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作 者:Lei-Ming Wang Meng Zhang Pei-Pei Wang Xin-Gang Zhou Yue-Shan Piao De-Hong Lu
机构地区:[1]Department of Pathology,Xuanwu Hospital,Capital Medical University,Beijing 100053,China [2]Department of Radiology,Xuanwu Hospital,Capital Medical University,Beijing 100053,China [3]Department of Pathology,Beijing Ditan Hospital,Capital Medical University,Beijing 100015,China
出 处:《Chinese Medical Journal》2019年第20期2495-2497,共3页中华医学杂志(英文版)
摘 要:To the Editor: The Dandy-Walker malformation (DWM) is a rare congenital malformation involving the posterior fossa. Diagnosis of the DWM is based on a series of characteristic neuroimaging findings, which include complete or partial agenesis of the cerebellar vermis, cystic dilatation of the fourth ventricle, and enlarged posterior fossa.[1] Several malformation syndromes and cytogenetic abnormalities have been associated with the DWM. However, the co-existence of the DWM and neoplasms is rare.[2] There are rare reports of the co-existence of the DWM and ganglioglioma.
关 键 词:MALFORMATION NEOPLASMS GLIOMA
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