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本文引用的文献

1
Long-term hepatic and cardiac health in patients diagnosed with Sheehan's syndrome.希恩氏综合征患者的长期肝脏和心脏健康。
Pituitary. 2022 Dec;25(6):971-981. doi: 10.1007/s11102-022-01282-4. Epub 2022 Oct 15.
2
Hormone Immunoassay Interference: A 2021 Update.激素免疫测定干扰:2021 更新版。
Ann Lab Med. 2022 Jan 1;42(1):3-23. doi: 10.3343/alm.2022.42.1.3.
3
Hormones and the bone marrow: panhypopituitarism and pancytopenia in a man with a pituitary adenoma.激素与骨髓:一名垂体腺瘤男性患者的全垂体功能减退和全血细胞减少症
J Gen Intern Med. 2015 May;30(5):692-6. doi: 10.1007/s11606-014-3161-x.
4
Sheehan's syndrome: Newer advances.希恩综合征:最新进展
Indian J Endocrinol Metab. 2011 Sep;15 Suppl 3(Suppl3):S203-7. doi: 10.4103/2230-8210.84869.
5
Sheehan's syndrome with pancytopenia: a case report and review of the literature.席汉综合征伴全血细胞减少症:一例报告并文献复习
J Med Case Rep. 2011 Oct 3;5:490. doi: 10.1186/1752-1947-5-490.
6
Prevalence of hematological abnormalities in patients with Sheehan's syndrome: response to replacement of glucocorticoids and thyroxine.席汉氏综合征患者血液学异常的发生率:糖皮质激素和甲状腺素替代治疗的反应。
Pituitary. 2011 Mar;14(1):39-43. doi: 10.1007/s11102-010-0255-2.
7
Pancytopenia secondary to hypopituitarism may just be due to hypothyroidism alone.垂体功能减退继发的全血细胞减少可能仅由甲状腺功能减退引起。
Ann Hematol. 2010 Nov;89(11):1181. doi: 10.1007/s00277-010-0938-9. Epub 2010 Mar 23.
8
Sheehan's syndrome with pancytopenia--complete recovery after hormone replacement (case series with review).席汉综合征伴全血细胞减少——激素替代治疗后完全康复(病例系列及综述)
Ann Hematol. 2010 Mar;89(3):305-8. doi: 10.1007/s00277-009-0804-9. Epub 2009 Aug 21.
9
[Clinical, laboratory and therapeutics aspects of Sheehan's syndrome].希恩综合征的临床、实验室及治疗方面
Arq Bras Endocrinol Metabol. 2008 Jul;52(5):872-8. doi: 10.1590/s0004-27302008000500020.
10
Sheehan's syndrome.席汉综合征
Pituitary. 2003;6(4):181-8. doi: 10.1023/b:pitu.0000023425.20854.8e.

一例垂体功能减退伴全血细胞减少症经皮质类固醇和甲状腺激素替代治疗治愈。

A case of hypopituitarism with pancytopenia cured by corticosteroid and thyroid hormone replacement therapy.

作者信息

Mladenovic Violeta, Zaric Radica Zivkovic, Sretenovic Snezana, Bubanja Dragana, Ivosevic Zeljko, Igrutinovic Nebojsa, Nesic Jelena, Djurdjevic Predrag

机构信息

Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia.

University Clinical Center Kragujevac, Department of Internal Medicine, Kragujevac, Serbia.

出版信息

Endocrinol Diabetes Metab Case Rep. 2025 Jul 21;2025(3). doi: 10.1530/EDM-24-0119. Print 2025 Jul 1.

DOI:10.1530/EDM-24-0119
PMID:40686398
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12282066/
Abstract

SUMMARY

Pancytopenia associated with hypopituitarism has been reported in the literature as a rare occurrence limited to isolated case reports, predominantly associated with Sheehan syndrome. We present the case of a 31-year-old woman who showed hematological features of pancytopenia and normal cellularity of bone marrow. Hematological investigation disclosed no other cause for pancytopenia. Her physical findings (generalized weakness, slow speech and no pubic or axillary hair) and history of a previous massive postpartum hemorrhage suggested Sheehan's syndrome, and the pituitary hormonal studies revealed panhypopituitarism. Her blood cell accounts were completely recovered after 5 months of glucocorticoid and thyroxine replacement therapy. We hereby report our experience of a cure of pancytopenia and the normal marrow originating from hypopituitarism after corticosteroid and thyroid hormone replacement therapy.

LEARNING POINTS

Sheehan's syndrome correlates with postpartum hemorrhage and causes pancytopenia. It could be successfully treated with glucocorticoid. It could be successfully treated with thyroxine replacement therapy.

摘要

摘要

全血细胞减少症与垂体功能减退相关,在文献中报道为罕见情况,仅限于个别病例报告,主要与席汉综合征有关。我们报告了一名31岁女性的病例,该患者表现出全血细胞减少的血液学特征且骨髓细胞计数正常。血液学检查未发现全血细胞减少的其他原因。她的体格检查结果(全身无力、语速缓慢且无阴毛或腋毛)以及既往大量产后出血史提示席汉综合征,垂体激素检查显示全垂体功能减退。经过5个月的糖皮质激素和甲状腺素替代治疗后,她的血细胞计数完全恢复。我们在此报告糖皮质激素和甲状腺激素替代治疗后治愈垂体功能减退所致全血细胞减少症及正常骨髓的经验。

学习要点

席汉综合征与产后出血相关并导致全血细胞减少症。它可用糖皮质激素成功治疗。它可用甲状腺素替代治疗成功治疗。