Hemophagocytic lymphohistiocytosis accompanying Still's disease: A case report.
adult‐onset Still's disease
hemophagocytic lymphohistiocytosis
Journal
Clinical case reports
ISSN: 2050-0904
Titre abrégé: Clin Case Rep
Pays: England
ID NLM: 101620385
Informations de publication
Date de publication:
Oct 2023
Oct 2023
Historique:
received:
29
05
2023
revised:
07
07
2023
accepted:
12
09
2023
medline:
13
10
2023
pubmed:
13
10
2023
entrez:
13
10
2023
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 37830072
doi: 10.1002/ccr3.7955
pii: CCR37955
pmc: PMC10565094
doi:
Types de publication
Case Reports
Langues
eng
Pagination
e7955Informations de copyright
© 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.
Déclaration de conflit d'intérêts
The authors declare that they have no competing interests.
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