Wang Haili, Yao Zhigang, Liu Qingwei
Department of Radiology, Shandong Provincial Hospital affiliated to Shandong University.
Department of Pathology, Shandong Provincial Hospital affiliated to Shandong University.
J Nippon Med Sch. 2018;85(5):297-299. doi: 10.1272/jnms.JNMS.2018_85-48.
Congenital mesoblastic nephroma (CMN) is a rare tumor of infancy. CMNs can be histologically divided into classic, cellular, and mixed subtypes. Cellular CMNs are difficult to differentiate from Wilms tumors. Herein, a neonate with cellular CMN accompanied by macroscopic hematuria, is described. The clinical, pathological, and imaging features of the disease are discussed.
先天性中胚层肾瘤（CMN）是一种罕见的婴儿期肿瘤。CMN在组织学上可分为经典型、细胞型和混合型亚型。细胞型CMN很难与肾母细胞瘤相鉴别。本文描述了一名患有细胞型CMN并伴有肉眼血尿的新生儿。并对该疾病的临床、病理和影像学特征进行了讨论。
