Eto Ryo, Kawano Hiroaki, Horie Ichiro, Kaneko Kenichi, Honda Takuya, Abe Kuniko, Koga Seiji, Ikeda Satoshi, Maemura Koji
Department of Cardiovascular Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Department of Endocrinology and Metabolism, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
J Cardiol Cases. 2019 Oct 20;21(2):63-66. doi: 10.1016/j.jccase.2019.10.001. eCollection 2020 Feb.
A 65-year-old Japanese woman with an intrapericardial tumor and neck tumor was admitted to our hospital. Intrapericardial tumor had not been resected because of massive bleeding from the hypervascular tumor and its invasion into the pericardium, ascending aorta, and pulmonary artery. The neck tumor had been successfully resected, and paraganglioma was pathologically diagnosed. Abnormal accumulation in the intrapericardial tumor was seen with I-metaiodobenzylguanidine scintigraphy. Moreover, gene mutation of succinate dehydrogenase type D was found. Finally, paraganglioma of the carotid body and intrapericardium was diagnosed. < Cardiac paraganglioma (PGL) and simultaneous carotid body and cardiac PGL is exceedingly rare. We experienced a case of intrapericardial tumor and carotid body tumor, evaluated by histological examination of the surgical specimen of the carotid body tumor and multimodal imaging including I-metaiodobenzylguanidine scintigraphy, and genetic analysis of the succinate dehydrogenase gene. The final diagnosis was type 1 PGLs of both the carotid body and intrapericardium.>.
一名患有心包内肿瘤和颈部肿瘤的65岁日本女性入住我院。由于高血管性肿瘤大量出血及其侵犯心包、升主动脉和肺动脉,心包内肿瘤未行切除。颈部肿瘤已成功切除,病理诊断为副神经节瘤。间碘苄胍闪烁显像显示心包内肿瘤有异常聚集。此外,发现了D型琥珀酸脱氢酶基因突变。最终诊断为颈动脉体和心包副神经节瘤。<心脏副神经节瘤(PGL)以及同时发生的颈动脉体和心脏PGL极其罕见。我们遇到了一例心包内肿瘤和颈动脉体肿瘤的病例,通过对颈动脉体肿瘤手术标本进行组织学检查、包括间碘苄胍闪烁显像在内的多模态成像以及琥珀酸脱氢酶基因的遗传分析进行评估。最终诊断为颈动脉体和心包的1型PGL。>