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- Title
adult case of suspected A20 haploinsufficiency mimicking polyarteritis nodosa.
- Authors
Niwano, Tomoko; Hosoya, Tadashi; Kadowaki, Saori; Toyofuku, Etsushi; Naruto, Takuya; Shimizu, Masaki; Ohnishi, Hidenori; Koike, Ryuji; Morio, Tomohiro; Imai, Kohsuke; Yoshida, Masayuki; Yasuda, Shinsuke
- Abstract
The article presents a case report of a young Japanese female with suspected A20 haploinsufficiency (HA20) who was diagnosed after a recurrent myocardial infarction. The patient had multiple occlusions and aneurysms in her abdominal arteries resembling polyarteritis nodosa. It is difficult to make an exact diagnosis in atypical autoinflammatory disorder until a typical event or complication occurs as HA20 can mimic various autoimmune diseases.
- Subjects
MYOCARDIAL infarction complications; CELL metabolism; PHYSICAL diagnosis; GENETIC mutation; PREDNISOLONE; SEQUENCE analysis; MYOCARDIAL infarction; IMMUNOBLOTTING; POLYARTERITIS nodosa; TUMOR necrosis factors; DRUG therapy; ROUTINE diagnostic tests; ADALIMUMAB; AUTOINFLAMMATORY diseases; GOLIMUMAB
- Publication
Rheumatology, 2022, Vol 61, Issue 11, pe337
- ISSN
1462-0324
- Publication type
Case Study
- DOI
10.1093/rheumatology/keac308