Diaz-Navarro Rienzi A, Kerkhof Peter L M
Dept. Internal Medicine, School of Medicine and Center for Biomedical Research, Universidad de Valparaiso, Viña del Mar 2540064, Chile.
Dept. Radiology & Nuclear Medicine, Amsterdam University Medical Centers, location VUmc, Amsterdam 1007 MB, The Netherlands.
Eur Heart J Case Rep. 2022 Sep 15;6(9):ytac376. doi: 10.1093/ehjcr/ytac376. eCollection 2022 Sep.
Right ventricular mural endocarditis (RVME) is an extremely rare type of infective endocarditis that can occur even in the absence of predisposing factors. The diagnosis is a challenge when no causative pathogen can be detected.
A previously healthy young man was admitted to a local hospital with a diagnosis of prolonged febrile syndrome and treated for acute sinusitis. As complaints returned, he was hospitalized 3 weeks later, where an echocardiogram demonstrated multiple mobile masses in the right ventricle, and a computed tomography scan revealed extensive pulmonary thromboembolism. During surgery, the endocardial masses were excised, and the pathologist considered an inflammatory myofibroblastic tumour. Despite appropriate medication and initial improvements, the complaints persisted, and 2 weeks after the surgery, the patient returned to the hospital. Imaging studies documented reappearance to the previous findings, whereas blood cultures remained negative. During the second surgery, the new masses resembling vegetations were excised, and histologic analysis indicated infective endocarditis. Adjusted medication was given for 30 days. Just before discharge, no vegetations were seen. At follow-up, 5 years later, he was in a healthy condition.
Despite careful examinations, initial treatments according to standard protocols were unsuccessful. At final discharge, the patient reported that a tattoo complication prior to the first hospitalization was treated by antibiotics but that he did not complete the course. This omission in the communication further complicated the diagnostic and management processes, leading to surgical interventions that could have been prevented if the neglected antibiotic course was properly disclosed.
右心室壁性心内膜炎(RVME)是一种极其罕见的感染性心内膜炎类型,即使在没有易感因素的情况下也可能发生。当无法检测到致病病原体时,诊断具有挑战性。
一名既往健康的年轻男性因长期发热综合征入院,最初诊断为急性鼻窦炎并接受治疗。由于症状复发,3周后他再次住院,超声心动图显示右心室有多个活动团块,计算机断层扫描显示广泛的肺血栓栓塞。手术中切除了心内膜团块,病理学家考虑为炎性肌纤维母细胞瘤。尽管给予了适当的药物治疗且病情初步改善,但症状仍持续存在,术后2周患者再次入院。影像学检查记录到先前的病变再次出现,而血培养仍为阴性。第二次手术切除了类似赘生物的新团块,组织学分析表明为感染性心内膜炎。调整用药30天。出院前未见赘生物。5年后随访时,他身体健康。
尽管进行了仔细检查,但按照标准方案进行的初始治疗未成功。在最终出院时,患者报告首次住院前纹身出现并发症曾接受抗生素治疗,但未完成疗程。沟通中的这一疏漏使诊断和管理过程更加复杂,如果能正确披露被忽视的抗生素疗程,本可避免手术干预。