Department of Radiology & Diagnostic Imaging, University of Alberta Hospital, 2A2.41 Walter Mackenzie Centre, 8440-112 St, Edmonton, AB, T6G 2B7, Canada.
AJR Am J Roentgenol. 2013 Feb;200(2):370-8. doi: 10.2214/AJR.12.9126.
Pheochromocytomas are relatively rare neuroendocrine tumors of the adrenal medulla. Their variable clinical presentation and biologic behavior often make accurate diagnosis challenging. A variable spectrum of imaging appearances--some of which may also mimic other diseases--has been recognized. This article reviews the epidemiology; associations; and clinical, biochemical, pathologic, and multimodality imaging features of pheochromocytomas including diagnostic pearls and pitfalls.
Pheochromocytomas are often considered the great mimicker of other adrenal tumors. Because of their varied clinical, imaging, and pathologic appearances, accurate diagnosis can be challenging. The various imaging appearances on ultrasound, CT, MRI, and functional imaging can be complementary and have features that are useful for differentiating pheochromocytoma from other lesions of the adrenal.
嗜铬细胞瘤是肾上腺髓质相对罕见的神经内分泌肿瘤。其多变的临床表现和生物学行为常常使准确诊断具有挑战性。已经认识到了一系列可变的影像学表现,其中一些可能也类似于其他疾病。本文回顾了嗜铬细胞瘤的流行病学;相关性;以及临床、生化、病理和多模态成像特征,包括诊断要点和陷阱。
嗜铬细胞瘤通常被认为是其他肾上腺肿瘤的“伪装大师”。由于其多变的临床、影像和病理表现,准确诊断具有挑战性。超声、CT、MRI 和功能成像上的各种影像学表现是互补的,具有区分嗜铬细胞瘤与肾上腺其他病变的有用特征。