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Felty’s syndrome – a rare case of febrile neutropenia

Felty’s syndrome (rheumatoid arthritis with neutropenia and splenomegaly) is a rare condition with poor long-term prognosis, mainly as a result of severe infection risk. An effective treatment strategy has not been developed so far and current treatment options are based upon case reports, small ser...

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Autores principales: Rodrigues, Luís, da Silva, Glória Nunes, de Lacerda, António Pais
Formato: Online Artículo Texto
Lenguaje:English
Publicado: UMF “Gr. T. Popa” Iasi Publishing House 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8565701/
https://www.ncbi.nlm.nih.gov/pubmed/34754908
http://dx.doi.org/10.22551/2019.23.0602.10153
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author Rodrigues, Luís
da Silva, Glória Nunes
de Lacerda, António Pais
author_facet Rodrigues, Luís
da Silva, Glória Nunes
de Lacerda, António Pais
author_sort Rodrigues, Luís
collection PubMed
description Felty’s syndrome (rheumatoid arthritis with neutropenia and splenomegaly) is a rare condition with poor long-term prognosis, mainly as a result of severe infection risk. An effective treatment strategy has not been developed so far and current treatment options are based upon case reports, small series and clinical experience since no randomized clinical trials are available. The authors describe the case of a 53-year-old female patient with a 14-year history of rheumatoid arthritis presenting with fever, neutropenia and splenomegaly. Broad-spectrum antibiotics and granulocyte colony-stimulating factor were administered with good clinical outcome and low dose methotrexate for disease control was successfully initiated after discharge. We would like to highlight the importance of being aware of this syndrome in the differential diagnosis of long term rheumatoid arthritis patients presenting with febrile neutropenia.
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spelling pubmed-85657012021-11-08 Felty’s syndrome – a rare case of febrile neutropenia Rodrigues, Luís da Silva, Glória Nunes de Lacerda, António Pais Arch Clin Cases Case Report Felty’s syndrome (rheumatoid arthritis with neutropenia and splenomegaly) is a rare condition with poor long-term prognosis, mainly as a result of severe infection risk. An effective treatment strategy has not been developed so far and current treatment options are based upon case reports, small series and clinical experience since no randomized clinical trials are available. The authors describe the case of a 53-year-old female patient with a 14-year history of rheumatoid arthritis presenting with fever, neutropenia and splenomegaly. Broad-spectrum antibiotics and granulocyte colony-stimulating factor were administered with good clinical outcome and low dose methotrexate for disease control was successfully initiated after discharge. We would like to highlight the importance of being aware of this syndrome in the differential diagnosis of long term rheumatoid arthritis patients presenting with febrile neutropenia. UMF “Gr. T. Popa” Iasi Publishing House 2021-10-27 /pmc/articles/PMC8565701/ /pubmed/34754908 http://dx.doi.org/10.22551/2019.23.0602.10153 Text en https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Rodrigues, Luís
da Silva, Glória Nunes
de Lacerda, António Pais
Felty’s syndrome – a rare case of febrile neutropenia
title Felty’s syndrome – a rare case of febrile neutropenia
title_full Felty’s syndrome – a rare case of febrile neutropenia
title_fullStr Felty’s syndrome – a rare case of febrile neutropenia
title_full_unstemmed Felty’s syndrome – a rare case of febrile neutropenia
title_short Felty’s syndrome – a rare case of febrile neutropenia
title_sort felty’s syndrome – a rare case of febrile neutropenia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8565701/
https://www.ncbi.nlm.nih.gov/pubmed/34754908
http://dx.doi.org/10.22551/2019.23.0602.10153
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