医学
免疫缺陷
自身抗体
回顾性队列研究
相伴的
免疫病理学
皮肤病科
病历
干扰素γ
免疫学
内科学
抗体
细胞因子
免疫系统
作者
Penvadee Pattanaprichakul,Charussri Leeyaphan,Nasikarn Angkasekwinai,Sumanas Bunyaratavej,Sansnee Senawong,Chutima Seree-aphinan,Kanyalak Munprom
摘要
Cutaneous findings in adult-onset immunodeficiency due to anti-interferon gamma autoantibodies (anti-IFN-γ autoAbs) are common. Currently, data on this topic are scarce.We retrospectively reviewed medical records of 202 skin episodes from 77 patients diagnosed with adult-onset immunodeficiency due to anti-IFN-γ autoAbs. The exclusion of drug eruptions left 180 episodes from 74 patients for further analysis.Reactive dermatosis was diagnosed in 66.1%, followed by disseminated skin infection (18.3%) and local skin infection (15.6%). Neutrophilic dermatosis (ND) tended to appear on the upper part of bodies, while leg lesions were common in the non-ND. Disseminated infection occurred more frequently with ND. Mycobacterium abscessus was the most common pathogen of concomitant infection. Remission was achieved in 21.6% and was significantly associated with females.Reactive dermatosis was the most common skin manifestation. ND was found in the upper part of bodies and associated with disseminated infection. Drug-free remission was scarcely achieved.
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