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Pulmonary mucormycosis associated with medical marijuana use

A 66-year-old man with diabetes presented to the hospital with a two-month history of dyspnea, cough, rust-colored sputum, night sweats and 20 pound weight loss. He had begun smoking medical marijuana 3 months earlier. CT of the chest showed multiple bilateral large ground glass opacities with surro...

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Detalles Bibliográficos
Autores principales: Stone, Taylor, Henkle, Joseph, Prakash, Vidhya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330507/
https://www.ncbi.nlm.nih.gov/pubmed/30671341
http://dx.doi.org/10.1016/j.rmcr.2019.01.008
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author Stone, Taylor
Henkle, Joseph
Prakash, Vidhya
author_facet Stone, Taylor
Henkle, Joseph
Prakash, Vidhya
author_sort Stone, Taylor
collection PubMed
description A 66-year-old man with diabetes presented to the hospital with a two-month history of dyspnea, cough, rust-colored sputum, night sweats and 20 pound weight loss. He had begun smoking medical marijuana 3 months earlier. CT of the chest showed multiple bilateral large ground glass opacities with surrounding consolidation. Infectious workup was negative. BAL was non-diagnostic. He was treated with broad spectrum antibiotics without improvement. VATS was performed and cultured lung tissue grew Rhizopus species. He was started on intravenous liposomal amphotericin B and micafungin and then transitioned to oral posaconazole after two weeks. Repeat CT two months later showed stable size of the cavities. One month later he died of massive pulmonary hemorrhage. Here we document what we believe is the first known case of pulmonary mucormycosis associated with medical marijuana use.
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spelling pubmed-63305072019-01-22 Pulmonary mucormycosis associated with medical marijuana use Stone, Taylor Henkle, Joseph Prakash, Vidhya Respir Med Case Rep Case Report A 66-year-old man with diabetes presented to the hospital with a two-month history of dyspnea, cough, rust-colored sputum, night sweats and 20 pound weight loss. He had begun smoking medical marijuana 3 months earlier. CT of the chest showed multiple bilateral large ground glass opacities with surrounding consolidation. Infectious workup was negative. BAL was non-diagnostic. He was treated with broad spectrum antibiotics without improvement. VATS was performed and cultured lung tissue grew Rhizopus species. He was started on intravenous liposomal amphotericin B and micafungin and then transitioned to oral posaconazole after two weeks. Repeat CT two months later showed stable size of the cavities. One month later he died of massive pulmonary hemorrhage. Here we document what we believe is the first known case of pulmonary mucormycosis associated with medical marijuana use. Elsevier 2019-01-09 /pmc/articles/PMC6330507/ /pubmed/30671341 http://dx.doi.org/10.1016/j.rmcr.2019.01.008 Text en © 2019 The Authors. Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Stone, Taylor
Henkle, Joseph
Prakash, Vidhya
Pulmonary mucormycosis associated with medical marijuana use
title Pulmonary mucormycosis associated with medical marijuana use
title_full Pulmonary mucormycosis associated with medical marijuana use
title_fullStr Pulmonary mucormycosis associated with medical marijuana use
title_full_unstemmed Pulmonary mucormycosis associated with medical marijuana use
title_short Pulmonary mucormycosis associated with medical marijuana use
title_sort pulmonary mucormycosis associated with medical marijuana use
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330507/
https://www.ncbi.nlm.nih.gov/pubmed/30671341
http://dx.doi.org/10.1016/j.rmcr.2019.01.008
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