Research Unit Dermatopathology, Department of Dermatology, Medical University of Graz, Graz, Austria; and.
Department of Dermatology, Scientific Institute for Research, Hospitalization and Healthcare (IRCCS) - INRCA, Ancona, Italy.
Am J Dermatopathol. 2020 May;42(5):e61-e64. doi: 10.1097/DAD.0000000000001534.
Identification of subtle disease-specific histologic changes may be of significant help in early diagnosis of acantholytic skin diseases. Hailey-Hailey disease (HHD) is an autosomal dominant genodermatosis characterized by vesiculoerosive lesions favoring the intertriginous areas. Histologically, HHD is characterized by full-thickness acantholysis of the spinous layer in association with dyskeratosis of individual keratinocytes; a pemphigus vulgaris-like suprabasal pattern of acantholysis may be observed in the earliest stages of disease. HHD is characterized by highly variable expressivity regarding the age at onset and severity of the disease. Patients may present with late-onset and/or only mild disease. We report the recurrent presence of incidental foci of variably extensive, subclinical acantholysis in multiple bioptic specimens taken from a patient with known HHD for dermatologic conditions other than HHD. Such histologic finding has gone underappreciated in the literature, despite being a likely frequent occurrence in skin biopsies from HHD patients; recognition of this finding might represent a valuable diagnostic clue in selected cases of HHD.
识别细微的疾病特异性组织学变化可能对汗孔角化病的早期诊断有重要帮助。Hailey-Hailey 病(HHD)是一种常染色体显性遗传皮肤病,其特征为水疱糜烂性病变,好发于皱褶部位。组织学上,HHD 的特征是棘层全层松解,伴有个别角质形成细胞的角化不良;在疾病的早期阶段,可能观察到寻常型天疱疮样棘层松解的超基底层模式。HHD 发病年龄和疾病严重程度的表现具有高度可变性。患者可能表现为发病晚和/或仅有轻度疾病。我们报告了一例已知患有 HHD 的患者,在接受皮肤科疾病的多次活检中,反复出现偶然的、不同程度的亚临床棘层松解灶。尽管这种组织学发现可能是 HHD 患者皮肤活检中的常见现象,但在文献中并未得到充分重视;在某些特定的 HHD 病例中,认识到这一发现可能是一个有价值的诊断线索。