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继发性生长激素缺乏症在数年中断生长激素替代治疗后发展为肝硬化。

Secondary Growth Hormone Deficiency That Developed into Cirrhosis after Several Years of Interrupted Growth Hormone Replacement Therapy.

作者信息

Sueki Ayana, Kaya Daisuke, Nagamatsu Shinsaku, Yamamoto Chisa, Ohta Kohei, Matsuo Yuya, Nishio Yuya, Komeda Yusuke, Kikukawa Shoma, Matsuura Kyohei, Matsuo Hideki, Uejima Masakazu, Moriya Kei

机构信息

Department of Gastroenterology, Nara Prefecture General Medical Center, Japan.

Department of Endocrinology and Metabolism, Nara Prefecture General Medical Center, Japan.

出版信息

Intern Med. 2025 Feb 1;64(3):387-391. doi: 10.2169/internalmedicine.3896-24. Epub 2024 Jun 27.

DOI:10.2169/internalmedicine.3896-24
PMID:38925969
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11867760/
Abstract

This case report describes a patient who received hormone replacement therapy for secondary panhypopituitarism and subsequently developed diabetes. His physician decided to discontinue growth hormone (GH) replacement, which was previously deemed contraindicated. Following the diagnosis of fatty liver, the patient began to exhibit liver damage that progressed over the ensuing years, ultimately leading to cirrhosis. Common factors linked to cirrhosis were excluded, leading to the belief that GH deficiency over several years was the primary contributor to cirrhosis. Therefore, when treating patients with GH insufficiency and diabetes, clinicians should carefully consider the potential implications of GH replacement therapy.

摘要

本病例报告描述了一名因继发性全垂体功能减退接受激素替代治疗并随后患上糖尿病的患者。他的医生决定停止此前被认为禁忌的生长激素(GH)替代治疗。在诊断出脂肪肝后,患者开始出现肝脏损伤,并在随后几年中逐渐加重,最终发展为肝硬化。排除了与肝硬化相关的常见因素后,认为数年的GH缺乏是肝硬化的主要促成因素。因此,在治疗GH不足和糖尿病患者时,临床医生应仔细考虑GH替代治疗的潜在影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db87/11867760/8438743fa92c/1349-7235-64-0387-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db87/11867760/f148a0ef8540/1349-7235-64-0387-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db87/11867760/269875d0e6c0/1349-7235-64-0387-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db87/11867760/06b6a7bd5fb7/1349-7235-64-0387-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db87/11867760/8438743fa92c/1349-7235-64-0387-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db87/11867760/f148a0ef8540/1349-7235-64-0387-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db87/11867760/269875d0e6c0/1349-7235-64-0387-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db87/11867760/06b6a7bd5fb7/1349-7235-64-0387-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db87/11867760/8438743fa92c/1349-7235-64-0387-g004.jpg

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本文引用的文献

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NAFLD Fibrosis Progression and Type 2 Diabetes: The Hepatic-Metabolic Interplay.非酒精性脂肪性肝病纤维化进展与2型糖尿病:肝脏-代谢相互作用
Life (Basel). 2024 Feb 18;14(2):272. doi: 10.3390/life14020272.
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Genetic and epigenetic determinants of non-alcoholic fatty liver disease (NAFLD) in lean individuals: a systematic review.瘦人非酒精性脂肪性肝病(NAFLD)的遗传和表观遗传决定因素:一项系统综述。
Transl Gastroenterol Hepatol. 2023 Dec 6;9:11. doi: 10.21037/tgh-23-31. eCollection 2024.
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Nonalcoholic fatty liver disease and adult growth hormone deficiency: An under-recognized association?
非酒精性脂肪性肝病与成人生长激素缺乏症:一种被低估的关联?
Best Pract Res Clin Endocrinol Metab. 2023 Dec;37(6):101816. doi: 10.1016/j.beem.2023.101816. Epub 2023 Aug 16.
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MAFLD: an optimal framework for understanding liver cancer phenotypes.MAFLD:理解肝癌表型的最佳框架。
J Gastroenterol. 2023 Oct;58(10):947-964. doi: 10.1007/s00535-023-02021-7. Epub 2023 Jul 20.
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Association of nonalcoholic fatty liver disease and growth hormone deficiency: a systematic review and meta-analysis.非酒精性脂肪性肝病与生长激素缺乏症的相关性:系统评价和荟萃分析。
Endocr J. 2023 Oct 30;70(10):959-967. doi: 10.1507/endocrj.EJ23-0157. Epub 2023 Jul 20.
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Sex, Nutrition, and NAFLD: Relevance of Environmental Pollution.性别、营养与非酒精性脂肪性肝病:环境污染的相关性。
Nutrients. 2023 May 16;15(10):2335. doi: 10.3390/nu15102335.
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Causes and risk profiles of mortality among individuals with nonalcoholic fatty liver disease.非酒精性脂肪性肝病患者死亡的原因和风险概况。
Clin Mol Hepatol. 2023 Feb;29(Suppl):S43-S57. doi: 10.3350/cmh.2022.0351. Epub 2022 Nov 22.
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Endocr Connect. 2021 Feb;10(2):R52-R65. doi: 10.1530/EC-20-0490.
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