由DOCK8免疫缺陷综合征驱动的亲毛囊蕈样肉芽肿

Folliculotropic mycosis fungoides driven by DOCK8 immunodeficiency syndrome.

作者信息

Rubio-Gonzalez Belen, Frieden Ilona J, McCalmont Timothy H, Dorsey Morna, Funk Tracy, Pincus Laura B

机构信息

Department of Pathology, University of California San Francisco, San Francisco, CA, USA.

Department of Dermatology, University of California San Francisco, San Francisco, CA, USA.

出版信息

Pediatr Dermatol. 2021 Jan;38(1):229-232. doi: 10.1111/pde.14424. Epub 2020 Oct 25.

DOI:10.1111/pde.14424

PMID:33099799

Abstract

DOCK8 immunodeficiency syndrome (DIDS) represents a rare primary immunodeficiency associated with cutaneous viral infections, allergy, and increased risk of malignancy. We report a case of folliculotropic mycosis fungoides with spontaneous resolution occurring in a patient with DIDS.

摘要

DOCK8免疫缺陷综合征（DIDS）是一种罕见的原发性免疫缺陷病，与皮肤病毒感染、过敏及恶性肿瘤风险增加相关。我们报告了1例发生于DIDS患者的亲毛囊性蕈样肉芽肿自发缓解病例。