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多形性黄色星形细胞瘤的临床、影像学及治疗特征:三例报告并文献复习

Clinical, radiological, and therapeutic features of pleomorphic xanthoastrocytoma: report of three patients and review of the literature.

作者信息

van Roost D, Kristof R, Zentner J, Wolf H K, Schramm J

机构信息

Department of Neurosurgery, University of Bonn, Germany.

出版信息

J Neurol Neurosurg Psychiatry. 1996 Jun;60(6):690-2. doi: 10.1136/jnnp.60.6.690.

Abstract

Two out of three patients with pleomorphic xanthoastrocytoma were initially misdiagnosed and correctly interpreted only at tumour recurrence, with progression to malignancy in one. The third patient presented with a remarkably long history of epilepsy. Pleomorphic xanthoastrocytoma is a low grade astrocytoma that is still confused with other tumours. Because pleomorphic xanthoastrocytoma can become malignant even after many years of benign behaviour, a long term follow up is necessary.

摘要

三分之二的多形性黄色星形细胞瘤患者最初被误诊,仅在肿瘤复发时才得到正确诊断,其中一例进展为恶性肿瘤。第三位患者有很长的癫痫病史。多形性黄色星形细胞瘤是一种低级别星形细胞瘤,目前仍易与其他肿瘤混淆。由于多形性黄色星形细胞瘤即使在多年表现为良性之后仍可能恶变,因此需要长期随访。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e3f/1073958/50e844af3dbb/jnnpsyc00018-0092-a.jpg

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