Moriya A, Futami T, Hashimoto M, Ohara S, Hirao Y, Okajima E, Kita E
Hinyokika Kiyo. 1987 Apr;33(4):609-16.
A case of mixed gonadal dysgenesis with anaplastic seminoma is reported. A 43-year-old, female, who was brought up as a female, was admitted to our hospital for swelling of left inguinal region. The physical examination revealed a short stature, ambiguous external genitalia but no Turner's stigmata. A child's head-sized tumor was noticed in the left inguinal region by CT scan. The histopathological diagnosis of this tumor was anaplastic seminoma. The right gonad was removed at laparotomy with lymph node dissection in the pelvis. Histological examination of right gonad revealed streak gonad and immature uterine with fallopian tube. In the Japanese literature, 7 cases including our case of mixed gonadal dysgenesis with gonadal tumor have been reported.
报告一例混合性性腺发育不全合并间变性精原细胞瘤的病例。一名43岁女性，自幼被当作女性抚养，因左腹股沟区肿胀入住我院。体格检查发现身材矮小，外生殖器模糊，但无特纳氏征。CT扫描显示左腹股沟区有一个儿童头大小的肿瘤。该肿瘤的组织病理学诊断为间变性精原细胞瘤。剖腹手术时切除了右侧性腺，并对盆腔进行了淋巴结清扫。右侧性腺的组织学检查显示为条索状性腺和未成熟子宫及输卵管。在日本文献中，包括我们这例混合性性腺发育不全合并性腺肿瘤的病例在内，共报道了7例。
