Ozsu Elif, Mutlu Gul Yesiltepe, Cizmecioglu Filiz M, Ekingen Gülsen, Muezzinoglu Bahar, Hatun Sukru
J Pediatr Endocrinol Metab. 2013;26(7-8):789-91. doi: 10.1515/jpem-2012-0386.
Ovotesticular disorder of sexual development (DSD) is characterized by the presence of both ovarian and testicular tissues in the same individual. The most common karyotype is 46,XX. Here, we report the case of a boy with a 46,XX/47,XXY karyotype diagnosed as ovotesticular DSD by gonadal biopsy. A 5-month-old boy presented with hypospadias, unilateral cryptorchidism, and a micropenis. Pelvic magnetic resonance imaging revealed a suspicious gonad tissue that is solid in structure in the right scrotum and a suspicious gonad that is cystic in structure in the left inguinal canal. He underwent a diagnostic laparoscopy. Cytogenetic analysis of peripheral blood revealed a 46,XX/47,XXY karyotype. Histopathologic examination of the left gonad showed ovarian tissue containing primordial follicles with ipsilateral undifferentiated tuba uterina. The right gonad showed immature testis tissue. He underwent left gonadectomy and hypospadias repair, and was raised as a male. Through this rare case, we highlight the importance of histological and cytogenetic investigation in DSD.
卵睾性发育障碍(DSD)的特征是同一个体同时存在卵巢和睾丸组织。最常见的核型是46,XX。在此,我们报告一例核型为46,XX/47,XXY的男孩,经性腺活检诊断为卵睾性DSD。一名5个月大的男孩出现尿道下裂、单侧隐睾和小阴茎。盆腔磁共振成像显示右侧阴囊内有一个结构实性的可疑性腺组织,左侧腹股沟管内有一个结构囊性的可疑性腺。他接受了诊断性腹腔镜检查。外周血细胞遗传学分析显示核型为46,XX/47,XXY。左侧性腺的组织病理学检查显示卵巢组织含有原始卵泡,同侧有未分化的输卵管。右侧性腺显示为未成熟睾丸组织。他接受了左侧性腺切除术和尿道下裂修复术,并作为男性抚养。通过这个罕见病例,我们强调了组织学和细胞遗传学检查在DSD中的重要性。