Chen Ju-Hsin, Wang Kuo-Hsien, Hu Chung-Hong, Chiu Jainn-Shiun
Department of Dermatology, Taipei Municipal Wan-Fang Hospital, Taipei Medical University, Taipei, Taiwan.
Yonsei Med J. 2008 Jun 30;49(3):509-13. doi: 10.3349/ymj.2008.49.3.509.
Angioma serpiginosum is an uncommon, acquired vascular nevoid disorder with capillary dilation and proliferation in the papillary dermis. The eruptions are asymptomatic and characterized by grouped, erythematous to violaceous, serpiginous and punctate macules. The condition usually appears in females during adolescence on unilateral lower extremities and the buttocks. We report a rare case with a late onset and atypical distribution of lesions in a 48-year-old female patient who had groups of punctate lesions on her left foot for four to five years. Histopathological examination showed hyperkeratosis and multiple dilated and proliferated capillaries in the papillary dermis. Inflammation and extravasation of red blood cells were not found. According to the clinical and pathological findings, we established a diagnosis of angioma serpiginosum. She was treated with a pulsed dye laser, and the angiomatous lesions subsequently improved.
匐行性血管瘤是一种罕见的后天性血管痣样疾病,表现为乳头真皮层的毛细血管扩张和增生。皮疹无症状,其特征为成簇的、从红斑到紫蓝色的、匐行性和点状斑疹。该病通常在青春期女性的单侧下肢和臀部出现。我们报告一例罕见病例,一名48岁女性患者发病较晚且病变分布不典型,其左脚出现成簇点状病变已有四到五年。组织病理学检查显示角化过度以及乳头真皮层有多个扩张和增生的毛细血管。未发现炎症和红细胞外渗。根据临床和病理表现,我们诊断为匐行性血管瘤。她接受了脉冲染料激光治疗,随后血管瘤性病变有所改善。