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囊性嗜铬细胞瘤的磁共振成像表现

MR demonstration of a cystic pheochromocytoma.

作者信息

Belden C J, Powers C, Ros P R

机构信息

Department of Radiology, University of Florida College of Medicine, Gainesville 32610-0374, USA.

出版信息

J Magn Reson Imaging. 1995 Nov-Dec;5(6):778-80. doi: 10.1002/jmri.1880050627.

Abstract

Cystic pheochromocytoma is a rare tumor of the adrenal gland that can pose a diagnostic challenge. We report a case of a 14-year-old boy who had an adrenal lesion that appeared cystic by both sonography and CT, but that demonstrated hemorrhage into the lesion at MR imaging, and proved to be a cystic pheochromocytoma. We emphasize the importance of considering the diagnosis of pheochromocytoma when faced with a cystic lesion of the adrenal gland.

摘要

囊性嗜铬细胞瘤是一种罕见的肾上腺肿瘤,会带来诊断挑战。我们报告一例14岁男孩,其肾上腺病变在超声和CT检查中均显示为囊性,但在磁共振成像中显示病变内有出血,最终证实为囊性嗜铬细胞瘤。我们强调,面对肾上腺囊性病变时,考虑嗜铬细胞瘤诊断的重要性。

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MR demonstration of a cystic pheochromocytoma.囊性嗜铬细胞瘤的磁共振成像表现
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