Hirota T, Hirota Y, Asagami C, Muto M
Department of Dermatology, Yamaguchi University School of Medicine, Ube, Japan.
J Dermatol. 1998 Mar;25(3):163-6. doi: 10.1111/j.1346-8138.1998.tb02373.x.
A 5-day-old Japanese female with Neu-Laxova syndrome was presented. The patient had severe edema throughout the body, desquamation, and erosion of the skin. She also exhibited microcephaly, exophthalmos, and rocker-bottom feet. Histologic examinations of a cutaneous specimen showed atrophy of the dermis and absence of the sebaceous glands. These represent embryonic abnormalities. Even though there was no hypoplasia of the cerebellum and lungs or hydramnios, we evaluated this patient as the first Japanese case of this sporadic disease. With intensive care, including dermatological treatment, the patient survived for 134 days.
本文报告了一名患有Neu-Laxova综合征的5日龄日本女性婴儿。该患者全身出现严重水肿、皮肤脱屑和糜烂。她还表现出小头畸形、眼球突出和摇椅底足。皮肤标本的组织学检查显示真皮萎缩和皮脂腺缺失。这些均代表胚胎发育异常。尽管该患者没有小脑和肺部发育不全或羊水过多的情况,但我们仍将其评估为日本首例该散发性疾病患者。经过包括皮肤科治疗在内的重症监护,该患者存活了134天。