Haroon Nisha Nigil, Agarwal Gaurav, Pandey Rakesh, Dabadghao Preeti
Department of Endocrinology, UHN Toronto General Hospital, Toronto, Canada.
Indian J Endocrinol Metab. 2013 Jan;17(1):157-9. doi: 10.4103/2230-8210.107870.
The differential diagnosis for precocious puberty in a young female includes peripheral causes. This case report documents a rare cause of isosexual precocious puberty, a juvenile granulosa cell tumor of the ovary-and a brief literature review. A 7-year-old girl presented with rapid onset of pubertal development and elevated estradiol levels. Abdominal ultrasound revealed a mass in the right adnexa. Other causes of precocious puberty were excluded. Elective surgery was planned, but the patient presented to the emergency room with torsion of ovary. She underwent an exploratory laparotomy for tumor resection and right salpingo oophorectomy. Pathology reported a juvenile granulosa cell tumor of the ovary. Postoperatively, she experienced a cessation of vaginal bleeding and estradiol levels normalized. Early stage disease has good prognosis. Adjuvant chemotherapy is not indicated in this setting.
年轻女性性早熟的鉴别诊断包括外周性病因。本病例报告记录了一种罕见的同性性早熟病因——卵巢幼年型颗粒细胞瘤,并进行简要文献综述。一名7岁女孩出现青春期发育迅速且雌二醇水平升高。腹部超声显示右侧附件有一肿块。排除了其他性早熟病因。计划进行择期手术,但该患者因卵巢扭转被送至急诊室。她接受了剖腹探查术以切除肿瘤并进行右侧输卵管卵巢切除术。病理报告为卵巢幼年型颗粒细胞瘤。术后,她阴道出血停止且雌二醇水平恢复正常。早期疾病预后良好。在此情况下无需辅助化疗。