Frontal fibrosing alopecia: A review of 60 cases

被引:137
作者
MacDonald, Alison [1 ]
Clark, Colin [1 ]
Holmes, Susan [1 ]
机构
[1] So Gen Hosp, Alan Lyell Ctr Dermatol, Glasgow G51 4TF, Lanark, Scotland
关键词
affluence; alopecia; autoimmunity; frontal fibrosing alopecia; lichen planopilaris; origin; prognosis; treatment; LICHEN-PLANOPILARIS; THYROID-DISEASE; PREVALENCE; EFFICACY;
D O I
10.1016/j.jaad.2011.12.038
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Frontal fibrosing alopecia (FFA) is a variant of lichen planopilaris primarily affecting postmenopausal women, with a predilection for the frontotemporal hairline. Objectives: We sought to examine possible causal associations and review the clinical features, natural history, and response to treatment of patients with FFA attending a specialist hair clinic. Methods: This was a case note review of 60 patients with FFA. Results: The number of patients with FFA seen has increased over the last decade. All were Caucasian women, with significantly above-average affluence scores and were less likely to be smokers. The mean age at presentation was 64 years and average disease duration was 3.4 years (range: 6 months-30 years). Three patients were premenopausal. All patients had frontotemporal involvement, with follicular hyperkeratosis, scarring, and variable perifollicular erythema. Several patients had more unusual patterns: 8 had extensive parietal involvement, 4 had occipital involvement, 1 had asymmetric frontal involvement, and 5 had typical FFA associated with diffuse scalp lichen planopilaris. Eyebrow loss was documented in 73%, eyelash loss in 3%, and body hair loss in 25%. Almost all patients had been treated with superpotent topical steroids. Other treatments included topical calcineurin inhibitors; intralesional triamcinolone acetate; phototherapy; hydroxychloroquine; lymecycline; and prednisolone. Although some treatments may reduce inflammation, their efficacy in controlling the progress of the alopecia was uncertain. Limitations: This is a retrospective review. Conclusions: FFA is a clinically distinctive condition, the prevalence of which appears to be increasing. It has a generally poor response to treatment. The origin remains uncertain. (J Am Acad Dermatol 2012;67:955-61.)
引用
收藏
页码:955 / 961
页数:7
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