Lee Solam, Choe Sung Jay, Ahn Sung Ku
Department of Dermatology, Wonju Severance Christian Hospital, Yonsei University Wonju College of Medicine, Wonju, Korea.
Ann Dermatol. 2017 Feb;29(1):91-94. doi: 10.5021/ad.2017.29.1.91. Epub 2017 Feb 3.
Focal dermal hypoplasia, caused by mutations in , is an X-linked ectodermal dysplasia, also known as Goltz syndrome. Only seven cases of unilateral or almost unilateral focal dermal hypoplasia have been reported in the English literature and there have been no previously reported cases in the Republic of Korea. A 19-year-old female presented with scalp defects, skin lesions on the right leg and the right trunk, and syndactyly of the right fourth and fifth toes. Cutaneous examination revealed multiple atrophic plaques and a brown and yellow mass with fat herniation and telangiectasia that was mostly located on the lower right leg. She had syndactyly on the right foot and the scalp lesion appeared to be an atrophic, membranous, fibrotic alopecic scar. A biopsy of the calf revealed upper dermal extension of fat cells, dermal atrophy, and loss of dermal collagen. A diagnosis of almost unilateral focal dermal hypoplasia was made on the basis of physical and histologic findings. Henceforth, the patient was referred to a plastic surgeon and an orthopedics department to repair her syndactyly.
由 基因突变引起的局灶性真皮发育不全是一种 X 连锁外胚层发育不良,也称为戈尔茨综合征。英文文献中仅报道了 7 例单侧或几乎单侧局灶性真皮发育不全病例,韩国此前尚无相关病例报道。一名 19 岁女性患者出现头皮缺损、右腿和右躯干皮肤病变以及右足第四和第五趾并指畸形。皮肤检查发现多个萎缩性斑块以及一个伴有脂肪疝出和毛细血管扩张的棕黄色肿块,主要位于右小腿下部。她右足存在并指畸形,头皮病变似乎是一个萎缩性、膜状、纤维化的脱发瘢痕。小腿活检显示脂肪细胞向真皮上层延伸、真皮萎缩以及真皮胶原蛋白缺失。根据体格检查和组织学检查结果诊断为几乎单侧局灶性真皮发育不全。此后,该患者被转诊至整形外科医生和骨科,以修复其并指畸形。