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首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >Renal cell carcinoma to haemangioblastoma metastasis: A rare manifestation of Von Hippel-Lindau syndrome
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Renal cell carcinoma to haemangioblastoma metastasis: A rare manifestation of Von Hippel-Lindau syndrome

机译:肾细胞癌成血管母细胞瘤转移:冯·Hippel-Lindau综合征的罕见表现

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摘要

Brain metastases are the most common intracranial malignancy in adults and may occasionally deposit within a pre-existing primary brain neoplasm. We describe, in two directly related family members, the rare occurrence of renal cell carcinoma (RCC) metastasis to haemangioblastoma (HB) in the context of Von Hippel Lindau syndrome. Detection of this phenomenon can be marred by histological overlap between RCC and HB and therefore careful histological examination, and consideration of supportive immunohistochemistry, is required when examining all HB resections. Metastatic RCC to HB upstages a primary RCC and is clinically diagnostic of Von Hippel Lindau syndrome. (C) 2014 Elsevier Ltd. All rights reserved.
机译:脑转移瘤是成人中最常见的颅内恶性肿瘤,偶尔可能沉积在已存在的原发性脑肿瘤内。我们在两个直接相关的家庭成员中描述了在Von Hippel Lindau综合征的背景下,肾细胞癌(RCC)转移至血管母细胞瘤(HB)的罕见情况。 RCC和HB之间的组织学重叠可能会损害这种现象的检测,因此在检查所有HB切除物时,需要仔细进行组织学检查,并考虑支持性免疫组织化学。转移至HB的RCC较原发性RCC提早了,并且在临床上诊断为Von Hippel Lindau综合征。 (C)2014 Elsevier Ltd.保留所有权利。

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