An adult case of atypical familial Mediterranean fever (pyrin‐associated autoinflammatory disease) similar to adult‐onset Still’s disease

Tytuł:: An adult case of atypical familial Mediterranean fever (pyrin‐associated autoinflammatory disease) similar to adult‐onset Still’s disease
Autorzy:: Hayato Tsuruma
Hiroe Sato
Eriko Hasegawa
Yukiko Nozawa
Takeshi Nakatsue
Yoko Wada
Takeshi Kuroda
Yoshiki Suzuki
Masaaki Nakano
Ichiei Narita
Temat:: adult‐onset Still’s disease
elevated liver enzymes
Familial Mediterranean fever
pyrin‐associated autoinflammatory diseases
skin rash
Medicine
Medicine (General)
R5-920
Źródło:: Clinical Case Reports, Vol 7, Iss 4, Pp 801-805 (2019)
Wydawca:: Wiley, 2019.
Rok publikacji:: 2019
Kolekcja:: LCC:Medicine
LCC:Medicine (General)
Typ dokumentu:: article
Opis pliku:: electronic resource
Język:: English
ISSN:: 2050-0904
Relacje:: https://doaj.org/toc/2050-0904
DOI:: 10.1002/ccr3.2102
Dostęp URL:: https://doaj.org/article/5720f840bd6d4ac99d143adc84ba4035 Link otwiera się w nowym oknie
Numer akcesji:: edsdoj.5720f840bd6d4ac99d143adc84ba4035
: Czasopismo naukowe

Pełny tekst

Key Clinical Message We present a 55‐year‐old woman with periodic fever and symptoms similar to adult‐onset Still's disease (AOSD). She had a heterogeneous mutation of the MEFV gene and colchicine was effective. Atypical familial Mediterranean fever (pyrin‐associated autoinflammatory disease) should be considered in patients with periodic fever accompanied by symptoms similar to AOSD.

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