Le Gall C, Bouvier R, Chappuis J P, Hermier M
Unité de Gastroentérologie et Nutrition Pédiatrique, Hôpital E.-Herriot, Lyon.
Arch Fr Pediatr. 1991 Feb;48(2):115-8.
The authors report one case of Ollier's disease in a 12 year-old girl in whom the occurrence of an ascites revealed a secretant juvenile granulosa cell tumor some years later. The tumor was right-sided, homolateral to the hemicorporal side involved by enchondromatosis. Five other cases of this association were previously reported. Attention is drawn not only to the risk of chondrosarcomatous change but also to the possible recurrence of ovarian tumor in the year following ovariectomy.
作者报告了一例12岁女孩的Ollier病，该女孩数年后出现腹水，提示存在分泌性幼年型颗粒细胞瘤。肿瘤位于右侧，与内生软骨瘤病累及的半侧身体同侧。此前曾报告过另外5例这种关联病例。不仅要注意软骨肉瘤变的风险，还要注意卵巢切除术后一年内卵巢肿瘤可能复发的情况。
