Gell J S, Stannard M W, Ramnani D M, Bradshaw K D
Department of Obstetrics and Gynecology, University of Texas Southwestern Medical Center at Dallas, Texas 75235-9032, USA.
J Pediatr Adolesc Gynecol. 1998 Aug;11(3):147-50. doi: 10.1016/s1083-3188(98)70135-4.
Juvenile granulosa cell tumor (JGCT) of the ovary has been reported to occur rarely in conjunction with Ollier's disease. We report a case of a 13-year-old girl who was noted to have a large abdominal mass at the time of excision of a symptomatic enchondroma of the right femur. Subsequent laparotomy at a tertiary care children's medical center identified a JGCT confined to the right ovary. Review of the literature reveals eight previous cases of JGCT in patients with Ollier's disease. The pathophysiology and possible common causes of both disorders is discussed.
据报道，卵巢幼年型颗粒细胞瘤（JGCT）很少与Ollier病同时发生。我们报告一例13岁女孩，在切除右股骨有症状的内生软骨瘤时发现腹部有一巨大肿块。随后在一家三级儿童医疗中心进行剖腹手术，发现一个局限于右卵巢的JGCT。文献回顾显示，之前有8例Ollier病患者发生JGCT的病例。本文讨论了这两种疾病的病理生理学及可能的共同病因。
