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心脏嗜铬细胞瘤。一例病例报告及文献综述。

Cardiac pheochromocytoma. A case report and review of the literature.

作者信息

Gomi T, Ikeda T, Sakurai J, Toya Y, Tani M

机构信息

Department of Nephrology, Kanto-Teishin Hospital, Tokyo, Japan.

出版信息

Jpn Heart J. 1994 Jan;35(1):117-24. doi: 10.1536/ihj.35.117.

Abstract

A case of intrapericardial pheochromocytoma which secreted predominantly norepinephrine is reported. A tumor at the posterior wall of the left atrium was demonstrated by computed tomographic and magnetic resonance imaging scan. Tumor blush arising from the left circumflex branch was visualized by coronary angiography. The tumor (4 x 3.5 x 2 cm) was resected with adherent atrial wall and the defect reconstructed with the patients own pericardium under general anesthesia with artificial cardiopulmonary bypass. His subsequent postoperative recovery was uneventful. At the time of discharge, 8 weeks after operation, his blood pressure and plasma norepinephrine remained normal. The value of magnetic resonance imaging scan for the topographic diagnosis of cardiac pheochromocytoma is emphasized.

摘要

报告了一例主要分泌去甲肾上腺素的心包内嗜铬细胞瘤。计算机断层扫描和磁共振成像扫描显示左心房后壁有一个肿瘤。冠状动脉造影显示左旋支出现肿瘤性造影剂充盈。在全身麻醉和人工心肺旁路下,将肿瘤(4×3.5×2厘米)与粘连的心房壁一并切除,缺损用患者自身心包重建。患者术后恢复顺利。术后8周出院时,其血压和血浆去甲肾上腺素仍保持正常。强调了磁共振成像扫描对心脏嗜铬细胞瘤进行地形学诊断的价值。

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