Vogler C A, Sotelo-Avila C, Ramón-García G, Salinas-Madrigal L
Department of Pathology, Cardinal Glennon Children's Hospital, St Louis, MO 63104.
Semin Diagn Pathol. 1988 Feb;5(1):122-31.
In a retrospective review, we identified a variety of abnormal immature and differentiated metanephric tissues including nodular renal blastema and metanephric hamartomas in 12 children with urinary tract malformations with or without renal dysplasia. Four infants also had trisomy. Nodular renal blastema was characterized by small subcapsular clusters of primitive metanephric cells, in some cases with evidence of tubular, papillary, or trabecular differentiation. Metanephric hamartomas included papillary adenomas and tubular hamartomas. Undifferentiated renal blastema was multifocal, but more differentiated blastema usually occurred as isolated nodules. When accompanied by renal dysplasia, blastema tended to show differentiation. One child had a spectrum of lesions with both blastema and more differentiated metanephric hamartomas.
在一项回顾性研究中,我们在12例患有或未患有肾发育不全的泌尿系统畸形儿童中,发现了多种异常的未成熟和分化的后肾组织,包括结节性肾胚基和后肾错构瘤。4名婴儿还患有三体综合征。结节性肾胚基的特征是原始后肾细胞的小囊下簇,在某些情况下有肾小管、乳头或小梁分化的证据。后肾错构瘤包括乳头状腺瘤和肾小管错构瘤。未分化的肾胚基是多灶性的,但分化程度更高的胚基通常表现为孤立结节。当伴有肾发育不全时,胚基倾向于显示分化。一名儿童有一系列病变,包括胚基和分化程度更高的后肾错构瘤。