Department of Oncology and Metabolism, The University of Sheffield, Sheffield, UK
Department of Ophthalmology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
BMJ Case Rep. 2020 Oct 22;13(10):e236741. doi: 10.1136/bcr-2020-236741.
An elderly white man with a history of left oculodermal melanocytosis presented with new onset brown pigmentation of the left bulbar and inferior tarsal conjunctiva. The bulbar conjunctival pigmentation was at the level of the conjunctival epithelium and was overlying areas of typical slate-grey scleral pigmentation characteristic of oculodermal melanocytosis. Both areas of new pigmentation were biopsied. The bulbar conjunctiva revealed primary acquired melanosis (PAM) without atypia with increased melanin production and the tarsal conjunctival biopsy showed PAM without atypia sine pigmentio overlying areas of substantia propria spindle-shaped heavily pigmented melanocytes of oculodermal melanocytosis. The case report examines the relationship between the epithelial and substantia propria melanocytes and correlates the findings with what is known about this association from the dermatopathology literature.
一位老年白人男性,有左眼皮肤黑素细胞增多症病史,现出现左眼球结膜和下睑结膜新出现褐色色素沉着。球结膜色素沉着位于结膜上皮层,覆盖典型石板灰色巩膜色素沉着区域,这是眼皮肤黑素细胞增多症的特征。两个新出现的色素沉着区域均进行了活检。球结膜显示原发性获得性黑色素增多症(PAM),无非典型性,黑色素生成增加,而睑结膜活检显示 PAM 无非典型性色素缺失,覆盖眼皮肤黑素细胞增多症固有层梭形重度色素沉着的黑色素细胞。该病例报告检查了上皮细胞和固有层黑色素细胞之间的关系,并将这些发现与从皮肤病理学文献中了解到的关于这种关联的信息进行了比较。