Wang Zhe-Hui, Wang Yuan-Tao, Cheng Fei, Hu Yu
Department of Pathology, China-Japan Union Hospital of Jilin University.
Department of Urology, The First Hospital of Jilin University, Changchun, Jilin.
Medicine (Baltimore). 2018 Oct;97(41):e12586. doi: 10.1097/MD.0000000000012586.
This study aims to investigate the pathological features of a patient with paraganglioma in the lumbar spinal canal.
The patient was 36 years old male with electrical pain in the waist and buttock which occurred intermittently, and was not relieved under oral use of analgesics. Immunohistochemical staining was performed to diagnose the disease. The results revealed that the size of the tumor was 3.4 × 1.6 × 1.4 cm. The hematoxylin and eosin (H&E)-stained tumor cells mainly presented with an organ-like arrangement under low power microscope, showing prominent chrysanthemum-like, pseudo glandular or pseudo papillary arrangements. The surrounding area of the nest presented with sinusoids, and fibrosis and focal calcification could be observed in the interstitial space among the lesions. Immunohistochemistry results showed that the chief cells were positive for neuron-specific enolase (NSE), Syn and CgA, and Sertoli cells were positive for S-100.
Paraganglioma is a very rare malignant tumor. This tumor should be distinguished from ependymoma, meningioma and hemangioblastoma, to avoid misdiagnosis, and missed diagnosis.
本研究旨在探讨一名腰椎管副神经节瘤患者的病理特征。
患者为36岁男性,腰部和臀部间歇性出现电击样疼痛,口服镇痛药后未缓解。通过免疫组织化学染色对疾病进行诊断。结果显示肿瘤大小为3.4×1.6×1.4厘米。苏木精-伊红(H&E)染色的肿瘤细胞在低倍显微镜下主要呈器官样排列,可见明显的菊花样、假腺管样或假乳头样排列。巢周区域可见血窦,病变间的间质可见纤维化和局灶性钙化。免疫组织化学结果显示,主细胞神经元特异性烯醇化酶(NSE)、突触素(Syn)和嗜铬粒蛋白A(CgA)呈阳性,支持细胞S-100呈阳性。
副神经节瘤是一种非常罕见的恶性肿瘤。该肿瘤应与室管膜瘤、脑膜瘤和血管母细胞瘤相鉴别,以避免误诊和漏诊。