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额部纤维性脱发。

Frontal fibrosing alopecia.

机构信息

Sinclair Dermatology, East Melbourne, Victoria, Australia.

Sinclair Dermatology, East Melbourne, Victoria, Australia.

出版信息

Clin Dermatol. 2021 Mar-Apr;39(2):183-193. doi: 10.1016/j.clindermatol.2020.10.007. Epub 2020 Oct 17.

Abstract

Frontal fibrosing alopecia (FFA) is a patterned primary cicatricial alopecia that was first described in 1994. Once rare, the incidence of FFA has increased dramatically, representing the current most common cause of cicatricial alopecia worldwide. FFA typically begins in postmenopausal women with symmetrical, progressive recession of the frontotemporal hairline together with bilateral loss of the eyebrows. FFA has a distinctive clinical phenotype, which remains a challenge. The histology is identical to lichen planopilaris (LPP), but only a small number of patients have coincidental LPP, usually of the scalp. The vast majority of patients have no evidence of lichen planus elsewhere, and the symmetry and patterned nature of the hair loss are unusual for LPP. Familial cases of FFA are reported, and gene associations have been identified in population studies; however, the pathophysiology remains controversial. Without treatment, FFA is slowly progressive, and although many treatments have been prescribed, the response is often disappointing. We review the pathogenesis, epidemiology, clinical features, histology, and treatment of FFA.

摘要

额部纤维性脱发(FFA)是一种定型性原发性瘢痕性脱发,于 1994 年首次描述。FFA 曾经罕见,但发病率已显著增加,是目前全球最常见的瘢痕性脱发原因。FFA 通常发生于绝经后女性,表现为额颞部发际线进行性对称退缩,同时双侧眉毛脱落。FFA 具有独特的临床表型,这仍然是一个挑战。其组织学与扁平苔藓样瘢痕性脱发(LPP)相同,但只有少数患者同时存在 LPP,通常为头皮受累。绝大多数患者其他部位无扁平苔藓证据,脱发的对称性和定型性对 LPP 来说不常见。已有家族性 FFA 病例报道,并在人群研究中发现了基因相关性;然而,其发病机制仍存在争议。未经治疗时,FFA 进展缓慢,尽管已开出许多治疗方案,但反应通常令人失望。我们对 FFA 的发病机制、流行病学、临床特征、组织学和治疗进行了综述。

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