Swyer Syndrome Presenting as Dysgerminoma: A Case Report.

IF 0.6 Q4 ENDOCRINOLOGY & METABOLISM

Journal of the ASEAN Federation of Endocrine Societies Pub Date : 2023-01-01 DOI:10.15605/jafes.038.01.15

Silima Subhasnigdha Tarenia, Sujaya Chattopadhyay, Niladri Das, Deep Hathi, Arjun Baidya, Puranjoy Chakrabarty, Nilanjan Sengupta, Soumik Goswami

引用次数: 0

Abstract

Complete gonadal dysgenesis with 46,XY karyotype is a clinical condition characterized by the absence of testicular tissue but with the presence of typical Müllerian structures in a phenotypically female individual. The condition presents as primary amenorrhoea or delayed puberty. Eventually, malignant neoplasms may arise. We report a case of a 16-year-old Indian male with Swyer syndrome presenting with primary amenorrhoea and with an earlier diagnosis of a malignant dysgerminoma in the right ovary.

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以生殖细胞异常瘤为表现的Swyer综合征1例报告。

46,XY核型的完全性腺发育不良是一种临床症状，其特征是睾丸组织缺失，但存在典型的勒氏体结构。病情表现为原发性闭经或青春期延迟。最终，可能出现恶性肿瘤。我们报告一例16岁的印度男性与斯威耶综合征表现为原发性闭经和早期诊断的恶性生殖细胞异常瘤在右卵巢。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Journal of the ASEAN Federation of Endocrine Societies ENDOCRINOLOGY & METABOLISM-

CiteScore

1.20

自引率

0.00%

发文量

审稿时长

8 weeks

期刊介绍： The Journal of the ASEAN Federation of Endocrine Societies (JAFES) is an OPEN ACCESS, internationally peer-reviewed, English language, medical and health science journal that is published in print two times a year by the ASEAN Federation of Endocrine Societies. It shall serve as the endocrine window between the ASEAN region and the world, featuring original papers and publishing key findings from specialists and experts of endocrinology.