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青少年原发性脊髓促结缔组织增生性星形细胞瘤:罕见部位、罕见年龄的罕见肿瘤。

Primary spinal cord desmoplastic astrocytoma in an adolescent: a rare tumour at rare site and rare age.

机构信息

Department of Imaging and Interventional Radiology, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong.

出版信息

Hong Kong Med J. 2012 Jun;18(3):253-5.

Abstract

We report a case of a non-infantile primary intramedullary spinal cord desmoplastic astrocytoma in an 18-year-old girl who presented with spastic paraparesis. The patient had been unable to run for 1 year. Magnetic resonance imaging of her spine showed an intramedullary solid and cystic heterogeneously enhancing lesion located at T7-T8 level. Partial excision was performed. Histology revealed a desmoplastic astrocytoma. To the best of our knowledge, there is no report on primary desmoplastic astrocytoma of the spinal cord in literature. Nor has such a symptomatic tumour manifesting at the age of 18 years been documented.

摘要

我们报告了一例 18 岁女孩的非婴儿型原发性脊髓髓内硬纤维瘤样星形细胞瘤,该患者表现为痉挛性截瘫。患者 1 年来无法跑步。脊柱磁共振成像显示 T7-T8 水平的髓内实性和囊性不均匀强化病变。进行了部分切除。组织学显示为硬纤维瘤样星形细胞瘤。据我们所知,文献中尚无脊髓原发性硬纤维瘤样星形细胞瘤的报道。也没有记录到这种症状性肿瘤在 18 岁时出现。

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