Li Xiaohui, Lu Rugang, Zhao Youcai, Wang Feng, Shao Guoqiang
Department of Radiology, Nanjing Children's Hospital Affiliated to Nanjing Medical University, Nanjing 210008, P.R. China.
Department of Urinary Surgery, Nanjing Children's Hospital Affiliated to Nanjing Medical University, Nanjing 210008, P.R. China.
Mol Clin Oncol. 2018 Jun;8(6):725-728. doi: 10.3892/mco.2018.1604. Epub 2018 Apr 12.
Primary malignant pericardial mesothelioma (PMPM) is an aggressive tumor that originates from the mesothelial cells of the pericardium. PMPM with extensive atrial infiltration and bone metastasis is extremely rare. The diagnosis and staging of PMPM based on anatomical imaging may be difficult when concurrent pericardial and pleural effusions are present. A 28-year-old man presented with progressive chest pain. Concurrent pericardial and pleural effusions were identified on computed tomography. On echocardiography, mild thickening and adhesions of the pericardium with the right ventricle and atrium were observed. F-fluorodeoxyglucose (FDG) metabolism imaging revealed increased accumulation in the pericardium and adjacent right atrium. Ring-shaped radioactivity aggregation and bone destruction in the sacrum were demonstrated on F-FDG and Tc-methyl diphosphonate imaging. The diagnosis of PMPM was subsequently confirmed by pathology. The patient survived for >1.5 years with comprehensive treatment.
原发性恶性心包间皮瘤(PMPM)是一种起源于心包间皮细胞的侵袭性肿瘤。伴有广泛心房浸润和骨转移的PMPM极为罕见。当同时存在心包和胸腔积液时,基于解剖学成像对PMPM进行诊断和分期可能会很困难。一名28岁男性出现进行性胸痛。计算机断层扫描发现同时存在心包和胸腔积液。超声心动图显示心包与右心室和心房轻度增厚并粘连。F-氟脱氧葡萄糖(FDG)代谢成像显示心包和相邻右心房摄取增加。F-FDG和锝-亚甲基二膦酸盐成像显示骶骨有环形放射性聚集和骨质破坏。随后经病理证实为PMPM。该患者经综合治疗存活超过1.5年。