首页> 外文期刊>Neuropathology: official journal of the Japanese Society of Neuropathology >Desmoplastic infantile ganglioglioma with focal cortical dysplasia: A rare double pathology in an infant with history of seizures
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Desmoplastic infantile ganglioglioma with focal cortical dysplasia: A rare double pathology in an infant with history of seizures

机译:增生性小儿神经节神经胶质瘤伴局灶性皮质发育不良:患有癫痫病史的婴儿罕见的双重病理

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摘要

We describe an extremely rare case of double pathology arising in an infant girl presenting with a history of intractable seizures, delayedmilestones and enlarging head. The pathology included desmoplastic infantile ganglioglioma (DIG) and extensive focal cortical dysplasia in the overlying cortex. While tumors such as ganglioglioma have been commonly described to occur as concomitant pathology with cortical dysplasia, DIG in such an association has not been described in the literature. As DIG are voluminous supratentorial tumors, awareness about such an association is pertinent for correct diagnosis.
机译:我们描述了一个极其罕见的双重病理情况,该情况是由于一名女婴出现了顽固性癫痫,里程碑延迟和头颅增大的病史。病理包括增生性婴儿神经节神经胶质瘤(DIG)和上皮皮质广泛的局灶性皮质发育异常。虽然通常已将诸如神经节神经胶质瘤的肿瘤描述为伴有皮质发育异常的病理,但文献中尚未描述这种关联的DIG。由于DIG是大量的幕上肿瘤,因此对于正确诊断具有相关性的认识。

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