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

Q3 Medicine
European journal of case reports in internal medicine Pub Date : 2024-12-16 eCollection Date: 2024-01-01 DOI:10.12890/2024_005056
Mahmoud Farouk Kamel Hassanein, Alaa Ebrahim, Stephanie Alcine Joseph, Teresa Jack, Ramprasath Anbazhagan, Miguel Fernández Olivares, Olena Kovalska
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引用次数: 0

Abstract

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.

活动性狼疮患者上臂深静脉血栓形成。
上肢深静脉血栓形成(UEDVT)相对罕见,更少作为系统性红斑狼疮(SLE)的初始表现。原发性UEDVT应考虑在个体单侧手臂肿胀,臂静脉,腋窝静脉,锁骨下静脉经常受累。SLE是一种慢性自身免疫性疾病,主要影响育龄妇女和非洲人后裔。患者的临床特征从关节炎和关节痛(超过90%的SLE患者)到危及生命的血液病或中枢神经系统受累。个体动脉和/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,血栓性事件通常见于腿部,UEDVT仍然是一种不寻常的表现。在这里,我们提出一个36岁的非洲裔女性的病例,最近的病史是小关节关节痛和阴道出血,由于子宫肌瘤,她开了一个短期疗程的泼尼松龙和去甲睾酮。她有两周的左臂单侧肿胀史。多普勒超声和后来的计算机断层扫描显示左侧UEDVT。入院期间的进一步检查最终诊断为SLE,而抗磷脂综合征——SLE中常见的血栓形成因素——被明显排除。病人开始使用抗凝剂。病人后来迅速发展为狼疮肾炎,并开始服用大剂量强的松龙。考虑到出血的高风险,我们决定推迟肾活检。与下肢深静脉血栓形成相比,UEDVT的可用数据有限,无抗磷脂综合征的SLE患者血栓形成的研究更少。记住这一点,临床医生需要认识到特发性UEDVT是SLE的潜在早期征兆,并保持高度怀疑。学习要点:强调自发性单侧手臂肿胀中特发性上肢深静脉血栓形成(UEDVT)的可能性。在这种情况下,特发性UEDVT可能表明严重的潜在自身免疫性疾病,如SLE(没有抗磷脂综合征),这需要多学科团队的深入调查。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适当的初始治疗,而肾脏活检可能没有必要,因为抗凝剂的出血风险很高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
166
审稿时长
8 weeks
期刊介绍: The European Journal of Case Reports in Internal Medicine is an official journal of the European Federation of Internal Medicine (EFIM), representing 35 national societies from 33 European countries. The Journal''s mission is to promote the best medical practice and innovation in the field of acute and general medicine. It also provides a forum for internal medicine doctors where they can share new approaches with the aim of improving diagnostic and clinical skills in this field. EJCRIM welcomes high-quality case reports describing unusual or complex cases that an internist may encounter in everyday practice. The cases should either demonstrate the appropriateness of a diagnostic/therapeutic approach, describe a new procedure or maneuver, or show unusual manifestations of a disease or unexpected reactions. The Journal only accepts and publishes those case reports whose learning points provide new insight and/or contribute to advancing medical knowledge both in terms of diagnostics and therapeutic approaches. Case reports of medical errors, therefore, are also welcome as long as they provide innovative measures on how to prevent them in the current practice (Instructive Errors). The Journal may also consider brief and reasoned reports on issues relevant to the practice of Internal Medicine, as well as Abstracts submitted to the scientific meetings of acknowledged medical societies.
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