Rasalkar Darshana D, Paunipagar Bhawan K, Ng Alex, Lai Fernand M, Bagaria Shalini Jain
Department of Imaging and Interventional Radiology, Prince of Wales Hospital, The Chinese University of Hong Kong, Ngan Shing Street, Shatin, New Territories, Hong Kong.
Case Rep Radiol. 2011;2011:592124. doi: 10.1155/2011/592124. Epub 2011 Aug 28.
We report a case of intra-abdominal testicular tumor in a 36-year-old married lady presenting with chief complaints of primary amenorrhea. The patient was later diagnosed with testicular feminization syndrome, a form of male pseudohermaphroditism. This testicular tumor was histologically proven as seminoma. Due to rarity, imaging findings in patients with testicular feminization syndrome and intraabdominal testicular tumor have been poorly documented. So far, only one case report had described the combined role of CT and MR imaging in intraabdominal testicular sex-cord stromal tumor. To our knowledge, this case is first to document USG and MR imaging in addition to MR spectroscopy features in intraabdominal testicular seminoma.
我们报告一例36岁已婚女性的腹腔内睾丸肿瘤病例,其主要症状为原发性闭经。该患者后来被诊断为睾丸女性化综合征,这是一种男性假两性畸形。此睾丸肿瘤经组织学证实为精原细胞瘤。由于病例罕见,关于睾丸女性化综合征合并腹腔内睾丸肿瘤患者的影像学表现记录甚少。到目前为止,仅有一篇病例报告描述了CT和MR成像在腹腔内睾丸性索间质肿瘤中的联合作用。据我们所知,本病例首次记录了腹腔内睾丸精原细胞瘤的超声检查(USG)、MR成像以及磁共振波谱特征。