Antoniou Dimitrios, Papatheodorou Harabos, Ziras Nikolaos, Zizi-Serbetzoglou Adamantia, Paschalidis Nikolaos, Christopoulou Agapi, Filippakou Ekaterini, Trivizaki Erasmia
Department of Nuclear Medicine, "Metaxa" Cancer Hospital, 51 Botassi Str., 185 37 Piraeus, Greece.
Hell J Nucl Med. 2011 May-Aug;14(2):163-5.
Paragangliomas, also described as ectopic pheochromocytomas are infrequent neuroectodermal neoplasms that could be found wherever paraganglionic tissue exists. We present a rare case of a manifold non-functional primary hepatic paraganglioma in a 71 years old female. The combination of structural computed tomography and magnetic resonance imaging and of a functional modality, octreotide scan supported diagnosis. The role of nuclear medicine is crucial because it may help to determine future treatment in cases where there is suspicion of this tumour. However it has certain limitations, largely related to the physiological radionuclidic biodistribution. This case is described because of its relative rarity and also to emphasize the need to be studied by multidisciplinary collaboration.
副神经节瘤,也被描述为异位嗜铬细胞瘤,是罕见的神经外胚层肿瘤,可在副神经节组织存在的任何部位发现。我们报告一例71岁女性多发无功能原发性肝副神经节瘤的罕见病例。结构计算机断层扫描、磁共振成像以及功能检查奥曲肽扫描相结合有助于诊断。核医学的作用至关重要,因为在怀疑存在这种肿瘤的情况下,它可能有助于确定未来的治疗方案。然而,它有一定的局限性,主要与生理性放射性核素生物分布有关。描述该病例是因为其相对罕见,同时也强调了多学科合作研究的必要性。