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肝和肠系膜纤维肌发育不良:一种罕见病症。

Hepatic and mesenteric fibromuscular dysplasia: an uncommon entity.

作者信息

Ciccarese Zoé, Byl David, Scavee Vincent

机构信息

Department of Vascular surgery, Department of Radiology, Clinique St-Pierre, University affiliated hospital (Université catholique de Louvain), 1340 Ottignies/Louvain-la-Neuve, Belgium.

出版信息

Radiol Case Rep. 2022 Mar 2;17(5):1370-1375. doi: 10.1016/j.radcr.2022.02.009. eCollection 2022 May.

DOI:10.1016/j.radcr.2022.02.009
PMID:35309381
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8927632/
Abstract

Dissection of the common hepatic artery is a rare cause of acute abdomen. In this case report, we discuss a 58-year-old woman who presented with severe epigastric and back pain, for which she had an abdominal computed tomography (CT) scan. On CT images, a dissection of the common hepatic artery, extending to its right and left dividing branches and a diffusely pathological aspect of the hepatic and digestive arterial network was noted. A diagnosis of extensive fibromuscular dysplasia (FMD) was suggested. FMD is a non-atherosclerotic, non-inflammatory arterial disease that most commonly involves the renal and extracranial carotid arteries, but almost all arterial beds may be affected. There is a high prevalence of aneurysm and dissection among patients with FMD.

摘要

肝总动脉夹层是急性腹痛的罕见病因。在本病例报告中,我们讨论一名58岁女性,她因严重的上腹部和背部疼痛就诊,为此进行了腹部计算机断层扫描(CT)。在CT图像上,发现肝总动脉夹层延伸至其左右分支,并且肝和消化动脉网络呈现弥漫性病变。提示诊断为广泛性纤维肌发育不良(FMD)。FMD是一种非动脉粥样硬化、非炎症性动脉疾病,最常累及肾动脉和颅外颈动脉,但几乎所有动脉床都可能受累。FMD患者中动脉瘤和夹层的患病率很高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8626/8927632/ece746dc4e4b/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8626/8927632/bf816badffd5/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8626/8927632/a9d710943ede/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8626/8927632/ece746dc4e4b/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8626/8927632/bf816badffd5/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8626/8927632/a9d710943ede/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8626/8927632/ece746dc4e4b/gr3.jpg

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本文引用的文献

1
Endovascular management of an unsual case of spontaneous Retroperitoneal Haemorrhage due to Fibromuscular Dysplasia.纤维肌性发育异常所致自发性腹膜后出血罕见病例的血管内治疗
CVIR Endovasc. 2020 Sep 9;3:64. doi: 10.1186/s42155-020-00157-8. eCollection 2020 Dec.
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First International Consensus on the diagnosis and management of fibromuscular dysplasia.第一届国际纤维肌发育不良诊断与管理共识会议。
Vasc Med. 2019 Apr;24(2):164-189. doi: 10.1177/1358863X18821816. Epub 2019 Jan 16.
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Fibromuscular Dysplasia: Contemporary Concepts and Future Directions.
纤维肌性发育不良:当代概念与未来方向。
Prog Cardiovasc Dis. 2018 Mar-Apr;60(6):580-585. doi: 10.1016/j.pcad.2018.03.001. Epub 2018 Mar 10.
4
High Prevalence of Multiple Arterial Bed Lesions in Patients With Fibromuscular Dysplasia: The ARCADIA Registry (Assessment of Renal and Cervical Artery Dysplasia).纤维肌发育不良患者的多发性动脉床病变发生率较高:ARCADIA 登记研究(评估肾和颈动脉发育不良)。
Hypertension. 2017 Sep;70(3):652-658. doi: 10.1161/HYPERTENSIONAHA.117.09539. Epub 2017 Jul 17.
5
Fibromuscular dysplasia: Advances in understanding and management.纤维肌性发育异常:认识与管理的进展
Cleve Clin J Med. 2016 Nov;83(11 Suppl 2):S45-S51. doi: 10.3949/ccjm.83.s2.06.
6
Dissection and Aneurysm in Patients With Fibromuscular Dysplasia: Findings From the U.S. Registry for FMD.纤维肌发育不良患者的夹层和动脉瘤:来自美国纤维肌发育不良登记处的研究结果。
J Am Coll Cardiol. 2016 Jul 12;68(2):176-85. doi: 10.1016/j.jacc.2016.04.044.
7
Fibromuscular dysplasia of cervicocephalic arteries: Prevalence of multisite involvement and prognosis.颈脑动脉纤维肌发育不良:多部位受累的患病率及预后
Rev Neurol (Paris). 2015 Sep;171(8-9):616-23. doi: 10.1016/j.neurol.2015.02.011. Epub 2015 Apr 7.
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Recent developments in the understanding and management of fibromuscular dysplasia.纤维肌性发育异常的认识与管理的最新进展
J Am Heart Assoc. 2014 Dec;3(6):e001259. doi: 10.1161/JAHA.114.001259.
9
Fibromuscular dysplasia: state of the science and critical unanswered questions: a scientific statement from the American Heart Association.纤维肌性发育异常:科学现状与关键未解决问题:美国心脏协会的科学声明
Circulation. 2014 Mar 4;129(9):1048-78. doi: 10.1161/01.cir.0000442577.96802.8c. Epub 2014 Feb 18.
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Fibromuscular dysplasia.纤维肌性发育异常
Orphanet J Rare Dis. 2007 Jun 7;2:28. doi: 10.1186/1750-1172-2-28.