Swyer Syndrome Presenting as Dysgerminoma: A Case Report

被引：0

作者：

Tarenia, Silima Subhasnigdha ^{[1
]}

Chattopadhyay, Sujaya ^{[2
]}

Das, Niladri ^{[2
,4
]}

Hathi, Deep ^{[2
]}

Baidya, Arjun ^{[2
]}

Chakrborty, Puranjoy ^{[3
]}

Senhupta, Nilanjan ^{[2
]}

Goswami, Soumik ^{[2
]}

机构：

[1] Med Coll & Hosp, Dept Endocrinol, Kolkata, West Bengal, India

[2] Nil Ratan Sircar Med Coll & Hosp, Dept Endocrinol, Kolkata, West Bengal, India

[3] SSKM Hosp, Inst Post Grad Med Educ & Res, Dept Nephrol, Kolkata, West Bengal, India

[4] Nil Ratan Sircar Med Coll & Hosp, Dept Endocrinol, 138, Acharya Jagadish Chandra Bose Rd, Kolkata 700014, West Bengal, India

来源：

JOURNAL OF THE ASEAN FEDERATION OF ENDOCRINE SOCIETIES | 2023年

关键词：

Swyer syndrome; dysgerminoma; amenorrhoea; gonadal dysgenesis; GERM-CELL TUMOR; GONADAL-DYSGENESIS; PATIENT;

D O I：

10.15605/jafes.038.01.15

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Complete gonadal dysgenesis with 46,XY karyotype is a clinical condition characterized by the absence of testicular tissue but with the presence of typical Mullerian 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.

引用

页码：108 / 113

页数：6

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