Cronjé H S, Niemand I, Bam R H, Woodruff J D
Department of Gynecology and Obstetrics, Johns Hopkins Hospital, Baltimore, Maryland, USA.
Obstet Gynecol Surv. 1998 Apr;53(4):240-7. doi: 10.1097/00006254-199804000-00022.
The files of the Emil Novak Ovarian Tumor Registry (ENOTR) were searched for granulosa and theca cell tumors in children aged 12 years and less. In addition, an extensive literature search was done for English publications on children with these tumors aged 10 years or less. Of the 17 children from the ENOTR, 5 had adult-type granulosa cell tumors, 6 had juvenile granulosa cell tumors, and 1 had a luteinized granulosa cell tumor. In addition, there were three cases with gonadal stomal tumors, one theca cell tumor, and one granulosa-theca cell tumor. Precocious pseudopuberty was present in 70 percent of the children, abdominal pain in 24 percent, and ascites in 18 percent. The literature review revealed a tumor-related mortality rate of 9 percent (based on 163 cases with granulosa cell tumors, including the juvenile type). Some of these tumors are large with acute pain, but nevertheless, the prognosis is good, particularly in cases with precocious puberty. Treatment can be conservative.
在埃米尔·诺瓦克卵巢肿瘤登记处(ENOTR)的档案中,查找12岁及以下儿童的颗粒细胞瘤和卵泡膜细胞瘤。此外,还对关于10岁及以下患有这些肿瘤儿童的英文出版物进行了广泛的文献检索。在ENOTR的17名儿童中,5例患有成人型颗粒细胞瘤,6例患有青少年型颗粒细胞瘤,1例患有黄素化颗粒细胞瘤。此外,还有3例性腺间质肿瘤、1例卵泡膜细胞瘤和1例颗粒-卵泡膜细胞瘤。70%的儿童出现性早熟假性青春期,24%出现腹痛,18%出现腹水。文献综述显示肿瘤相关死亡率为9%(基于163例颗粒细胞瘤病例,包括青少年型)。其中一些肿瘤体积较大且伴有急性疼痛,但尽管如此,预后良好,尤其是性早熟的病例。治疗可以是保守的。