis in an immunocompetent patient. This case is unique in its demonstration of isolated CNS involvement while lacking clear evidence elucidating an entry point. CASE PRESENTATION: The patient is a 36-year-old...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Microbiology Society
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481736/ https://www.ncbi.nlm.nih.gov/pubmed/32974538 http://dx.doi.org/10.1099/acmi.0.000023 |
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author | Montgomery, David J. Goldstein, Randi S. Douse, Dontre' M. Tuitt, Jerome Sinnott, Michael |
author_facet | Montgomery, David J. Goldstein, Randi S. Douse, Dontre' M. Tuitt, Jerome Sinnott, Michael |
author_sort | Montgomery, David J. |
collection | PubMed |
description | INTRODUCTION: This case is a presentation of isolated central nervous system (CNS) Mucormycosis in an immunocompetent patient. This case is unique in its demonstration of isolated CNS involvement while lacking clear evidence elucidating an entry point. CASE PRESENTATION: The patient is a 36-year-old man without a pertinent past medical history, who initially presented with altered mental status and a 5-day history of progressively slurred speech. His social history is significant for intravenous drug use and outdoor pest control work. The patient’s head computed tomography (CT) scan without contrast demonstrated the presence of possible bilateral infarcts or masses involving the basal ganglia and periventricular white matter. The patient then progressed to facial diplegia with new onset hemiplegia. High-dose steroids were initiated due to concern for neurosarcoidosis. A lumbar puncture was ordered due to minimal improvement and suggested an inflammatory process. A stereotactic brain biopsy was then performed, demonstrating non-caseating granulomatous inflammation with giant cells. Liposomal amphotericin B was added to cover possible fungal etiology. The pathology report was consistent with an isolated cerebral mucormycosis infection. The etiology remained elusive with clear paranasal sinuses and no cutaneous manifestations. Due to extensive gray matter involvement, the patient was not a candidate for surgery. CONCLUSION: This is a report of mucormycosis in a seemingly immunocompetent patient with either isolated CNS involvement or disseminated mucormycosis without an identifiable source. Although this patient did have two risk factors including intravenous drug use and outdoor working history, his lack of peripheral involvement demonstrates an uncommon presentation. |
format | Online Article Text |
id | pubmed-7481736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Microbiology Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-74817362020-09-23 An indolent case of isolated cerebral mucormycosis: an uncommon presentation Montgomery, David J. Goldstein, Randi S. Douse, Dontre' M. Tuitt, Jerome Sinnott, Michael Access Microbiol Case Report INTRODUCTION: This case is a presentation of isolated central nervous system (CNS) Mucormycosis in an immunocompetent patient. This case is unique in its demonstration of isolated CNS involvement while lacking clear evidence elucidating an entry point. CASE PRESENTATION: The patient is a 36-year-old man without a pertinent past medical history, who initially presented with altered mental status and a 5-day history of progressively slurred speech. His social history is significant for intravenous drug use and outdoor pest control work. The patient’s head computed tomography (CT) scan without contrast demonstrated the presence of possible bilateral infarcts or masses involving the basal ganglia and periventricular white matter. The patient then progressed to facial diplegia with new onset hemiplegia. High-dose steroids were initiated due to concern for neurosarcoidosis. A lumbar puncture was ordered due to minimal improvement and suggested an inflammatory process. A stereotactic brain biopsy was then performed, demonstrating non-caseating granulomatous inflammation with giant cells. Liposomal amphotericin B was added to cover possible fungal etiology. The pathology report was consistent with an isolated cerebral mucormycosis infection. The etiology remained elusive with clear paranasal sinuses and no cutaneous manifestations. Due to extensive gray matter involvement, the patient was not a candidate for surgery. CONCLUSION: This is a report of mucormycosis in a seemingly immunocompetent patient with either isolated CNS involvement or disseminated mucormycosis without an identifiable source. Although this patient did have two risk factors including intravenous drug use and outdoor working history, his lack of peripheral involvement demonstrates an uncommon presentation. Microbiology Society 2019-05-07 /pmc/articles/PMC7481736/ /pubmed/32974538 http://dx.doi.org/10.1099/acmi.0.000023 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License. |
spellingShingle | Case Report Montgomery, David J. Goldstein, Randi S. Douse, Dontre' M. Tuitt, Jerome Sinnott, Michael An indolent case of isolated cerebral mucormycosis: an uncommon presentation |
title | An indolent case of isolated cerebral mucormycosis: an uncommon presentation |
title_full | An indolent case of isolated cerebral mucormycosis: an uncommon presentation |
title_fullStr | An indolent case of isolated cerebral mucormycosis: an uncommon presentation |
title_full_unstemmed | An indolent case of isolated cerebral mucormycosis: an uncommon presentation |
title_short | An indolent case of isolated cerebral mucormycosis: an uncommon presentation |
title_sort | indolent case of isolated cerebral mucormycosis: an uncommon presentation |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481736/ https://www.ncbi.nlm.nih.gov/pubmed/32974538 http://dx.doi.org/10.1099/acmi.0.000023 |
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