Crozier F, Lechevallier E, Eghazarian C, André M, Sammama D, Wilshire P, Vidal V, Pascal P, Bartoli J M
Service de Radiologie générale, Hôpital de la Timone, Marseille.
J Radiol. 1999 Feb;80(2):150-2.
Paraganglioma is a rare tumor arising from indifferentiated cells of the primitive neural crest. These tumors are most commonly found in the adrenal gland but other localisations are possible. We described a 60-year-old men with a right retro-peritoneal mass discovered on ultrasound examination. This tumor had an heterogeneous appearance on i.v. contrast injected CT (computed tomography) and MR (magnetic resonance) images. Plasma and urinary catecholamines were normal. This tumor was surgically removed. Immunohistochemical analyses revealed that the tumor cells were strongly positive for neurone specific enolase and chromogranin A. Histopathologic examination diagnosed a non secreting paraganglioma in the right retroperitoneum. After surgery, the patient remained asymptomatic without treatment.
副神经节瘤是一种起源于原始神经嵴未分化细胞的罕见肿瘤。这些肿瘤最常见于肾上腺,但也可能出现在其他部位。我们描述了一名60岁男性,超声检查发现右腹膜后肿块。该肿瘤在静脉注射造影剂的CT(计算机断层扫描)和MR(磁共振)图像上表现为不均匀。血浆和尿儿茶酚胺正常。该肿瘤经手术切除。免疫组织化学分析显示肿瘤细胞神经元特异性烯醇化酶和嗜铬粒蛋白A呈强阳性。组织病理学检查诊断为右腹膜后非分泌性副神经节瘤。手术后,患者未经治疗仍无症状。