ARTICLE
20 October 2025

先天性单侧甲状腺缺如伴对侧癌报告及文献复习

萍艳 李1,2 净渝 杨2 昕 陈2 丹 何1,2 建伟 孙2
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1 昆明理工大学, 中国
2 昆明理工大学附属医院/云南省第一人民医院,乳腺甲状腺外科, 中国
MRP 2025 , 3(10), 114–117; https://doi.org/10.61369/MRP.2025100004
© 2025 by the Author. Licensee Art and Design, USA. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution -Noncommercial 4.0 International License (CC BY-NC 4.0) ( https://creativecommons.org/licenses/by-nc/4.0/ )
Abstract

甲状腺偏侧缺如症是一种先天性疾病,其特征在于甲状腺的部分或完全缺失。近年来,随着分子生物学和遗传学的发展,研究者们在病因探索、临床表现的识别以及治疗方法的改进方面取得了显著进展。然而,甲状腺偏侧缺如症的病理生理过程仍不够清晰,亟待更多的研究来揭示其背后的机制。本文报道了一例左侧先天性甲状腺缺如伴右侧甲状腺乳头状癌的患者,并综述了甲状腺偏侧缺如症的最新研究成果,旨在为临床医生和研究人员提供参考,从而推动该领域的进一步研究与临床应用。

Keywords
甲状腺偏侧缺如症
发病机制
遗传学
References

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