Yazaki T, Akimoto M, Tsuboi N, Kawai H, Miyamoto M, Suzuki T
Urology. 1982 Oct;20(4):446-50. doi: 10.1016/0090-4295(82)90480-0.
For more than a decade congenital mesoblastic nephroma of infancy has been recognized as an entity different from Wilms tumor in its clinical and histopathologic features. However, this tumor is sometimes confused with Wilms tumor and consequently, inadvertent and vigorous therapy compatible with that for Wilms tumor is given. we reviewed the literature and analyzed 90 cases of congenital mesoblastic nephroma in the English and Japanese literature. The importance of early and accurate histopathologic diagnosis of the resected specimen to avoid inappropriate post-operative therapy is emphasized, and the peculiar features of congenital mesoblastic nephroma are characterized.
十多年来，婴儿先天性中胚层肾瘤在临床和组织病理学特征上被认为是一种不同于肾母细胞瘤的实体。然而，这种肿瘤有时会与肾母细胞瘤混淆，因此会给予与肾母细胞瘤治疗相适应的不当且积极的治疗。我们回顾了文献，并分析了英文和日文中90例先天性中胚层肾瘤的病例。强调了对切除标本进行早期准确的组织病理学诊断以避免不适当的术后治疗的重要性，并描述了先天性中胚层肾瘤的独特特征。
