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一例甲状腺半侧发育不全伴双异位甲状腺组织。

A case of hemiagenesis of thyroid with double ectopic thyroid tissue.

作者信息

Velayutham Kumaravel, Mahadevan Shriraam, Velayutham Latha, Jayapaul Muthukumaran, Appakalai Balamurugan, Kannan Arun

机构信息

Alpha Hospital and Research Center, Madurai, India.

出版信息

Indian J Endocrinol Metab. 2013 Jul;17(4):756-8. doi: 10.4103/2230-8210.113777.

Abstract

Developmental abnormalities of the thyroid gland are very rare. The most common abnormalities include ectopic thyroid tissues that are commonly seen in lingual or sublingual location, agenesis, and hemiagenesis of the thyroid gland. These developmental defects may or may not be associated with thyroid dysfunction. Our case is an 18-year-old male who presented with swelling in the neck of 4-year duration. Clinical examination revealed an oval-shape swelling in the left side of the thyroid gland. The ultrasound and the nuclear scan report revealed the presence of thyroid hemiagenesis of the right lobe with isthmus along with double ectopic thyroid tissue at suprahyoid and infrahyoid region. His thyroid function test showed elevated thyroid-stimulating hormone (TSH) and normal free T4. We report a very rare case of thyroid hemiagenesis with double ectopic thyroid tissue; and to the best of our knowledge, this is the first report in the world literature.

摘要

甲状腺发育异常非常罕见。最常见的异常包括异位甲状腺组织,常见于舌部或舌下位置,甲状腺缺如和半侧发育不全。这些发育缺陷可能与甲状腺功能障碍有关,也可能无关。我们的病例是一名18岁男性,颈部肿胀4年。临床检查发现甲状腺左侧有椭圆形肿胀。超声和核扫描报告显示右叶甲状腺半侧发育不全伴峡部,以及舌骨上和舌骨下区域的双异位甲状腺组织。他的甲状腺功能测试显示促甲状腺激素(TSH)升高,游离T4正常。我们报告了一例非常罕见的甲状腺半侧发育不全伴双异位甲状腺组织的病例;据我们所知,这是世界文献中的首例报告。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f68b/3743386/86a698661c18/IJEM-17-756-g001.jpg

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