Marsden H B, Lawler W
Br J Cancer. 1978 Sep;38(3):437-41. doi: 10.1038/bjc.1978.226.
A primary renal tumour of childhood with histological appearances different from the nephroblastoma is described. This neoplasm, predominantly seen in boys, has a tendency to metastasize to bone. Such metastases are considered to be rare in nephroblastoma and this aspect in studies of Wilms' tumour series is thought to be due, for the most part, to the inclusion of a particular bone-metastasizing tumour in the material.
本文描述了一种组织学表现不同于肾母细胞瘤的儿童原发性肾肿瘤。这种肿瘤主要见于男孩,有转移至骨的倾向。在肾母细胞瘤中,这种转移被认为是罕见的,在威尔姆斯瘤系列研究中,这方面情况在很大程度上被认为是由于研究材料中包含了一种特定的骨转移性肿瘤。