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一名活动性狼疮患者的上臂深静脉血栓形成

Upper Arm Deep Vein Thrombosis in a Patient with Active Lupus.

作者信息

Hassanein Mahmoud Farouk Kamel, Ebrahim Alaa, Joseph Stephanie Alcine, Jack Teresa, Anbazhagan Ramprasath, Olivares Miguel Fernández, Kovalska Olena

机构信息

Department of Internal Medicine, Seychelles Hospital, Healthcare Agency, Victoria, Seychelles.

Nephrology Division, Seychelles Hospital, Healthcare Agency, Victoria, Seychelles.

出版信息

Eur J Case Rep Intern Med. 2024 Dec 16;11(12):005056. doi: 10.12890/2024_005056. eCollection 2024.

Abstract

UNLABELLED

Upper extremity deep vein thrombosis (UEDVT) is relatively rare, and much less as an initial presentation of systemic lupus erythematosus (SLE). Primary UEDVT should be considered in individuals with unilateral arm swelling where the brachial, axillary, and subclavian veins are frequently involved. SLE is a chronic autoimmune disease that predominantly affects women of childbearing age and of African descent. Patients present with clinical features ranging from arthritis and arthralgias (over 90% of patients with SLE) to life-threatening hematologic, or central nervous system involvement. Individuals have an increased risk of arterial and/or venous thrombosis where the most important risk factor is the presence of antiphospholipid antibodies. Even within this condition, thrombotic events are typically seen in the legs, and UEDVT remains an unusual presentation. Here, we present a case of a 36-year-old female of African descent with a recent medical history of small joint arthralgia and vaginal bleeding due to uterine fibroids, for which she was prescribed a short course of prednisolone and norethisterone, respectively. She presented with a 2-week history of unilateral swelling in the left arm. Doppler ultrasound and later computed tomography scan with contrast indicated left UEDVT. Further investigations throughout her admission led to the diagnosis of SLE, while antiphospholipid syndrome - a common contributor to thrombosis in SLE - was notably ruled out. The patient was initiated on anticoagulants. The patient went on to later rapidly develop lupus nephritis and started on high-dose prednisolone. Given the high risk of bleeding, the decision to postpone the kidney biopsy was taken. There is limited data available about UEDVT when compared to lower extremity DVT and even fewer studies on SLE patients with thrombosis in the absence of antiphospholipid syndrome. Keeping this in mind, clinicians need to recognize idiopathic UEDVT as a potential early sign of SLE and maintain a high level of suspicion.

LEARNING POINTS

To highlight the possibility of idiopathic upper extremity deep vein thrombosis (UEDVT) in spontaneous unilateral arm swelling.Idiopathic UEDVT might indicate a serious underlying autoimmune condition as SLE in this case (in the absence of antiphospholipid syndrome), that requires intensive thorough investigation by a multidisciplinary team.Initial treatment of both UEDVT and lupus nephritis with standard dose anticoagulants and steroids might be the proper initial management, whereas kidney biopsy might not be necessary as the risk of bleeding is high while on anticoagulants.

摘要

未标注

上肢深静脉血栓形成(UEDVT)相对罕见,作为系统性红斑狼疮(SLE)的初始表现则更为少见。对于出现单侧手臂肿胀且肱静脉、腋静脉和锁骨下静脉常受累的个体,应考虑原发性UEDVT。SLE是一种慢性自身免疫性疾病,主要影响育龄期女性和非洲裔女性。患者的临床特征范围广泛,从关节炎和关节痛(超过90%的SLE患者)到危及生命的血液系统或中枢神经系统受累。个体发生动脉和/或静脉血栓形成的风险增加,其中最重要的危险因素是抗磷脂抗体的存在。即使在这种情况下,血栓形成事件通常见于腿部,UEDVT仍然是一种不常见的表现。在此,我们报告一例36岁非洲裔女性病例,她近期有小关节关节痛病史,因子宫肌瘤出现阴道出血,为此分别接受了短期泼尼松龙和炔诺酮治疗。她出现了左臂单侧肿胀2周的病史。多普勒超声及后来的增强计算机断层扫描显示左侧UEDVT。她入院后的进一步检查导致诊断为SLE,而抗磷脂综合征(SLE中血栓形成的常见原因)被明确排除。患者开始接受抗凝治疗。该患者后来迅速发展为狼疮性肾炎,并开始使用大剂量泼尼松龙治疗。鉴于出血风险高,决定推迟肾活检。与下肢深静脉血栓形成相比,关于UEDVT的数据有限,而关于无抗磷脂综合征的SLE血栓形成患者的研究更少。考虑到这一点,临床医生需要认识到特发性UEDVT可能是SLE的潜在早期迹象,并保持高度怀疑。

学习要点

强调自发性单侧手臂肿胀时特发性上肢深静脉血栓形成(UEDVT)的可能性。在这种情况下(无抗磷脂综合征),特发性UEDVT可能提示一种严重的潜在自身免疫性疾病,如SLE,这需要多学科团队进行深入全面的调查。UEDVT和狼疮性肾炎的初始治疗采用标准剂量的抗凝剂和类固醇可能是合适的初始管理方法,而在使用抗凝剂时,由于出血风险高,肾活检可能没有必要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9f4/11716306/d347b8adfd90/5056_Fig1.jpg

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