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一例导致桡动脉动脉瘤的肌周细胞瘤。

A case of myopericytoma causing radial artery aneurysm.

作者信息

Chehab Mohamad, Kanakaraj Jonathan, Albuquerque Francisco C, Larson Robert A, Levy Mark M, Newton Daniel H

机构信息

Department of Surgery, Virginia Commonwealth University Health System, Richmond, VA.

Department of Pathology, Virginia Commonwealth University Health System, Richmond, VA.

出版信息

J Vasc Surg Cases Innov Tech. 2025 Jun 4;11(5):101869. doi: 10.1016/j.jvscit.2025.101869. eCollection 2025 Oct.

DOI:10.1016/j.jvscit.2025.101869
PMID:40697339
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12281286/
Abstract

A 44-year-old male without history of infection, catheterization, or instrumentation of his left upper extremity presented with a slow-growing pulsatile mass of his forearm. Ultrasound and magnetic resonance imaging revealed a large radial artery aneurysm. Because of worsening paresthesia and pain in his hand, the patient underwent surgical excision of the aneurysm. Pathology revealed an extremely rare case of completely intravascular myopericytoma, originating from the radial artery wall and causing large aneurysmal dilation. Postoperatively, the patient had no vascular or sensorimotor deficits. We suggest that arterial wall myopericytoma can be managed with surgical excision for tissue diagnosis and symptomatic relief.

摘要

一名44岁男性,无左上肢体感染、插管或器械操作史,出现前臂缓慢生长的搏动性肿块。超声和磁共振成像显示为巨大的桡动脉动脉瘤。由于手部感觉异常和疼痛加重,患者接受了动脉瘤手术切除。病理显示为极罕见的完全血管内肌周细胞瘤,起源于桡动脉壁并导致巨大动脉瘤样扩张。术后,患者无血管或感觉运动功能障碍。我们建议,动脉壁肌周细胞瘤可通过手术切除进行组织诊断并缓解症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fbe/12281286/da4860d6804b/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fbe/12281286/7e2c7ffcfdd0/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fbe/12281286/15ac2cc5738a/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fbe/12281286/dc5ab652f128/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fbe/12281286/da4860d6804b/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fbe/12281286/7e2c7ffcfdd0/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fbe/12281286/15ac2cc5738a/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fbe/12281286/dc5ab652f128/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fbe/12281286/da4860d6804b/gr4.jpg

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本文引用的文献

1
Spontaneous deep vein thrombosis of the upper arm due to an intravascular myopericytoma: A case report and literature review.因血管肌纤维母细胞瘤导致的上臂自发性深静脉血栓形成:病例报告及文献复习。
Medicine (Baltimore). 2023 Dec 8;102(49):e36566. doi: 10.1097/MD.0000000000036566.
2
Rare Case of Intravascular Myopericytoma-Imaging Characteristics and Review of the Literature.血管内肌周细胞瘤罕见病例——影像学特征及文献综述
Diagnostics (Basel). 2022 Oct 13;12(10):2473. doi: 10.3390/diagnostics12102473.
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Malignant myopericytoma: Case report and review of the literature.
恶性肌纤维母细胞瘤:病例报告及文献复习。
J Cutan Pathol. 2023 Jan;50(1):39-42. doi: 10.1111/cup.14313. Epub 2022 Sep 12.
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Myopericytoma: A Review of Twenty-Three Cases Over Twelve Years and a Case Report of a Rare Neoplasm.肌纤维母细胞肉瘤:十二年 23 例回顾及一种罕见肿瘤的病例报告。
Am J Dermatopathol. 2022 Sep 1;44(9):623-631. doi: 10.1097/DAD.0000000000002130. Epub 2022 Apr 27.
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Intravascular myopericytoma on the right dorsal foot.右足背内侧血管内肌周细胞瘤
Eur J Dermatol. 2020 Dec 1;30(6):736-737. doi: 10.1684/ejd.2020.3906.
6
Primary malignant myopericytoma with cancer cachexia: Report of the first case and review of literature.伴有癌性恶病质的原发性恶性肌周细胞瘤:首例病例报告及文献复习
Medicine (Baltimore). 2017 Dec;96(49):e9064. doi: 10.1097/MD.0000000000009064.
7
Malignant Myopericytoma of Shoulder: A Rare Lesion.肩部恶性肌周细胞瘤:一种罕见病变
APSP J Case Rep. 2016 Jun 15;7(3):21. doi: 10.21699/ajcr.v7i3.421. eCollection 2016 Jul-Aug.
8
Malignant Myopericytoma: Report of a New Case and Review of the Literature.恶性肌周细胞瘤:一例新病例报告及文献复习
Am J Dermatopathol. 2016 Apr;38(4):307-11. doi: 10.1097/DAD.0000000000000463.
9
Digital artery intravascular myopericytoma--a rare cause of a painful finger.指动脉血管内肌周细胞瘤——手指疼痛的罕见病因。
J Hand Surg Eur Vol. 2015 Sep;40(7):753-4. doi: 10.1177/1753193414534380. Epub 2014 May 6.
10
Intravascular myopericytoma beside the shinbone: a rare histological variant.胫骨旁血管内肌周细胞瘤:一种罕见的组织学变异型
J Clin Pathol. 2009 Sep;62(9):862-3. doi: 10.1136/jcp.2009.065672.