Fayez J A, Jonas H S
Obstet Gynecol. 1978 Oct;52(4):490-2.
A case of gonadal dysgenesis in a phenotypic female associated with neoplastic changes is presented. The patient typified a classic case of Turner syndrome with a 45, XO chromosomal compliment, becoming virilized as a result of the development of bilateral hilar cell hyperplasia in her dysgenetic gonads. The malignant potential of the dysgenetic gonad is stressed in this report. Early diagnosis and appropriate management are emphasized as the two factors that make the difference in the outcome of the patient with gonadal dysgenesis.
本文报告了一例伴有肿瘤性改变的表型女性性腺发育不全病例。该患者是典型的特纳综合征病例,染色体核型为45,XO,其发育不全的性腺中双侧门细胞增生,导致患者男性化。本报告强调了发育不全性腺的恶性潜能。早期诊断和适当治疗是影响性腺发育不全患者预后的两个关键因素,对此予以了强调。