毛囊性银屑病的系统评价:一种独特但未被充分认识的实体

Q3 Medicine Journal of Psoriasis and Psoriatic Arthritis Pub Date : 2023-10-01 Epub Date: 2023-08-24 DOI:10.1177/24755303231196567
Kelli Jablon, Jonathan D Ho, Hye Jin Chung
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引用次数: 0

摘要

毛囊性牛皮癣(FP)是一种罕见且未被充分认识的牛皮癣亚型,它影响毛囊,由于其独特的表现,经常被误诊。我们的目的是分析经常报道的FP的临床、组织学和皮肤镜特征,以及他们的治疗方案。我们对PubMed/MEDLINE数据库进行了系统的检索,检索词为“滤泡性”和“牛皮癣”。14项研究纳入了44例患者(27例成人[61.4%]和17例儿童[38.6%])的信息。成年FP以女性为主(M:F = 1:7 .7),经常累及下肢(81.5%),与代谢综合征(包括糖尿病)相关(22.2%),偏爱有色皮肤(SOC:白色= 8:1)。相反,幼年型FP表现为雄性优势(M:F = 1:6 .6),常累及躯干(41.2%),只累及有色皮肤(SOC:White = 11:0)。除了其独特的表现外,由于其伴发牛皮癣的发生率低(31.8%),以及罕见的个人(18.2%)或家族史(6.8%),FP容易被误诊。报告的组织病理学特征包括角化性堵塞,滤泡角化不全伴或不伴中性粒细胞,牛皮癣状棘层病,低颗粒病和滤泡上皮中性粒细胞浸润。皮镜检查结果包括毛囊中心病变,终末毛外观正常,毛囊周围白色鳞片和各种血管结构。一旦正确诊断,FP患者通过局部和全身治疗的各种组合表现出症状的改善或缓解。了解FP的人口学特征和临床表现可以帮助解决对这种牛皮癣临床变体的认识不足。
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A Systematic Review of Follicular Psoriasis: A Unique but Under-Recognized Entity.

Background: Follicular psoriasis (FP) is a rare and under-recognized subtype of psoriasis that affects hair follicles and can be frequently misdiagnosed due to its unique presentation.

Objective: We aimed to analyze the frequently reported clinical, histological, and dermatoscopic features of FP, as well as their treatment options.

Methods: We conducted a systematic review of the PubMed/MEDLINE database using the search terms "follicular" and "psoriasis." Fourteen studies were included yielding information on 44 patients (27 adults [61.4%] and 17 children [38.6%]).

Results: Adult FP showed a female predominance (M:F = 1:2.7), frequent involvement of lower extremities (81.5%), association with metabolic syndrome including diabetes mellitus (22.2%), and a predilection for skin of color (SOC:White = 8:1). On the contrary, juvenile FP revealed male predominance (M:F = 1:0.6), frequent involvement of the trunk (41.2%), and exclusive involvement in skin of color (SOC:White = 11:0). In addition to its unique presentation, FP tends to be misdiagnosed due to its low incidence of concomitant psoriasis (31.8%), and rare personal (18.2%) or family history (6.8%) of psoriasis. Reported histopathological features include keratotic plugging, follicular parakeratosis with or without neutrophils, psoriasiform acanthosis, hypogranulosis, and neutrophilic infiltration of follicular epithelium. Dermatoscopic findings include folliculocentric lesions with normal appearing terminal hairs, perifollicular white scale, and various vascular structures.

Conclusion: Once correctly diagnosed, patients with FP showed improvement or resolution of symptoms with various combinations of topical and systemic therapies. Understanding the demographic features and clinical presentations of FP can help address under-recognition of this clinical variant of psoriasis.

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CiteScore
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19
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