Nagai Tamiko, Hasegawa Kiyoshi, Motegi Emi, Machida Hiromi, Sasaki Hideo, Kato Hikaru, Kosaka Nobuaki, Fukasawa Ichio, Kuroda Hajime
Department of Pathology, Dokkyo Medical University.
Department of Obstetrics and Gynecology, Dokkyo Medical University.
Diagn Cytopathol. 2019 Nov;47(11):1203-1207. doi: 10.1002/dc.24282. Epub 2019 Jul 23.
Ovarian gonadoblastoma coexisting with a dysgerminoma is extremely rare in patients with Turner syndrome (TS) and a Y chromosome. The cytological findings, including imprint cytology, of these unusual ovarian tumors have rarely been reported. We report a rare patient with a gonadoblastoma with dysgerminoma, 3.0 × 2.0 cm in size; she was a 19-year-old woman with TS and a Y chromosome. She underwent laparoscopic bilateral gonadectomy, and the tumor was classified as stage IA (pT1aNxM0) according to the International Federation of Gynecology and Obstetrics classification system. Intraoperative imprint cytology revealed two types of neoplastic cells: small tumor cells surrounding light green-stained or eosinophilic hyaline globules with marked calcification, suspicious for gonadoblastoma; and large, round, atypical cells with abundant cytoplasm, macronucleoli, and marked lymphocytic infiltration (two-cell pattern), suspicious for dysgerminoma. The cytology results in our patient may represent the second reported results of imprint cytology describing a gonadoblastoma with dysgerminoma. They are the first reported results in a patient with TS and a Y chromosome.
在患有特纳综合征(TS)且有Y染色体的患者中,卵巢性腺母细胞瘤与无性细胞瘤共存极为罕见。这些不寻常的卵巢肿瘤的细胞学检查结果,包括印片细胞学检查结果,鲜有报道。我们报告了一例罕见的性腺母细胞瘤合并无性细胞瘤患者,肿瘤大小为3.0×2.0 cm;患者为一名19岁患有TS且有Y染色体的女性。她接受了腹腔镜双侧性腺切除术,根据国际妇产科联盟分类系统,该肿瘤被分类为IA期(pT1aNxM0)。术中印片细胞学检查发现两种类型的肿瘤细胞:围绕着浅绿色染色或嗜酸性透明小球且有明显钙化的小肿瘤细胞,怀疑为性腺母细胞瘤;以及大的、圆形的、非典型细胞,胞质丰富,有大核仁,且有明显的淋巴细胞浸润(双细胞模式),怀疑为无性细胞瘤。我们患者的细胞学检查结果可能是第二例报道的描述性腺母细胞瘤合并无性细胞瘤的印片细胞学检查结果。它们是首例报道的患有TS且有Y染色体患者的检查结果。