Tanaka H, Yasui N, Kuriskaki E, Shimomura Y
Department of Orthopaedic Surgery, National Defense Medical College, Tokorozawa Saitama, Japan.
Int Orthop. 1990;14(2):179-81. doi: 10.1007/BF00180125.
The Goltz syndrome is a rare condition in which there are congenital anomalies in skin, teeth, eyes and bone. We report an unusual case of a 17 year old girl who had various anomalies associated with the syndrome. She sustained a pathological fracture of the left femur at the site of a giant cell tumour. Another lesion occurred in the right fibula, but resolved spontaneously.
戈尔茨综合征是一种罕见病症，其特征为皮肤、牙齿、眼睛和骨骼出现先天性异常。我们报告了一例不寻常的病例，患者为一名17岁女孩，伴有与该综合征相关的多种异常。她左股骨巨细胞瘤部位发生了病理性骨折。右腓骨也出现了另一处病变，但自行消退。
