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Recurrent Multifocal Mycoplasma orale Infection in an Immunocompromised Patient: A Case Report and Review

A young woman with mixed connective tissue disease complicated by erosive arthritis, secondary hypogammaglobulinemia due to rituximab, and a history of many infectious complications developed multiple nonhealing wounds, polyarticular joint pain, and leukocytosis. Radiographic studies demonstrated mu...

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Detalles Bibliográficos
Autores principales: Ketchersid, Jeffrey, Scott, Jake, Lew, Thomas, Banaei, Niaz, Kappagoda, Shanthi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7436331/
https://www.ncbi.nlm.nih.gov/pubmed/32850161
http://dx.doi.org/10.1155/2020/8852115
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author Ketchersid, Jeffrey
Scott, Jake
Lew, Thomas
Banaei, Niaz
Kappagoda, Shanthi
author_facet Ketchersid, Jeffrey
Scott, Jake
Lew, Thomas
Banaei, Niaz
Kappagoda, Shanthi
author_sort Ketchersid, Jeffrey
collection PubMed
description A young woman with mixed connective tissue disease complicated by erosive arthritis, secondary hypogammaglobulinemia due to rituximab, and a history of many infectious complications developed multiple nonhealing wounds, polyarticular joint pain, and leukocytosis. Radiographic studies demonstrated multiple scattered areas of osteomyelitis and complex abscesses. Purulent fluid drained from multiple sites did not yield a microbiologic diagnosis by standard culture technique, but Mycoplasma orale was ultimately identified using 16 S ribosomal RNA gene amplification and sequencing. We describe this unique case and review the literature.
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spelling pubmed-74363312020-08-25 Recurrent Multifocal Mycoplasma orale Infection in an Immunocompromised Patient: A Case Report and Review Ketchersid, Jeffrey Scott, Jake Lew, Thomas Banaei, Niaz Kappagoda, Shanthi Case Rep Infect Dis Case Report A young woman with mixed connective tissue disease complicated by erosive arthritis, secondary hypogammaglobulinemia due to rituximab, and a history of many infectious complications developed multiple nonhealing wounds, polyarticular joint pain, and leukocytosis. Radiographic studies demonstrated multiple scattered areas of osteomyelitis and complex abscesses. Purulent fluid drained from multiple sites did not yield a microbiologic diagnosis by standard culture technique, but Mycoplasma orale was ultimately identified using 16 S ribosomal RNA gene amplification and sequencing. We describe this unique case and review the literature. Hindawi 2020-08-09 /pmc/articles/PMC7436331/ /pubmed/32850161 http://dx.doi.org/10.1155/2020/8852115 Text en Copyright © 2020 Jeffrey Ketchersid et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ketchersid, Jeffrey
Scott, Jake
Lew, Thomas
Banaei, Niaz
Kappagoda, Shanthi
Recurrent Multifocal Mycoplasma orale Infection in an Immunocompromised Patient: A Case Report and Review
title Recurrent Multifocal Mycoplasma orale Infection in an Immunocompromised Patient: A Case Report and Review
title_full Recurrent Multifocal Mycoplasma orale Infection in an Immunocompromised Patient: A Case Report and Review
title_fullStr Recurrent Multifocal Mycoplasma orale Infection in an Immunocompromised Patient: A Case Report and Review
title_full_unstemmed Recurrent Multifocal Mycoplasma orale Infection in an Immunocompromised Patient: A Case Report and Review
title_short Recurrent Multifocal Mycoplasma orale Infection in an Immunocompromised Patient: A Case Report and Review
title_sort recurrent multifocal mycoplasma orale infection in an immunocompromised patient: a case report and review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7436331/
https://www.ncbi.nlm.nih.gov/pubmed/32850161
http://dx.doi.org/10.1155/2020/8852115
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