Acantholytic Dyskeratoses of the Vulva: Clinicopathologic Characterization of 16 Cases and Review of the Literature.

IF 1.6 4区 医学 Q3 OBSTETRICS & GYNECOLOGY
Maxwell D Wang, Scott C Bresler, May P Chan, Rajiv M Patel, David B Chapel
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引用次数: 0

Abstract

The vulva and perineum are rarely involved by acantholytic dyskeratoses, including Hailey-Hailey disease, Darier disease, papular acantholytic dyskeratosis of the genitocrural area, acantholytic dyskeratotic acanthoma, and warty dyskeratoma. These entities show broad histomorphologic overlap, generally requiring clinical correlation for definitive classification. This institutional series aims to better characterize vulvar acantholytic dyskeratoses and provide a practical literature review and diagnostic aid for gynecologic pathologists. Our institutional archives contained 16 vulvar acantholytic dyskeratoses diagnosed between 1990 and 2023. Affected patients were 36 to 79 (mean, 58) years old and presented with one or more asymptomatic (n = 9) or pruritic (n = 6) lesions involving the vulva (predominantly the labia majora), with additional perineal involvement in 2. Four patients have known Hailey-Hailey disease. Eleven cases comprised singular, raised, erythematous, or skin-colored papules, measuring 0.2 to 0.6 (mean, 0.3) cm. Two patients had oligofocal (both with known Hailey-Hailey disease) vulvar lesions, and 2 had multifocal vulvar lesions (one with known Hailey-Hailey disease). Histologically, all showed acantholysis and dyskeratoses (abundant in 8, focal in 8, with corps ronds generally more conspicuous than corps grains). Additional features included suprabasal clefting (n = 14), dermal papillomatosis (n = 12), and acanthosis (n = 8). Adnexal involvement was rare (n = 1). No histologic features reliably distinguished sporadic versus syndromic acantholytic dyskeratoses. Sporadic lesions were cured by local excision. Patients with Hailey-Hailey disease were variably responsive to corticosteroids. Neither our series nor the literature indicate a significant correlation between sporadic or syndromic acantholytic dyskeratosis and squamous cell carcinoma. Important differential diagnoses include pemphigus vulgaris and pemphigus vegetans, for which direct immunofluorescence may be performed, when indicated.

外阴黄褐斑病变:16 例临床病理特征和文献综述。
外阴和会阴很少会被棘层溶解性角化不良所累及,包括海利-海利病、达里尔病、生殖器部位丘疹性棘层溶解性角化不良、棘层溶解性角化不良棘皮瘤和疣状角化不良瘤。这些实体在组织形态学上有广泛的重叠,通常需要临床相关性才能明确分类。本研究旨在更好地描述外阴棘层溶解性角化不良的特征,并为妇科病理学家提供实用的文献综述和诊断帮助。我们的机构档案中包含了 1990 年至 2023 年间诊断出的 16 例外阴棘层溶解性角化不良。患者年龄在 36 岁至 79 岁(平均 58 岁)之间,有一个或多个无症状(9 例)或瘙痒性(6 例)病变,累及外阴(主要是大阴唇),其中 2 例还累及会阴部。11 例病例为单发、隆起、红斑或皮肤色丘疹,大小为 0.2 至 0.6 厘米(平均 0.3 厘米)。两名患者有少灶性外阴病变(两人均患有已知的海利-海利病),两名患者有多灶性外阴病变(其中一人患有已知的海利-海利病)。从组织学角度看,所有病例都出现了棘层溶解和角化不良(8 例为大量角化不良,8 例为局灶性角化不良,角化嵴通常比角化颗粒更明显)。其他特征包括基底膜上裂(14 例)、真皮乳头状瘤病(12 例)和棘皮症(8 例)。附件受累罕见(1 例)。没有组织学特征能可靠地区分散发性和综合征性棘皮症。散发性病变可通过局部切除治愈。海利-海利病患者对皮质类固醇激素的反应不一。我们的系列研究和文献均未显示散发性或综合征性角化棘皮症与鳞状细胞癌之间存在明显的相关性。重要的鉴别诊断包括寻常天疱疮和植物性天疱疮,有必要时可进行直接免疫荧光检查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.90
自引率
12.50%
发文量
154
审稿时长
6-12 weeks
期刊介绍: International Journal of Gynecological Pathology is the official journal of the International Society of Gynecological Pathologists (ISGyP), and provides complete and timely coverage of advances in the understanding and management of gynecological disease. Emphasis is placed on investigations in the field of anatomic pathology. Articles devoted to experimental or animal pathology clearly relevant to an understanding of human disease are published, as are pathological and clinicopathological studies and individual case reports that offer new insights.
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