| Literature DB >> 31030362 |
Ertao Jia1,2, Jiaxin Wei3, Hongling Geng4, Xia Qiu5,3, Jingjing Xie5,3, Yuya Xiao5,3, Li Zhong5,3, Min Xiao5,3, Yanying Zhang5,3, Yubao Jiang5,3, Jianyong Zhang6,7.
Abstract
Anti-small ubiquitin-like modifier-1 activating enzyme (anti-SAE) antibodies have been recently discovered especially for myosin and identified as dermatomyositis (DM) marker. The frequency of anti-SAE antibodies in DM patients is extremely low. Diffuse pruritic erythema may be one kind of clinical manifestations of DM with anti-SAE antibodies. In this report, a 48-year-old female patient with amyopathic dermatomyositis (ADM) carrying anti-SAE antibodies presented diffuse pruritic erythema for 5 months. Diffuse pruritic erythema improved after treatment with prednisolone, cyclosporine, and thalidomide. The clinical characteristics of 75 previously reported cases with anti-SAE antibody-positive DM were reviewed, and the manifestations of the Asian and Western cohorts were compared. It was revealed that the Asian patients were more susceptible to diffuse erythema (17/34 vs. 3/41, P = 0.000), dysphagia (16/34 vs. 10/41, P = 0.040), and interstitial lung disease (ILD) (21/34 vs. 5/41, P = 0.000) compared with the Western patients. The frequency of malignancy in the Asian cohort was significantly higher than that in the Western cohort (10/34 vs. 4/41, P = 0.030).Entities:
Keywords: Anti-SAE antibody; Anti-small ubiquitin-like modifier-1 activating enzyme antibody; Dermatomyositis; Diffuse erythema; Literature review; Malignancy
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Year: 2019 PMID: 31030362 DOI: 10.1007/s10067-019-04562-w
Source DB: PubMed Journal: Clin Rheumatol ISSN: 0770-3198 Impact factor: 2.980