Hemophagocytic lymphohistiocytosis accompanying Still's disease: A case report

Hemophagocytic lymphohistiocytosis (HLH) is a rare hematologic disease that occurs due to immune system dysfunction. Clinical manifestations of this disease are fever, increased ferritin level, cytopenia, and hemophagocytosis in the biopsy report of the bone marrow. We report a 36‐year‐old woman ref...

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Autores principales: Ahmadzadeh, Arman, Babadi, Neda, Farsad, Faraneh, Babadi, Saba, Assar, Shirin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565094/
https://www.ncbi.nlm.nih.gov/pubmed/37830072
http://dx.doi.org/10.1002/ccr3.7955
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author Ahmadzadeh, Arman
Babadi, Neda
Farsad, Faraneh
Babadi, Saba
Assar, Shirin
author_facet Ahmadzadeh, Arman
Babadi, Neda
Farsad, Faraneh
Babadi, Saba
Assar, Shirin
author_sort Ahmadzadeh, Arman
collection PubMed
description Hemophagocytic lymphohistiocytosis (HLH) is a rare hematologic disease that occurs due to immune system dysfunction. Clinical manifestations of this disease are fever, increased ferritin level, cytopenia, and hemophagocytosis in the biopsy report of the bone marrow. We report a 36‐year‐old woman referred to our hospital with persistent fever, arthralgia in interphalangeal joints, and cutaneous rash on the trunk, was subsequently diagnosed as an adult‐onset Still's disease (AOSD), and after bone marrow aspiration, HLH was diagnosed with her.
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spelling pubmed-105650942023-10-12 Hemophagocytic lymphohistiocytosis accompanying Still's disease: A case report Ahmadzadeh, Arman Babadi, Neda Farsad, Faraneh Babadi, Saba Assar, Shirin Clin Case Rep Case Report Hemophagocytic lymphohistiocytosis (HLH) is a rare hematologic disease that occurs due to immune system dysfunction. Clinical manifestations of this disease are fever, increased ferritin level, cytopenia, and hemophagocytosis in the biopsy report of the bone marrow. We report a 36‐year‐old woman referred to our hospital with persistent fever, arthralgia in interphalangeal joints, and cutaneous rash on the trunk, was subsequently diagnosed as an adult‐onset Still's disease (AOSD), and after bone marrow aspiration, HLH was diagnosed with her. John Wiley and Sons Inc. 2023-10-10 /pmc/articles/PMC10565094/ /pubmed/37830072 http://dx.doi.org/10.1002/ccr3.7955 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ahmadzadeh, Arman
Babadi, Neda
Farsad, Faraneh
Babadi, Saba
Assar, Shirin
Hemophagocytic lymphohistiocytosis accompanying Still's disease: A case report
title Hemophagocytic lymphohistiocytosis accompanying Still's disease: A case report
title_full Hemophagocytic lymphohistiocytosis accompanying Still's disease: A case report
title_fullStr Hemophagocytic lymphohistiocytosis accompanying Still's disease: A case report
title_full_unstemmed Hemophagocytic lymphohistiocytosis accompanying Still's disease: A case report
title_short Hemophagocytic lymphohistiocytosis accompanying Still's disease: A case report
title_sort hemophagocytic lymphohistiocytosis accompanying still's disease: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565094/
https://www.ncbi.nlm.nih.gov/pubmed/37830072
http://dx.doi.org/10.1002/ccr3.7955
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