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青少年原发性甲状腺功能减退继发垂体增生：一例医学病例报告及文献综述

Pituitary hyperplasia secondary to primary hypothyroidism in adolescents: A medical case report and literature review.

作者信息

Yuan Xiangfeng, Zhu Jiangyu, Su Xiaoyu, Tan Huiling, Wang Siqi, Zheng Xueying, Ding Yu, Li Sumei

机构信息

Division of Life Sciences and Medicine, Department of Endocrinology, The First Affiliated Hospital of USTC University of Science and Technology of China Hefei Anhui China.

Department of Endocrinology, Funan Hospital of Traditional Chinese Medicine Fuyang Anhui China.

出版信息

Clin Case Rep. 2024 Nov 5;12(11):e9541. doi: 10.1002/ccr3.9541. eCollection 2024 Nov.

DOI:10.1002/ccr3.9541
PMID:39502127
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11535441/
Abstract

Prompt and precise diagnosis of pituitary hyperplasia secondary to primary hypothyroidism (PHPH) is crucial to avoid unwarranted pituitary surgery and potential permanent impairment. Although PHPH may present similarly to pituitary adenoma, it is responsive to thyroxine therapy, underscoring the critical role of differential diagnosis in the treatment of adolescent patients.

摘要

对原发性甲状腺功能减退继发垂体增生（PHPH）进行及时、准确的诊断对于避免不必要的垂体手术及潜在的永久性损害至关重要。尽管PHPH的表现可能与垂体腺瘤相似，但它对甲状腺素治疗有反应，这凸显了鉴别诊断在青少年患者治疗中的关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e92/11535441/fae66e379462/CCR3-12-e9541-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e92/11535441/fae66e379462/CCR3-12-e9541-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e92/11535441/fae66e379462/CCR3-12-e9541-g001.jpg

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J Assoc Physicians India. 2022 Jan;70(1):11-12.
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Primary hypothyroidism with pituitary hyperplasia characterized by hypogonadotropic hypogonadism: a case report and review of the literature.以低促性腺激素性性腺功能减退为特征的原发性甲状腺功能减退伴垂体增生：一例报告并文献复习
Ann Palliat Med. 2020 Nov;9(6):4359-4370. doi: 10.21037/apm-20-1828. Epub 2020 Nov 10.
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Trop Doct. 2020 Jul;50(3):240-242. doi: 10.1177/0049475520907421. Epub 2020 Feb 27.
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