Beaulieu Bergeron Mélanie, Lemieux Nicole, Brochu Pierre
Département de Pathologie et biologie cellulaire, Université de Montréal, 2900 boul. Édouard-Montpetit, Montréal, Québec, H3T 1J4, Canada.
Pediatr Dev Pathol. 2011 Nov-Dec;14(6):445-59. doi: 10.2350/11-01-0960-OA.1. Epub 2011 Jun 21.
Patients with XY gonadal dysgenesis are at increased risk of developing gonadal tumors. The etiology of several cases of XY gonadal dysgenesis remains unknown, but X/XY gonadal mosaicism has been hypothesized to play a role. At the histologic level, the presence of persistent primitive sex cords containing immature germ cells in dysgenetic gonads (an entity called undifferentiated gonadal tissue, or UGT) was recently described, and these immature germ cells are thought to be at risk of neoplastic transformation. To further investigate both these aspects, we retrospectively studied the gonads from 30 patients with pure (22) and mixed (8) gonadal dysgenesis. Cytogenetic analyses performed on 35 gonads revealed that structurally abnormal Y chromosomes were lost in a majority of cells from the gonads, explaining the gonadal dysgenesis of patients bearing a rearranged Y chromosome. On the other hand, normal Y chromosomes were less often lost in gonads of patients with gonadal dysgenesis. At the histologic level, 43 of the 51 gonads presented areas characteristic of a streak; 13 of these streak gonads also presented areas of UGT. Structures resembling sex cords but without germ cells were found in many of the streaks not containing UGT, suggesting that UGT was initially present. Of the 13 gonads containing both UGT and a streak, 9 developed a tumor. The proximity of UGT with the tumors as well as the immunostaining patterns (PLAP+, OCT3/4+, and CD117/KIT+) suggests that germ cells found in UGT are a risk factor for gonadal tumors.
XY性腺发育不全患者发生性腺肿瘤的风险增加。几例XY性腺发育不全的病因仍不清楚,但推测X/XY性腺嵌合体可能起作用。在组织学水平上,最近描述了发育异常的性腺中存在含有未成熟生殖细胞的持续原始性索(一种称为未分化性腺组织或UGT的实体),并且这些未成熟生殖细胞被认为有发生肿瘤转化的风险。为了进一步研究这两个方面,我们回顾性研究了30例单纯性(22例)和混合性(8例)性腺发育不全患者的性腺。对35个性腺进行的细胞遗传学分析显示,性腺中的大多数细胞丢失了结构异常的Y染色体,这解释了携带重排Y染色体患者的性腺发育不全。另一方面,性腺发育不全患者的性腺中正常Y染色体较少丢失。在组织学水平上,51个性腺中有43个呈现条索状特征区域;其中13个条索状性腺也呈现UGT区域。在许多不含UGT的条索状结构中发现了类似性索但没有生殖细胞的结构,这表明UGT最初是存在的。在13个同时含有UGT和条索状结构的性腺中,有9个发生了肿瘤。UGT与肿瘤的接近程度以及免疫染色模式(PLAP+、OCT3/4+和CD117/KIT+)表明,UGT中发现的生殖细胞是性腺肿瘤的危险因素。