Kriplani Alka, Savithrisowmya S, Agarwal Nutan, Garg Pradeep, Maheswari Deepa, Ammini A C, Rajan K D Anand
Department of Obstetrics and Gynecology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India.
J Minim Invasive Gynecol. 2009 Jul-Aug;16(4):504-6. doi: 10.1016/j.jmig.2009.04.013.
Androgen insensitivity syndrome is a disorder of sexual differentiation with 46XY karyotype. The gonad is at risk (33% by 50 years of age) for development of malignant tumors. Hence, gonadectomy is warranted. We present a case of a 22-year-old woman diagnosed with androgen insensitivity syndrome during investigation of primary amenorrhea. Ultrasonography showed intraabdominally-located gonads, with a large, nontender cyst of 9.2 x 5.6 x 5.4 cm size, with limited mobility, to the right of the midline. There was also a partial septum, with a wall thickness of 1 to 2 mm and containing clear fluid. Because of suspicion of malignancy, complete surgery including laparoscopic peritoneal cytologic study, gonadectomy, lymphadenectomy, and omentectomy were performed. Histopathologic study showed testis with an epididymal cyst. Formation of epididymal cyst is rare in these cases. The patient did well in the postoperative period. She was put on hormone replacement therapy and is doing well.
雄激素不敏感综合征是一种性分化障碍疾病,核型为46XY。性腺有发生恶性肿瘤的风险(50岁时风险为33%)。因此,有必要进行性腺切除术。我们报告一例22岁女性病例,该患者在原发性闭经检查期间被诊断为雄激素不敏感综合征。超声检查显示性腺位于腹腔内,有一个大小为9.2×5.6×5.4cm的大的、无压痛的囊肿,活动度有限,位于中线右侧。还有一个部分隔膜,壁厚1至2mm,内含清亮液体。由于怀疑为恶性肿瘤,遂进行了包括腹腔镜腹膜细胞学检查、性腺切除术、淋巴结切除术和大网膜切除术在内的完整手术。组织病理学研究显示为睾丸伴附睾囊肿。在这些病例中,附睾囊肿的形成很少见。患者术后恢复良好。她接受了激素替代治疗,情况良好。