From the Division of Gynecologic Oncology, University of Minnesota Department of Obstetrics, Gynecology and Women's Health, Minneapolis, Minnesota.
Obstet Gynecol. 2010 Aug;116 Suppl 2:550-552. doi: 10.1097/AOG.0b013e3181e4bfe9.
Gonadal dysgenesis encompasses a variety of sexual differentiation disorders. Within this population of patients, there is an increased risk of gonadal tumor formation.
In this case series of three patients, two with Swyer's syndrome (complete gonadal dysgenesis) and one with mosaic Turner's syndrome, three separate histologic subtypes of tumors were identified: dysgerminoma, seminoma, and gonadoblastoma. The patients with dysgerminoma and seminoma had regular menses and were without recurrent disease. We recommend that the patient with gonadoblastoma start on hormone therapy.
Once the diagnosis of gonadal dysgenesis is made, prophylactic gonadectomy should be performed owing to the probability of malignant transformation. These patients illustrate the potential different presentations with gonadal dysgenesis and the importance of complete evaluation of patients with primary amenorrhea.
性腺发育不全包括多种性分化障碍。在这群患者中,存在性腺肿瘤形成的风险增加。
在这个由三例患者组成的病例系列中,两例为斯韦尔综合征(完全性腺发育不全),一例为特纳综合征嵌合体,三种不同的组织学肿瘤亚型被确定:生殖细胞瘤、精原细胞瘤和性腺母细胞瘤。患有生殖细胞瘤和精原细胞瘤的患者月经正常,且无疾病复发。我们建议患有性腺母细胞瘤的患者开始激素治疗。
一旦做出性腺发育不全的诊断,由于恶性转化的可能性,应进行预防性性腺切除术。这些患者说明了性腺发育不全的潜在不同表现,以及对原发性闭经患者进行全面评估的重要性。