Washington Hospital Center, Washington, DC 20010, USA.
Fertil Steril. 2011 Jun;95(7):2430.e7-9. doi: 10.1016/j.fertnstert.2011.03.068. Epub 2011 Apr 15.
To describe a rare case of 45,X Turner's syndrome with elevated T and clitoromegaly caused by ovarian hilus cell hyperplasia.
Case report.
Tertiary care pediatric hospital.
PATIENT(S): An 11-and-a-half-year-old girl with 45,X karyotype showed signs of accelerated growth and clitoromegaly and was found to have elevated serum T. Fluorescence in situ hybridization was used to confirm her karyotype as monosomy X and absence of the SRY gene. Elevated gonadotropins indicated absence of ovarian function.
INTERVENTION(S): Laparoscopic bilateral gonadectomy.
MAIN OUTCOME MEASURE(S): Serum T level.
RESULT(S): Pathology showed ovarian hilus cell hyperplasia within the removed gonads. Serum T levels returned to normal after gonadectomy.
CONCLUSION(S): Ovarian hilus cell hyperplasia is an extremely rare cause of virilization in Turner's syndrome. Gonadectomy should be considered for patients with confirmed 45,X karyotype who exhibit virilization.
描述一例罕见的 45,X 特纳综合征病例,其特征为血清 T 升高和阴蒂肥大,病因是卵巢门细胞增生。
病例报告。
三级儿科医院。
一名 11 岁半的女孩,核型为 45,X,表现出生长加速和阴蒂肥大的迹象,且血清 T 升高。荧光原位杂交用于确认其核型为单体 X 和 SRY 基因缺失。升高的促性腺激素提示卵巢功能缺失。
腹腔镜双侧性腺切除术。
血清 T 水平。
切除的性腺的病理显示卵巢门细胞增生。性腺切除术后,血清 T 水平恢复正常。
卵巢门细胞增生是特纳综合征患者性发育异常的罕见原因。对于表现出性发育异常的确诊为 45,X 核型的患者,应考虑行性腺切除术。