Moyles K, Chan Y F, Hamill J, Massey R
Histopathology Laboratory and Paediatric Surgery, Auckland, New Zealand.
Pathology. 1995 Oct;27(4):371-3. doi: 10.1080/00313029500169343.
Sertoli-Leydig cell tumors (SLCT) are sex cord-stromal tumors which exhibit testicular differentiation.1 They account for less than 0.2% of ovarian neoplasms in total but comprise 4% of ovarian tumors in females under 20 yrs of age.2 The morphological appearance of these tumors varies more widely than that of any other ovarian tumor except for the teratomas. Histologically they are now classified into 5 categories: well-differentiated, intermediately differentiated, poorly differentiated, heterologous and retiform.1 We describe the case of an ovarian Sertoli-Leydig cell tumor with retiform pattern in a 7 yr old girl.
支持细胞-间质细胞瘤(SLCT)是具有睾丸分化特征的性索间质肿瘤。1它们在所有卵巢肿瘤中占比不到0.2%,但在20岁以下女性的卵巢肿瘤中占4%。2这些肿瘤的形态外观比除畸胎瘤外的任何其他卵巢肿瘤变化更大。从组织学上看,它们现在被分为5类:高分化、中分化、低分化、异源性和网状型。1我们描述了一名7岁女孩患有网状型卵巢支持细胞-间质细胞瘤的病例。