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Clin Case Rep. 2023 Jan 23;11(1):e6827. doi: 10.1002/ccr3.6827. eCollection 2023 Jan.
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Sheehan's syndrome: new insights into an old disease.希恩综合征:对一种古老疾病的新见解。
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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.
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Recurrent symptomatic hypoglycaemia with pancytopenia as a delayed presentation of Sheehan's syndrome with complete recovery after hormone replacement.复发性症状性低血糖伴全血细胞减少,为席汉综合征的延迟表现,激素替代治疗后完全康复。
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本文引用的文献

1
A case report of Sheehan's syndrome with acute onset, hyponatremia and severe anemia.希恩综合征伴急性起病、低钠血症和严重贫血的病例报告。
Acta Biomed. 2009 Apr;80(1):73-6.
2
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.
3
Sheehan's syndrome as a rare cause of anaemia secondary to hypopituitarism.席汉综合征是垂体功能减退继发贫血的罕见病因。
Ann Hematol. 2009 May;88(5):405-10. doi: 10.1007/s00277-008-0607-4. Epub 2008 Sep 17.
4
An unusual case of pancytopenia associated with Sheehan's syndrome.一例与席汉综合征相关的全血细胞减少症罕见病例。
Ann Hematol. 2007 Apr;86(4):307-8. doi: 10.1007/s00277-006-0233-y. Epub 2007 Jan 4.
5
Sheehan's syndrome associated with pancytopenia due to marrow aplasia; full recovery with hormone replacement therapy.希恩综合征伴骨髓再生障碍所致全血细胞减少;激素替代疗法后完全康复。
Int J Clin Pract. 2004 May;58(5):533-5. doi: 10.1111/j.1368-5031.2004.00059.x.
6
Case of complete recovery of pancytopenia after treatment of hypopituitarism.垂体功能减退症治疗后全血细胞减少完全恢复的病例。
Ann Hematol. 2004 May;83(5):309-12. doi: 10.1007/s00277-003-0800-4. Epub 2003 Nov 26.
7
Demonstration of reserved anterior pituitary function among patients with amenorrhea after postpartum hemorrhage.产后出血后闭经患者垂体前叶储备功能的表现
Gynecol Endocrinol. 2000 Apr;14(2):99-104. doi: 10.3109/09513590009167667.
8
Sheehan's syndrome with complete bone marrow aplasia: long-term results of substitution therapy with hormones.席汉综合征伴全骨髓再生障碍:激素替代治疗的长期结果
Br J Haematol. 1976 Aug;33(4):575-82. doi: 10.1111/j.1365-2141.1976.tb03576.x.

席汉综合征伴全血细胞减少症:一例报告并文献复习

Sheehan's syndrome with pancytopenia: a case report and review of the literature.

作者信息

Fatma Mnif, Mouna Elleuch, Nabila Rekik, Mouna Mnif, Nadia Charfi, Mohamed Abid

机构信息

Endocrinology Department, Hedi Chaker Hospital, (3029) Sfax, Tunisia.

出版信息

J Med Case Rep. 2011 Oct 3;5:490. doi: 10.1186/1752-1947-5-490.

DOI:10.1186/1752-1947-5-490
PMID:21968051
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3197536/
Abstract

INTRODUCTION

Sheehan's syndrome is defined by varying degrees of anterior pituitary deficiency due to postpartum ischemic necrosis of the pituitary gland after massive bleeding. It is a rare disorder in western countries and even in Tunisia. Hematologic abnormalities such as normochromic anemia have been reported in these patients. However, pancytopenia is rarely observed.

CASE PRESENTATION

We describe the case of a 48-year-old Tunisian woman with features of hypopituitarism. Laboratory tests showed pancytopenia that was completely reversed after adequate hormone replacement.

CONCLUSION

Clinicians should consider the possibility of hypopituitarism as a cause of pancytopenia. This is an original case report that is of interest to hematologists, who should be aware of Sheehan's syndrome as a treatable etiology of pancytopenia for women.

摘要

引言

席汉综合征是指产后垂体大量出血后发生缺血性坏死,导致不同程度的垂体前叶功能减退。在西方国家甚至突尼斯,这都是一种罕见的疾病。这些患者曾有正色素性贫血等血液学异常情况报道。然而,全血细胞减少很少见。

病例报告

我们描述了一名48岁突尼斯女性垂体功能减退的病例。实验室检查显示全血细胞减少,在进行充分的激素替代治疗后完全逆转。

结论

临床医生应考虑垂体功能减退作为全血细胞减少病因的可能性。这是一份原创病例报告,血液科医生应予以关注,他们应意识到席汉综合征是女性全血细胞减少的一种可治疗病因。