A case of Mayer-Rokitansky-Kuster-Hauser syndrome presenting as Graves disease

被引：0

作者：

Lim, Ye-Jee ^{[2
]}

Sohn, Tae-Seo ^{[1
,2
]}

Kang, Seung-Hun ^{[2
]}

Chang, Kyung-Yoon ^{[2
]}

Kim, Bo-Kyung ^{[2
]}

Kim, Yeon-Ji ^{[2
]}

Ha, Won-Chul ^{[2
]}

Oh, Su-Jin ^{[2
]}

Son, Hyun-Shik ^{[2
]}

机构：

[1] Uijeongbu St Marys Hosp, Dept Internal Med, Uijeongbu Si 480717, Gyeonggi Do, South Korea

[2] Catholic Univ Korea, Dept Internal Med, Seoul, South Korea

来源：

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM | 2012年 / 25卷 / 11-12期

关键词：

Mayer-Rokitansky-Kuster-Hauser syndrome; Mullerian aplasia; primary amenorrhea; thyrotoxicosis; MENSTRUAL DISTURBANCES; THYROID-DISEASE; MANAGEMENT;

D O I：

10.1515/jpem-2012-0084

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

The Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a congenital disorder characterized by aplasia of the uterus and the upper part of the vagina in an XX individual with normal development of secondary sexual characteristics. Individuals with this syndrome may also present with renal and skeletal abnormalities. We report a case of a 16-year-old girl presenting with thyrotoxicosis and primary amenorrhea. After being diagnosed with Graves disease, this patient was placed on antithyroid medication. Although her thyroid function normalized, she did not start to menstruate. Therefore, we assessed her primary amenorrhea and diagnosed the patient with MRKH syndrome through pelvic imaging. To our knowledge, an association between Graves disease and MRKH syndrome has not yet been reported.

引用

页码：1169 / 1171

页数：3

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