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腰椎管副神经节瘤——病例报告

Paraganglioma of the lumbar spinal canal -- case report.

作者信息

Słowiński Jerzy, Stomal Monika, Bierzyńska-Macyszyn Grazyna, Swider Kazimierz

机构信息

Department of Neurosurgery and Neurotraumatology, Al. Legionów 10, 41-902 Bytom, Poland.

出版信息

Folia Neuropathol. 2005;43(2):119-22.

Abstract

We present the case of a 46-year-old female with a lumbar spine paraganglioma. The patient complained of a right-sided lumboischialgia. Preoperative MRI revealed an intradural tumour at the vertebra L3 level, located in the midline, 7 mm in diameter. The tumour was totally removed by laminectomy. Histopathological examination showed nests of chief cells (zellballen), surrounded by reticulin fibres. Immunohistochemistry showed a positive reaction for chromogranin A, neuronal specific protein, synaptophysin and cytokeratin in the chief cells. The sustentacular cells displayed immunopositivity for S-100 protein, single cells were also positive for GFAP. We found no proliferative activity in the tumour cells (Ki-67 index = 0%). In the two years follow-up the patient remains without clinical or radiological signs of recurrence. Spinal paraganglioma is a rare, surgically curable tumour with low proliferative potential. This entity should be taken into consideration in the differential diagnosis of extramedullary spinal lesions.

摘要

我们报告一例46岁患有腰椎副神经节瘤的女性病例。患者主诉右侧腰腿痛。术前MRI显示L3椎体水平硬膜内有一肿瘤,位于中线,直径7毫米。通过椎板切除术将肿瘤完全切除。组织病理学检查显示主细胞巢(嗜铬细胞瘤细胞巢),周围有网状纤维。免疫组织化学显示主细胞中嗜铬粒蛋白A、神经元特异性蛋白、突触素和细胞角蛋白呈阳性反应。支持细胞对S-100蛋白呈免疫阳性,单个细胞对GFAP也呈阳性。我们在肿瘤细胞中未发现增殖活性(Ki-67指数=0%)。在两年的随访中,患者没有复发的临床或影像学迹象。脊髓副神经节瘤是一种罕见的、手术可治愈的肿瘤,增殖潜能低。在髓外脊髓病变的鉴别诊断中应考虑到这一实体。

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