Svajdler M ml, Bohus P, Závacký P, Vol'anská M, Repovský A, Juskanicová E
Department of Pathology, Louis Pasteur Faculty Hospital, Kosice.
Cesk Patol. 2007 Oct;43(4):153-6.
Extra-adrenal paragangliomas constitute 10 % or less of phaeochromocytomas/paragangliomas. Even rarer is the occurrence of paragangliomas outside the usual distribution of paraganglionic tissue. We report a case of extra-adrenal paraganglioma occurring in the small intestine mesentery in a 65-year-old man. To our knowledge, there are only seven case reports of paraganglioma occurring in this non-typical site. Computed tomography showed a solid expansive non-homogenously enhancing mesenteric mass, measuring 10 x 8 cm with peripheral cystic component. Histologically, the tumour had a typical organoid "zellballen" pattern, showed immunohistochemical positivity for synaptophysin, neuron specific enolase, CD-56, chromogranin, and focally vimentin, and was cytokeratin and EMA negative. S-100 protein stained few sustentacular cells. The patient was free from recurrence or metastasis three months after tumour resection. Although rare, paraganglioma should be included in the preoperative differential diagnosis of solid mesenteric tumours, to prevent any potential life-threatening event peroperatively in the case of a catecholamines-producing tumour.
肾上腺外副神经节瘤占嗜铬细胞瘤/副神经节瘤的比例为10%或更低。副神经节瘤出现在副神经节组织通常分布范围之外的情况更为罕见。我们报告一例发生在一名65岁男性小肠系膜的肾上腺外副神经节瘤。据我们所知,仅有7例关于副神经节瘤发生在这个非典型部位的病例报告。计算机断层扫描显示一个实性、膨胀性、不均匀强化的肠系膜肿块,大小为10×8 cm,周边有囊性成分。组织学上,肿瘤具有典型的类器官样“细胞巢”模式,突触素、神经元特异性烯醇化酶、CD-56、嗜铬粒蛋白以及局灶性波形蛋白免疫组化呈阳性,细胞角蛋白和上皮膜抗原阴性。S-100蛋白仅对少数支持细胞染色。肿瘤切除术后三个月,患者无复发或转移。尽管罕见,但副神经节瘤应纳入肠系膜实性肿瘤的术前鉴别诊断,以防止在肿瘤产生儿茶酚胺的情况下术中出现任何潜在的危及生命的情况。