De Dipankar, Kanwar Amrinder J, Saikia Uma Nahar
Department of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
J Cutan Med Surg. 2008 Sep-Oct;12(5):249-52. doi: 10.2310/7750.2008.07035.
Darier disease is an autosomal dominant skin disorder characterized by keratotic papules, focal loss of adhesion, and abnormal keratinization. Several clinical variants of Darier disease have been described. Predominant flexural distribution of lesions in Darier disease is uncommon.
We report a sporadic case of Darier disease in which the lesions were strictly localized to the flexures. We also briefly review the differential diagnoses of such atypical localization.
A 26-year-old female presented with erythematous and hyperpigmented papular lesions localized to flexures for 4 months. The skin of the other areas, hairs, nails, and mucosa was normal. Histopathologic examination revealed suprabasal acantholysis along with dyskeratotic keratinocytes, consistent with Darier disease.
Physicians should be aware of such atypical localizations and should consider the diagnosis of flexural Darier disease along with more common clinical conditions with flexural localization, such as Hailey-Hailey disease and occasionally Grover disease.
Darier病是一种常染色体显性遗传性皮肤病,其特征为角化性丘疹、局部黏附丧失及异常角化。已描述了Darier病的几种临床变型。Darier病皮损以屈侧为主分布的情况并不常见。
我们报告1例散发性Darier病,其皮损严格局限于屈侧。我们还简要回顾了这种非典型皮损部位的鉴别诊断。
1名26岁女性,屈侧出现红斑及色素沉着性丘疹皮损4个月。身体其他部位皮肤、毛发、指甲及黏膜均正常。组织病理学检查显示基底层上棘层松解伴角化不良角质形成细胞,符合Darier病。
医生应了解这种非典型皮损部位情况,在诊断屈侧部位病变时,除了更常见的屈侧部位疾病如Hailey-Hailey病及偶尔的Grover病外,还应考虑屈侧Darier病的诊断。