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先天性中胚层肾瘤、肾钙质沉着症和肥厚性幽门狭窄。

Congenital mesoblastic nephroma, nephrocalcinosis, and hypertrophic pyloric stenosis.

作者信息

Angulo J C, López J I, Ereño C, Flores N

机构信息

Servicio de Urología, Santo Hospital Civil de Bilbao, Spain.

出版信息

J Surg Oncol. 1991 Oct;48(2):142-4. doi: 10.1002/jso.2930480214.

Abstract

A cellular variant of congenital mesoblastic nephroma (CMN) occurring in a newborn is presented. Coincidental findings were congenital hypertrophic pyloric stenosis (CHPS) and nephrocalcinotic hypercalcemia that reverted after nephrectomy. As of the day of writing, this multiple association has not been reported. The authors believe that both CMN and CHPS could be interpreted as fibroblastic proliferative-related entities. Transient hypercalcemia seems to be a paraneoplastic phenomenon.

摘要

本文报道了1例发生于新生儿的先天性中胚层肾瘤(CMN)细胞变异型。巧合的是,还发现了先天性肥厚性幽门狭窄(CHPS)和肾钙质沉着性高钙血症,肾切除术后高钙血症得以恢复。截至撰写本文时,这种多重关联尚未见报道。作者认为,CMN和CHPS都可被解释为与成纤维细胞增殖相关的实体。短暂性高钙血症似乎是一种副肿瘤现象。

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