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Potential pathogenicity of Inquilinus limosus in a pediatric patient with cystic fibrosis

PRESENTATION: Patient is a 6‐year‐old male with CF, MRSA colonization, and pancreatic insufficiency that presented with worsening ppFEV1 and systemic symptoms despite multiple interventions. BAL grew NTM, Stenotrophomonas maltophilia, and Inquilinus limosus, a rare organism found in patients with CF...

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Detalles Bibliográficos
Autores principales: Poore, T. Spencer, Virella‐Lowell, Isabel, Guimbellot, Jennifer S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219391/
https://www.ncbi.nlm.nih.gov/pubmed/29790674
http://dx.doi.org/10.1002/ppul.24043
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author Poore, T. Spencer
Virella‐Lowell, Isabel
Guimbellot, Jennifer S.
author_facet Poore, T. Spencer
Virella‐Lowell, Isabel
Guimbellot, Jennifer S.
author_sort Poore, T. Spencer
collection PubMed
description PRESENTATION: Patient is a 6‐year‐old male with CF, MRSA colonization, and pancreatic insufficiency that presented with worsening ppFEV1 and systemic symptoms despite multiple interventions. BAL grew NTM, Stenotrophomonas maltophilia, and Inquilinus limosus, a rare organism found in patients with CF. COURSE: I. limosus treatment was deferred. Despite treatment of other pathogens, symptoms worsened. I. limosus was targeted with meropenem, amikacin, and ciprofloxacin along with clindamycin for MRSA colonization. Within weeks, symptoms had resolved with ppFEV1 improvement. DISCUSSION: This case discusses the importance of a rare organism in the CF population. Targeting I. limosus was key to recovery, revealing its potential pathogenicity.
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spelling pubmed-62193912019-07-01 Potential pathogenicity of Inquilinus limosus in a pediatric patient with cystic fibrosis Poore, T. Spencer Virella‐Lowell, Isabel Guimbellot, Jennifer S. Pediatr Pulmonol Case Report Published Online PRESENTATION: Patient is a 6‐year‐old male with CF, MRSA colonization, and pancreatic insufficiency that presented with worsening ppFEV1 and systemic symptoms despite multiple interventions. BAL grew NTM, Stenotrophomonas maltophilia, and Inquilinus limosus, a rare organism found in patients with CF. COURSE: I. limosus treatment was deferred. Despite treatment of other pathogens, symptoms worsened. I. limosus was targeted with meropenem, amikacin, and ciprofloxacin along with clindamycin for MRSA colonization. Within weeks, symptoms had resolved with ppFEV1 improvement. DISCUSSION: This case discusses the importance of a rare organism in the CF population. Targeting I. limosus was key to recovery, revealing its potential pathogenicity. John Wiley and Sons Inc. 2018-05-23 2018-07 /pmc/articles/PMC6219391/ /pubmed/29790674 http://dx.doi.org/10.1002/ppul.24043 Text en © 2018 Wiley Periodicals, Inc. This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.
spellingShingle Case Report Published Online
Poore, T. Spencer
Virella‐Lowell, Isabel
Guimbellot, Jennifer S.
Potential pathogenicity of Inquilinus limosus in a pediatric patient with cystic fibrosis
title Potential pathogenicity of Inquilinus limosus in a pediatric patient with cystic fibrosis
title_full Potential pathogenicity of Inquilinus limosus in a pediatric patient with cystic fibrosis
title_fullStr Potential pathogenicity of Inquilinus limosus in a pediatric patient with cystic fibrosis
title_full_unstemmed Potential pathogenicity of Inquilinus limosus in a pediatric patient with cystic fibrosis
title_short Potential pathogenicity of Inquilinus limosus in a pediatric patient with cystic fibrosis
title_sort potential pathogenicity of inquilinus limosus in a pediatric patient with cystic fibrosis
topic Case Report Published Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219391/
https://www.ncbi.nlm.nih.gov/pubmed/29790674
http://dx.doi.org/10.1002/ppul.24043
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