Ritter Einat, Itach Tamar, Paran Daphna, Gaskin Aleksandr, Havakuk Ofer, Ablin Jacob Nadav
Department of Gastroenterology and Liver Diseases, Tel Aviv Sourasky Medical Center, Tel Aviv 64239, Israel.
Department of Cardiology, Tel Aviv Sourasky Medical Center, Tel Aviv 64239, Israel.
J Clin Med. 2024 Jul 25;13(15):4345. doi: 10.3390/jcm13154345.
We present the case of a 39-year-old woman who was diagnosed with SLE and antiphospholipid antibodies 8 years ago. The chief manifestations of her disease included low-grade fever and polyarthritis. Eight months before presentation, she experienced symptoms attributed to a flare of SLE, leading to an increase in immunomodulatory treatment with no improvement. She presented to the emergency room with acute onset of dyspnea. Clubbing of her fingers and toes was noted. When questioned, she reported the onset of clubbing 5 months earlier. A CTA was performed to rule out pulmonary embolism, which was excluded, although it revealed a severely damaged mitral valve with severe insufficiency and a large mass on the valve, protruding into the left atrium. Antibiotics were started, with a working diagnosis of infectious endocarditis; however, the severe mitral valve dysfunction lead to emergency mitral valve replacement, revealing an organized thrombus. She was treated with anticoagulation, with a working diagnosis of Libman-Sacks endocarditis, with no improvement. Additional immunosuppression failed to improve her symptoms. Enlargement of the thrombotic mass and an increased gradient across the prosthetic mitral valve led to repeat surgery, culminating in a diagnosis of high-grade sarcoma within the left atrial mass. We further discuss cardiac sarcoma and describe the occurrence of clubbing in patients with sarcoma. This case highlights the importance of interdisciplinary collaboration and the need for vigilant monitoring in refractory cases, particularly when atypical presentations arise.
我们报告了一例39岁女性病例,该患者8年前被诊断为系统性红斑狼疮(SLE)并伴有抗磷脂抗体。其疾病的主要表现包括低热和多关节炎。就诊前8个月,她出现了归因于SLE病情活动的症状,导致免疫调节治疗增加但无改善。她因急性呼吸困难就诊于急诊室。发现其手指和脚趾杵状指。询问时,她报告杵状指在5个月前开始出现。进行了CT血管造影(CTA)以排除肺栓塞,尽管排除了肺栓塞,但显示二尖瓣严重受损,伴有严重关闭不全,且瓣膜上有一个大肿块,突入左心房。开始使用抗生素,初步诊断为感染性心内膜炎;然而,严重的二尖瓣功能障碍导致紧急二尖瓣置换,结果发现是一个机化血栓。她接受了抗凝治疗,初步诊断为Libman-Sacks心内膜炎,但症状无改善。额外的免疫抑制治疗也未能改善她的症状。血栓性肿块增大以及人工二尖瓣跨瓣压差增加导致再次手术,最终诊断左心房肿块为高级别肉瘤。我们进一步讨论心脏肉瘤,并描述肉瘤患者中杵状指的发生情况。该病例强调了跨学科协作的重要性以及在难治性病例中进行密切监测的必要性,特别是当出现非典型表现时。