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一例由甲氨蝶呤相关淋巴增殖性疾病引起的股动脉瘤病例。

A Case of Femoral Artery Aneurysm Caused by Methotrexate Associated Lymphoproliferative Disease.

作者信息

Harada Atsushi, Nishihara Masahiro, Takahashi Hiromichi, Machii Yojiro, Tanaka Masashi

机构信息

Department of Cardiovascular Surgery, Nihon University School of Medicine, Tokyo, JPN.

Department of Rheumatology and Collagen Medicine, Nihon University School of Medicine, Tokyo, JPN.

出版信息

Cureus. 2024 Apr 9;16(4):e57933. doi: 10.7759/cureus.57933. eCollection 2024 Apr.

Abstract

An 82-year-old man with left leg edema was referred to our department after an ultrasound examination by his previous physician, which revealed deep vein thrombosis (DVT) in the left superficial femoral vein and a left common femoral artery aneurysm (CFAA). The DVT was caused by the CFAA. The patient was adjudged to be at high risk of peripheral embolization due to the irregular shape of the varicose vein and a large amount of mural thrombus. Surgery was performed to replace the artificial blood vessel. The patient displayed firm adhesion to the surrounding area, marked lymph node swelling, and a large amount of mural thrombus in the mass. The superficial femoral artery (SFA) demonstrated severe intimal thickening and partial dissection. The postoperative course was good, and the patient was undergoing rehabilitation to be discharged home; however, B-cell lymphoma was suspected based on the pathology results of the mass wall submitted intraoperatively. The patient had a history of rheumatoid arthritis and was treated with methotrexate (MTX). During the course of his illness, a subcutaneous mass was found on his right forearm, and a skin biopsy revealed MTX-associated lymphoproliferative disease (MTX-LPD), which had resolved with MTX withdrawal. The histopathological results of the skin biopsy matched those of the CFAA mural thrombus, and Epstein-Barr virus-positive cells were also observed, leading to the diagnosis of MTX-LPD, which was considered to be the cause of CFAA. No MTX-LPD was identified in the vessel walls or intramural thrombus. We herein report a case of CFAA with an extremely rare etiology and clinical presentation.

摘要

一名82岁左腿水肿男性患者经前一位医生超声检查后转诊至我科,检查发现左股浅静脉深静脉血栓形成(DVT)及左股总动脉瘤(CFAA)。DVT由CFAA引起。由于静脉曲张形状不规则及大量壁血栓,该患者被判定有外周栓塞的高风险。遂行手术置换人工血管。患者肿物与周围区域粘连紧密,淋巴结明显肿大,肿物内有大量壁血栓。股浅动脉(SFA)显示严重内膜增厚及部分夹层。术后病程顺利,患者正在接受康复治疗准备出院;然而,根据术中送检肿物壁的病理结果怀疑为B细胞淋巴瘤。患者有类风湿关节炎病史,曾用甲氨蝶呤(MTX)治疗。病程中,其右前臂发现一个皮下肿物,皮肤活检显示为MTX相关淋巴增殖性疾病(MTX-LPD),停用MTX后已缓解。皮肤活检的组织病理学结果与CFAA壁血栓的结果相符,且还观察到爱泼斯坦-巴尔病毒阳性细胞,从而诊断为MTX-LPD,认为其为CFAA的病因。在血管壁或壁内血栓中未发现MTX-LPD。我们在此报告一例病因及临床表现极为罕见的CFAA病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e7e/11082078/327b784d0b18/cureus-0016-00000057933-i01.jpg

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