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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.
  • Carpenter K; Department of Internal Medicine, Saint Louis University, Saint Louis, MO, United States.
  • Etemady-Deylamy A; Department of Internal Medicine, Saint Louis University, Saint Louis, MO, United States.
  • Costello V; Department of Internal Medicine, Saint Louis University, Saint Louis, MO, United States.
  • Khasawneh M; Department of Internal Medicine, Saint Louis University, Saint Louis, MO, United States.
  • Chamberland R; SSM Saint Louis Network Microbiology, Saint Louis, MO, United States.
  • Tian K; Department of Pathology, Saint Louis University, Saint Louis, MO, United States.
  • Donlin M; Department of Internal Medicine, Saint Louis University, Saint Louis, MO, United States.
  • Moreira-Walsh B; Department of Molecular Microbiology and Immunology, Saint Louis University, Saint Louis, MO, United States.
  • Reisenbichler E; Department of Molecular Microbiology and Immunology, Saint Louis University, Saint Louis, MO, United States.
  • Abate G; Department of Pathology, Saint Louis University, Saint Louis, MO, United States.
Front Med (Lausanne) ; 9: 942751, 2022.
Article in English | MEDLINE | ID: covidwho-2065575
ABSTRACT
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.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Case report / Cohort study / Prognostic study / Reviews Language: English Journal: Front Med (Lausanne) Year: 2022 Document Type: Article Affiliation country: Fmed.2022.942751

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Case report / Cohort study / Prognostic study / Reviews Language: English Journal: Front Med (Lausanne) Year: 2022 Document Type: Article Affiliation country: Fmed.2022.942751