Department of Dermatology, Xijing Hospital, Fourth Military Medical University, Xian, China.
J Dermatol. 2013 Aug;40(8):653-6. doi: 10.1111/1346-8138.12192. Epub 2013 Jun 5.
Angiokeratoma includes a group of unrelated diseases characterized by hyperkeratosis and dilation of vessels in the superficial dermis. In this study, 21 cases of solitary lesions located on palms and soles and histopathologically diagnosed as angiokeratoma were analyzed retrospectively. All lesions presented as red to violet macules or plaques. Histopathologically, all of them showed hyperkeratosis and vascular dilation in the papillary to deep dermis. The elongated vessels were of different sizes and shape, lined by a single layer of endothelial cells. In 13 lesions, the endothelial cells protruded into the lumen, forming a hobnail appearance. Immunohistochemical study showed the endothelial cells were positive for CD31 and CD34, negative for D2-40, and focally positive for Wilms tumor 1 (WT-1) in most cases. Our cases represented a rare type of angiokeratoma located on the palms and soles, in which the focal positivity of WT-1 was different from previously reported vascular proliferations.
血管角化瘤包括一组无关联的疾病,其特征为真皮浅层的角化过度和血管扩张。本研究回顾性分析了 21 例位于手掌和足底、组织病理学诊断为血管角化瘤的孤立性病变。所有病变均表现为红色至紫色斑疹或斑块。组织病理学上,所有病变均显示角化过度和真皮浅层至深层的血管扩张。延长的血管大小和形状不一,由单层内皮细胞排列。在 13 个病变中,内皮细胞向管腔突出,呈钉突状外观。免疫组化研究显示,大多数病例的内皮细胞 CD31 和 CD34 阳性,D2-40 阴性,Wilms 瘤 1(WT-1)局灶性阳性。本病例代表一种罕见类型的位于手掌和足底的血管角化瘤,其中 WT-1 的局灶性阳性与之前报道的血管增生不同。