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一名核型为46, XY的真两性畸形(性分化障碍)患者患有双侧性腺母细胞瘤,左侧为无性细胞瘤。

Bilateral gonadoblastomas with a left sided dysgerminoma in a true hermaphrodite (disorder of sexual differentiation) with 46, XY karyotype.

作者信息

Kini Usha, Bantwal G, Ayyar V, Idiculla Jyothi

机构信息

Department of Pathology, St. John's Medical College and Hospital, Bangalore, India.

出版信息

J Assoc Physicians India. 2008 Jul;56:549-51.

Abstract

Ovotesticular DSD is not an uncommon disorder. The presence of Y chromosome confers a high risk of neoplastic transformation in dysgenetic gonads. The neoplastic development in these patients is associated with the presence of Y chromosome and intra abdominal location of the abnormal gonad. We report histogenetic details of a rare occurrence of bilateral gonadoblastomas and left sided dysgerminoma in a XY ovotestes DSD (disorder of sexual differentiation) in an 18 year old with a female phenotype.

摘要

卵睾性发育障碍并非罕见疾病。Y染色体的存在使发育异常的性腺发生肿瘤转化的风险很高。这些患者的肿瘤发生与Y染色体的存在以及异常性腺位于腹腔内有关。我们报告了一名18岁女性表型的XY卵睾性发育障碍(性分化障碍)患者罕见地发生双侧生殖细胞瘤和左侧无性细胞瘤的组织发生学细节。

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