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Unusual central nervous system presentation of ALK-positive anaplastic large cell lymphoma in a child

机译:儿童ALK阳性间变性大细胞淋巴瘤的异常中枢神经系统表现

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An 11-year-old boy landed in emergency in a semiconscious state with a history of headache, generalised tonic-clonic seizures and vomiting of 6 months duration. On examination there was no lymphadenopathy or organomegaly. Contrast-enhanced computed tomography (CECT) scan revealed multiple dural based homogenously enhancing lesions along the left side of cavernous sinus, left tentorium, right tentorial edge, and left posterior temporal convexity dura with significant oedema in left tempro-occipital brain [Figure la-c].
机译:一名11岁男孩在半昏迷状态下紧急进入,有头痛史,全身性强直阵挛性癫痫发作和持续6个月的呕吐。经检查没有淋巴结肿大或器质性肿大。对比增强计算机断层扫描(CECT)扫描显示,沿海绵窦,左腱鞘,右腱膜边缘和左后颞凸硬脑膜左侧有多个基于硬脑膜的均匀增强病变,左颞枕脑明显水肿[图la- C]。

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