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棘层松解性皮肤病的鉴别组织病理学特征及棘层松解性颗粒层增生模式。

Distinguishing histopathologic features of acantholytic dermatoses and the pattern of acantholytic hypergranulosis.

作者信息

See Sharlene Helene C, Peternel Sandra, Adams Derrick, North Jeffrey P

机构信息

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

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

出版信息

J Cutan Pathol. 2019 Jan;46(1):6-15. doi: 10.1111/cup.13356. Epub 2018 Nov 5.

Abstract

BACKGROUND

Acantholysis can be seen in multiple skin diseases. Adnexal acantholysis has been regarded as a feature distinguishing pemphigus vulgaris (PV) from acantholytic conditions.

METHODS

A retrospective review of the histopathologic features of diseases with acantholysis including PV, pemphigus foliaceus (PF), Hailey-Hailey disease (HHD), Darier disease (DD), Grover disease, and pityriasis rubra pilaris (PRP) was performed.

RESULTS

Biopsies of PV (n = 49), HHD (n = 27), DD (n = 25), Grover disease (n = 65), and PRP (n = 33) showed suprabasilar acantholysis. Acantholysis was limited to the lower epidermis in PV and PRP, and involved all epidermal layers in HHD, DD, and Grover disease. Acantholysis in PF (n = 38) mainly involved the upper epidermis. Follicular acantholysis occurred more frequently in PV and PF (P < 0.0001). Eccrine acantholysis was found in PV (42%), HHD (18%), PF (13%), and DD (4%). Grover disease, DD, and HHD had greater dyskeratosis (P < 0.0001). Neutrophils were more common in PV, PF, and HHD, while eosinophils were more common in Grover disease and DD. A pattern termed acantholytic hypergranulosis occurred predominantly in PF.

CONCLUSION

Adnexal acantholysis does not reliably distinguish PV from PF. The level of acantholysis, degree of dyskeratosis, and acantholytic hypergranulosis are distinguishing features between the two types of pemphigus and other acantholytic disorders.

摘要

背景

棘层松解可见于多种皮肤疾病。附属器棘层松解被视为寻常型天疱疮(PV)与棘层松解性疾病相鉴别的一项特征。

方法

对包括PV、落叶型天疱疮(PF)、黑棘皮病(HHD)、毛囊角化病(DD)、Grover病和毛发红糠疹(PRP)在内的伴有棘层松解的疾病的组织病理学特征进行回顾性分析。

结果

PV(n = 49)、HHD(n = 27)、DD(n = 25)、Grover病(n = 65)和PRP(n = 33)的活检显示基底上棘层松解。PV和PRP的棘层松解局限于表皮下部,而HHD、DD和Grover病的棘层松解累及所有表皮层。PF(n = 38)的棘层松解主要累及表皮上部。毛囊棘层松解在PV和PF中更常见(P < 0.0001)。在PV(42%)、HHD(18%)、PF(13%)和DD(4%)中发现了小汗腺棘层松解。Grover病、DD和HHD有更严重的角化不良(P < 0.0001)。中性粒细胞在PV、PF和HHD中更常见,而嗜酸性粒细胞在Grover病和DD中更常见。一种称为棘层松解性角化过度的模式主要出现在PF中。

结论

附属器棘层松解不能可靠地将PV与PF区分开来。棘层松解的程度、角化不良的程度和棘层松解性角化过度是两种天疱疮类型与其他棘层松解性疾病之间的鉴别特征。

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