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Cryptococcal chest wall mass and rib osteomyelitis associated with the use of fingolimod: A case report and literature review
Being introduced in 2010, fingolimod was among the first oral therapies for relapsing multiple sclerosis (MS). Since that time, postmarketing surveillance has noted several case reports of various cryptococcal infections associated with fingolimod use. To date, approximately 15 such case reports hav...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9491343/ https://www.ncbi.nlm.nih.gov/pubmed/36160166 http://dx.doi.org/10.3389/fmed.2022.942751 |
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author | Carpenter, Kent Etemady-Deylamy, Ali Costello, Victoria Khasawneh, Mohammad Chamberland, Robin Tian, Katherine Donlin, Maureen Moreira-Walsh, Brenda Reisenbichler, Emily Abate, Getahun |
author_facet | Carpenter, Kent Etemady-Deylamy, Ali Costello, Victoria Khasawneh, Mohammad Chamberland, Robin Tian, Katherine Donlin, Maureen Moreira-Walsh, Brenda Reisenbichler, Emily Abate, Getahun |
author_sort | Carpenter, Kent |
collection | PubMed |
description | Being introduced in 2010, fingolimod was among the first oral therapies for relapsing multiple sclerosis (MS). Since that time, postmarketing surveillance has noted several case reports of various cryptococcal infections associated with fingolimod use. To date, approximately 15 such case reports have been published. We present the first and unique case of cryptococcal chest wall mass and rib osteomyelitis associated with fingolimod use. The patient presented with left-side chest pain and was found to have a lower left chest wall mass. Computerized tomography (CT) showed chest wall mass with the destruction of left 7th rib. Aspirate from the mass grew Cryptococcus neoformans. The isolate was serotype A. Fingolimod was stopped. The patient received liposomal amphotericin B for 2 weeks and started on fluconazole with a plan to continue for 6–12 months. The follow-up CT in 6 weeks showed a marked decrease in the size of the chest wall mass. In conclusion, our case highlights the atypical and aggressive form of cryptococcal infection possibly related to immunosuppression from fingolimod use. |
format | Online Article Text |
id | pubmed-9491343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94913432022-09-22 Cryptococcal chest wall mass and rib osteomyelitis associated with the use of fingolimod: A case report and literature review Carpenter, Kent Etemady-Deylamy, Ali Costello, Victoria Khasawneh, Mohammad Chamberland, Robin Tian, Katherine Donlin, Maureen Moreira-Walsh, Brenda Reisenbichler, Emily Abate, Getahun Front Med (Lausanne) Medicine Being introduced in 2010, fingolimod was among the first oral therapies for relapsing multiple sclerosis (MS). Since that time, postmarketing surveillance has noted several case reports of various cryptococcal infections associated with fingolimod use. To date, approximately 15 such case reports have been published. We present the first and unique case of cryptococcal chest wall mass and rib osteomyelitis associated with fingolimod use. The patient presented with left-side chest pain and was found to have a lower left chest wall mass. Computerized tomography (CT) showed chest wall mass with the destruction of left 7th rib. Aspirate from the mass grew Cryptococcus neoformans. The isolate was serotype A. Fingolimod was stopped. The patient received liposomal amphotericin B for 2 weeks and started on fluconazole with a plan to continue for 6–12 months. The follow-up CT in 6 weeks showed a marked decrease in the size of the chest wall mass. In conclusion, our case highlights the atypical and aggressive form of cryptococcal infection possibly related to immunosuppression from fingolimod use. Frontiers Media S.A. 2022-09-07 /pmc/articles/PMC9491343/ /pubmed/36160166 http://dx.doi.org/10.3389/fmed.2022.942751 Text en Copyright © 2022 Carpenter, Etemady-Deylamy, Costello, Khasawneh, Chamberland, Tian, Donlin, Moreira-Walsh, Reisenbichler and Abate. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Carpenter, Kent Etemady-Deylamy, Ali Costello, Victoria Khasawneh, Mohammad Chamberland, Robin Tian, Katherine Donlin, Maureen Moreira-Walsh, Brenda Reisenbichler, Emily Abate, Getahun Cryptococcal chest wall mass and rib osteomyelitis associated with the use of fingolimod: A case report and literature review |
title | Cryptococcal chest wall mass and rib osteomyelitis associated with the use of fingolimod: A case report and literature review |
title_full | Cryptococcal chest wall mass and rib osteomyelitis associated with the use of fingolimod: A case report and literature review |
title_fullStr | Cryptococcal chest wall mass and rib osteomyelitis associated with the use of fingolimod: A case report and literature review |
title_full_unstemmed | Cryptococcal chest wall mass and rib osteomyelitis associated with the use of fingolimod: A case report and literature review |
title_short | Cryptococcal chest wall mass and rib osteomyelitis associated with the use of fingolimod: A case report and literature review |
title_sort | cryptococcal chest wall mass and rib osteomyelitis associated with the use of fingolimod: a case report and literature review |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9491343/ https://www.ncbi.nlm.nih.gov/pubmed/36160166 http://dx.doi.org/10.3389/fmed.2022.942751 |
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