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希恩综合征:一种针对隐匿性疾病的当前治疗方法。

Sheehan syndrome: a current approach to a dormant disease.

作者信息

Karaca Zuleyha, Kelestimur Fahrettin

机构信息

Department of Endocrinology and Metabolism, Faculty of Medicine, Erciyes University, Kayseri, Türkiye.

Department of Endocrinology and Metabolism, Faculty of Medicine, Yeditepe University, Istanbul, Türkiye.

出版信息

Pituitary. 2025 Jan 25;28(1):20. doi: 10.1007/s11102-024-01481-1.

DOI:10.1007/s11102-024-01481-1
PMID:39863703
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11762620/
Abstract

Sheehan syndrome (SS) is postpartum pituitary necrosis leading to severe hypopituitarism. Severe bleeding during delivery and postpartum period results in ischemic necrosis of the enlarged pituitary gland during pregnancy. The improved obstetrical care decreased the incidence of SS significantly, however SS should always be kept in mind in the etiologies of hypopitutarism in women which can be easily recognized by medical history of the patient. The nonspecific signs and symptoms of hypopituitarism result in significant delay in diagnosis and treatment. The diagnostic delay makes the patients to expose hypopituitarism without essential replacement therapies leading to increased morbidity and mortality of the patients. Awareness of physicians about SS is critical for the diagnosis of the disease. In this review, the epidemiology, pathophysiology, clinical manifestations and treatment of SS are discussed in the light of recent studies.

摘要

希恩综合征(SS)是产后垂体坏死导致的严重垂体功能减退。分娩期及产后期的严重出血会导致孕期增大的垂体发生缺血性坏死。产科护理的改善显著降低了希恩综合征的发病率,然而在女性垂体功能减退的病因中,希恩综合征仍应始终被考虑在内,通过患者病史通常很容易识别。垂体功能减退的非特异性体征和症状导致诊断和治疗出现显著延迟。诊断延迟使患者在未接受必要替代治疗的情况下暴露于垂体功能减退状态,从而导致患者发病率和死亡率增加。医生对希恩综合征的认识对于该疾病的诊断至关重要。在这篇综述中,将根据近期研究对希恩综合征的流行病学、病理生理学、临床表现及治疗进行讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2322/11762620/15d12ce2699a/11102_2024_1481_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2322/11762620/80908776c97a/11102_2024_1481_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2322/11762620/15d12ce2699a/11102_2024_1481_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2322/11762620/80908776c97a/11102_2024_1481_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2322/11762620/15d12ce2699a/11102_2024_1481_Fig2_HTML.jpg

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Sheehan's Syndrome in a Patient With Factor XI Deficiency.一名患有因子XI缺乏症患者的席汉综合征
Cureus. 2024 Jun 13;16(6):e62328. doi: 10.7759/cureus.62328. eCollection 2024 Jun.
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The diagnosis and prevalence of hypoprolactinemia in patients with panhypopituitarism and the effects on depression and sexual functions.垂体功能减退症患者低催乳素血症的诊断和患病率,及其对抑郁和性功能的影响。
Pituitary. 2024 Jun;27(3):277-286. doi: 10.1007/s11102-024-01393-0. Epub 2024 May 3.
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Bone mineral density, turnover, and microarchitecture assessed by second-generation high-resolution peripheral quantitative computed tomography in patients with Sheehan's syndrome.应用第二代高分辨率外周定量计算机断层扫描评估席汉氏综合征患者的骨矿物质密度、转换率和微观结构。
Osteoporos Int. 2024 May;35(5):919-927. doi: 10.1007/s00198-024-07062-z. Epub 2024 Mar 20.
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Androgen deficiency in hypopituitary women: its consequences and management.垂体功能减退女性的雄激素缺乏:其后果和管理。
Rev Endocr Metab Disord. 2024 Jun;25(3):479-488. doi: 10.1007/s11154-024-09873-1. Epub 2024 Jan 19.
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Rev Endocr Metab Disord. 2024 Jun;25(3):505-512. doi: 10.1007/s11154-023-09869-3. Epub 2023 Dec 26.
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Sella Turcica Size in Women with Sheehan Syndrome-A Case-Control Study.希恩综合征女性患者的蝶鞍大小——一项病例对照研究
Indian J Endocrinol Metab. 2023 Sep-Oct;27(5):431-435. doi: 10.4103/ijem.ijem_316_22. Epub 2023 Jun 30.
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Clinical Significance of Procalcitonin, Lactic Acid, and Endotoxin Testing for Children With Severe Pneumonia and Sepsis.降钙素原、乳酸及内毒素检测对儿童重症肺炎合并脓毒症的临床意义
Altern Ther Health Med. 2023 Apr;29(3):218-223.
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High prevalence of coronary artery calcification and increased risk for coronary artery disease in patients with Sheehan syndrome-A case-control study.希恩综合征患者冠状动脉钙化的高患病率及冠状动脉疾病风险增加——一项病例对照研究
Clin Endocrinol (Oxf). 2023 Mar;98(3):375-382. doi: 10.1111/cen.14871. Epub 2022 Dec 30.
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