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BMJ Case Rep. 2021 May 31;14(5):e240105. doi: 10.1136/bcr-2020-240105.
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Pituitary Apoplexy in Patients with Pituitary Neuroendocrine Tumors (PitNET).垂体神经内分泌肿瘤(PitNET)患者的垂体卒中
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本文引用的文献

1
SOCIETY FOR ENDOCRINOLOGY ENDOCRINE EMERGENCY GUIDANCE: Emergency management of pituitary apoplexy in adult patients.内分泌学会内分泌急症指南:成年患者垂体卒中的应急管理
Endocr Connect. 2016 Sep;5(5):G12-G15. doi: 10.1530/EC-16-0057.
2
[Primary immune thrombocytopenia accompanied by pituitary apoplexy].原发性免疫性血小板减少症伴垂体卒中
Rinsho Ketsueki. 2016 Jul;57(7):877-80. doi: 10.11406/rinketsu.57.877.
3
Bleeding complications in immune thrombocytopenia.免疫性血小板减少症的出血并发症
Hematology Am Soc Hematol Educ Program. 2015;2015:237-42. doi: 10.1182/asheducation-2015.1.237.
4
Pituitary Apoplexy.垂体卒中。
Endocr Rev. 2015 Dec;36(6):622-45. doi: 10.1210/er.2015-1042. Epub 2015 Sep 28.
5
The incidence of idiopathic thrombocytopenic purpura among adults: a population-based study and literature review.成人特发性血小板减少性紫癜的发病率:一项基于人群的研究及文献综述
Eur J Haematol. 2009 Aug;83(2):83-9. doi: 10.1111/j.1600-0609.2009.01247.x. Epub 2009 Feb 23.
6
Pituitary apoplexy and idiopathic thrombocytopenic purpura: a new case and review of the literature.垂体卒中与特发性血小板减少性紫癜:1例新病例及文献复习
Pituitary. 2004;7(3):189-192. doi: 10.1007/s11102-005-1760-6.
7
Guidelines for the investigation and management of idiopathic thrombocytopenic purpura in adults, children and in pregnancy.成人、儿童及妊娠期特发性血小板减少性紫癜的调查与管理指南
Br J Haematol. 2003 Feb;120(4):574-96. doi: 10.1046/j.1365-2141.2003.04131.x.
8
Pituitary apoplexy with optic tract oedema and haemorrhage in a patient with idiopathic thrombocytopenic purpura.一名特发性血小板减少性紫癜患者发生垂体卒中伴视束水肿和出血。
Neuroradiology. 2001 Feb;43(2):156-8. doi: 10.1007/s002340000390.
9
Pituitary apoplexy: its incidence and clinical significance.垂体卒中:其发病率及临床意义。
J Neurosurg. 1981 Aug;55(2):187-93. doi: 10.3171/jns.1981.55.2.0187.
10
Hemorrhage, necrosis, and apoplexy in pituitary adenomas.垂体腺瘤中的出血、坏死和卒中。
Surg Neurol. 1982 Sep;18(3):181-9. doi: 10.1016/0090-3019(82)90388-3.

已知垂体大腺瘤患者因免疫性血小板减少症引起的出血导致垂体卒中及相关颅神经麻痹。

Pituitary apoplexy and associated cranial nerve palsies secondary to bleeding caused by immune thrombocytopaenia in a patient with known pituitary macroadenoma.

机构信息

Department of Medicine for the Elderly, Luton and Dunstable University Hospital NHS Foundation Trust, Luton, UK

Department of Medicine for the Elderly, Luton and Dunstable University Hospital NHS Foundation Trust, Luton, UK.

出版信息

BMJ Case Rep. 2021 May 31;14(5):e240105. doi: 10.1136/bcr-2020-240105.

DOI:10.1136/bcr-2020-240105
PMID:34059534
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8169482/
Abstract

An 84-year-old man presented with a frontal headache and easy bruising. He had a background history of a pituitary macroadenoma, diagnosed incidentally a year earlier. Investigations showed haemorrhage into the pituitary macroadenoma leading to a diagnosis of pituitary apoplexy in the context of low platelet count secondary to immune thrombocytopaenia. He was treated with intravenous hydrocortisone, platelet transfusion, intravenous immunoglobulin and high-dose steroid. Neurosurgical intervention was not indicated initially. Five days into his admission, he developed bilateral ptosis and ophthalmoplegia. MRI confirmed further haemorrhage associated with compression of the optic chiasm. He was transferred to a tertiary neurosurgical centre where he underwent urgent surgical decompression. To date, there has been minor improvement in his neurological symptoms. Management of this patient required considerable multidisciplinary teamwork between the clinics of endocrinology, haematology, neurosurgery, ophthalmology and geriatrics.

摘要

一位 84 岁男性因额部头痛和容易瘀伤就诊。他有垂体大腺瘤的既往病史,一年前偶然诊断出。检查显示垂体大腺瘤内出血,导致低血小板计数继发免疫性血小板减少症的垂体卒中诊断。他接受了静脉注射氢化可的松、血小板输注、静脉注射免疫球蛋白和大剂量类固醇治疗。最初不建议神经外科干预。入院 5 天后,他出现双侧上睑下垂和眼肌麻痹。MRI 证实与视交叉受压相关的进一步出血。他被转至三级神经外科中心,接受紧急手术减压。迄今为止,他的神经症状有轻微改善。对该患者的治疗需要内分泌科、血液科、神经外科、眼科和老年科之间的多学科团队进行大量协作。