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心脏合并肾上腺多发嗜铬细胞瘤。

Heart combined with adrenal multiple pheochromocytomas.

机构信息

Department of Cardiology, The Second Affiliated Hospital of Harbin Medical University, No. 246 Xuefu Road, Harbin, Heilongjiang Province, China.

出版信息

J Nucl Cardiol. 2018 Jun;25(3):1040-1043. doi: 10.1007/s12350-017-0860-9. Epub 2017 Jun 7.

Abstract

Pheochromocytoma is a kind of rare tumor, occurring at any site in the sympathoadrenal system. Main lesions occur within the adrenal gland; only 1%-2% occur within the chest, and most of these are located in the posterior mediastinum. Intrapericardial pheochromocytoma is extremely rare in clinic, only about 100 cases have been reported in total in both the domestic and foreignliterature since Besterman et al. first reported in 1974. It is often difficult to diagnose and locate these tumors. Hence, we present here a case of adrenal combined with heart multiple pheochromocytomas and discuss about techniques contributed to diagnosis and localization.

摘要

嗜铬细胞瘤是一种罕见的肿瘤,可发生于交感肾上腺系统的任何部位。主要病变发生于肾上腺;仅 1%-2%发生于胸部,其中大多数位于后纵隔。心包内嗜铬细胞瘤在临床上极为罕见,自 1974 年 Besterman 等人首次报道以来,国内外文献中总共报道了约 100 例。这些肿瘤的诊断和定位往往很困难。因此,我们在此报告一例肾上腺合并心脏多发嗜铬细胞瘤,并讨论有助于诊断和定位的技术。

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