Sood Akhil, Chiadika Simbo M, Everett Jamie M, Au Jason, Rowe Julie
Internal Medicine, University of Texas Health Science Center at Houston-Mcgovern Medical School, Houston, USA.
Internal Medicine, Division of Cardiovascular Medicine, University of Texas Health Science Center at Houston-Mcgovern Medical School, Houston, USA.
Cureus. 2018 Sep 6;10(9):e3261. doi: 10.7759/cureus.3261.
Neuroendocrine tumors (NETs) are rare malignant tumors that arise from neuroendocrine cells of the gastrointestinal tract and often metastasize to the liver, lung, and bone. Cardiac metastasis of NETs is uncommon. We report a patient with a past medical history of a neuroendocrine tumor of the left femur presenting with signs and symptoms of new onset heart failure. Transthoracic echocardiogram and cardiac magnetic resonance showed a large mass within the right ventricle causing right ventricular outflow obstruction. A positron emission tomographic/computed tomographic scan (PET-CT) revealed increased uptake of fluorodeoxyglucose (FDG) activity within the right ventricle consistent with metastasis. Cardiac biopsy of the right ventricular mass revealed metastatic nonfunctioning neuroendocrine tumor. In view of the fact that it was a tumor that caused the right ventricular obstruction, the patient was started on chemotherapy with improvement of symptoms. This case highlights that in patients with a history of neuroendocrine tumor presenting with heart failure, cardiac metastasis should be included in the differential.
神经内分泌肿瘤(NETs)是起源于胃肠道神经内分泌细胞的罕见恶性肿瘤,常转移至肝脏、肺和骨骼。NETs的心脏转移并不常见。我们报告一例既往有左股骨神经内分泌肿瘤病史的患者,出现新发心力衰竭的体征和症状。经胸超声心动图和心脏磁共振显示右心室内有一个大肿块,导致右心室流出道梗阻。正电子发射断层扫描/计算机断层扫描(PET-CT)显示右心室内氟脱氧葡萄糖(FDG)活性摄取增加,符合转移表现。右心室肿块的心脏活检显示为转移性无功能神经内分泌肿瘤。鉴于该肿瘤导致了右心室梗阻,患者开始接受化疗,症状有所改善。该病例强调,对于有神经内分泌肿瘤病史且出现心力衰竭的患者,鉴别诊断时应考虑心脏转移。