Fukai K, Hamada T, Ishii M, Kitajima J, Terao Y
Department of Dermatology, Osaka City University Medical School, Japan.
Acta Derm Venereol. 1989;69(6):524-7.
Two cases of piebaldism are reported. The first patient was a 9-month-old girl with inborn hypopigmented areas on the frontal region of the scalp and both knees. There were no melanocytes in the lesions. In the second case, we observed the patient from 2 months of age for a period of 9 years. Many hyperpigmented spots appeared on the hypomelanotic areas on the frontal region of the scalp, abdomen and both knees. Electron-microscopic examinations of the hypomelanotic skin disclosed an area with regularly distributed melanocytes as well as an area with no melanocytes. Most of the melanosomes were ellipsoidal and lamellar. They were in stage II to III, which signified delayed pigmentation. Hyperpigmented spots were slightly enlarged following PUVA treatment.
报告了两例斑驳病病例。首例患者为一名9个月大的女孩,头皮额部和双膝关节先天性色素减退。病变部位无黑素细胞。第二例患者,我们从2个月大开始观察,观察期为9年。头皮额部、腹部和双膝关节的色素减退区域出现了许多色素沉着斑。对色素减退皮肤进行电子显微镜检查发现,存在黑素细胞分布规则的区域以及无黑素细胞的区域。大多数黑素小体呈椭圆形且有板层结构。它们处于II至III期,这表明色素沉着延迟。经补骨脂素加长波紫外线(PUVA)治疗后,色素沉着斑略有增大。