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本文引用的文献

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Int J Surg Case Rep. 2021 Sep;86:106372. doi: 10.1016/j.ijscr.2021.106372. Epub 2021 Sep 7.
2
Thyroid hemiagenesis with a TI-RADS 2 nodule in the contralateral lobe.甲状腺半侧缺如,对侧叶有一个TI-RADS 2类结节。
Thyroid Res. 2021 Apr 30;14(1):10. doi: 10.1186/s13044-021-00101-5.
3
Hemiagenesis of the thyroid gland detected by coincidence-what is the clinical relevance? : Case report and review of the literature.巧合发现的甲状腺半侧发育不全:临床意义是什么?病例报告及文献综述
Wien Med Wochenschr. 2020 Nov;170(15-16):403-409. doi: 10.1007/s10354-020-00783-w. Epub 2020 Oct 7.
4
Toxic Adenoma in a Patient with Thyroid Hemiagenesis.甲状腺半侧发育不全患者的毒性腺瘤
Cureus. 2017 Sep 17;9(9):e1695. doi: 10.7759/cureus.1695.
5
Prevalence and Characterization of Thyroid Hemiagenesis in Japan: The Fukushima Health Management Survey.日本甲状腺半侧发育不全的流行情况及特征:福岛健康管理调查。
Thyroid. 2017 Aug;27(8):1011-1016. doi: 10.1089/thy.2016.0662.
6
Thyroid hemiagenesis, Graves' disease and differentiated thyroid cancer: a very rare association: case report and review of literature.甲状腺半侧发育不全、格雷夫斯病与分化型甲状腺癌:一种极为罕见的关联:病例报告及文献综述
Hormones (Athens). 2015 Jul-Sep;14(3):451-8. doi: 10.14310/horm.2002.1606.
7
Congenital thyroid hemiagenesis with multinodular goiter.先天性甲状腺半侧缺如伴结节性甲状腺肿
Acta Radiol Short Rep. 2014 Sep 30;3(9):2047981614530286. doi: 10.1177/2047981614530286. eCollection 2014 Oct.
8
Bilobar thyroid agenesis with primary hyperparathyroidism: report of a case.双侧叶甲状腺缺如伴原发性甲状旁腺功能亢进症:1例报告
Surg Today. 2015 Jun;45(6):787-92. doi: 10.1007/s00595-014-0990-5. Epub 2014 Aug 6.
9
A case of hemiagenesis of thyroid with double ectopic thyroid tissue.一例甲状腺半侧发育不全伴双异位甲状腺组织。
Indian J Endocrinol Metab. 2013 Jul;17(4):756-8. doi: 10.4103/2230-8210.113777.
10
Rare developmental abnormalities of thyroid gland, especially multiple ectopia: A review and our experience.甲状腺罕见的发育异常,尤其是多发性异位:综述及我们的经验
Indian J Nucl Med. 2010 Oct;25(4):143-6. doi: 10.4103/0972-3919.78248.

胶体结节性甲状腺肿合并甲状腺半侧发育不全。

Colloid nodular goitre associated with hemiagenesis of the thyroid gland.

机构信息

Department of Surgery, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India.

Department of Surgery, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India

出版信息

BMJ Case Rep. 2024 Jan 9;17(1):e253843. doi: 10.1136/bcr-2022-253843.

DOI:10.1136/bcr-2022-253843
PMID:38199663
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10806960/
Abstract

Hemiagenesis of the thyroid gland is a rare congenital abnormality usually left unnoticed without associated thyroid disorders. The most common congenital anomaly of the thyroid gland is a thyroglossal cyst, followed by ectopic thyroid tissue and thyroid dysgenesis, which may be agenesis or hemiagenesis. Preoperative underevaluation of the thyroid hemiagenesis (THA) associated with other thyroid disorders may cause intraoperative difficulty in identifying the gland and difficulty in preservation or even identification of major neurovascular structures during neck exploration. We report a patient who presented to us with right-sided neck swelling. On further evaluation and neck exploration, the patient was diagnosed with THA of the left lobe with right colloid goitre.

摘要

甲状腺半侧发育不全是一种罕见的先天性异常,通常无相关甲状腺疾病而不被察觉。甲状腺最常见的先天性异常是甲状舌管囊肿,其次是异位甲状腺组织和甲状腺发育不良,可能是发育不全或半侧发育不全。术前对伴发其他甲状腺疾病的甲状腺半侧发育不全(THA)评估不足,可能导致术中识别该腺体困难,在颈部探查过程中难以保留甚至识别主要的神经血管结构。我们报告了 1 例以右侧颈部肿胀就诊的患者。进一步评估和颈部探查后,患者被诊断为左侧甲状腺半叶发育不全合并右侧胶质性甲状腺肿。