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Congenital mesoblastic nephroma, nephrocalcinosis, and hypertrophic pyloric stenosis

✍ Scribed by Javier C. Angulo; Jose I. Lopez; Cosme Ereñao; Nicolas Flores

Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
373 KB
Volume
48
Category
Article
ISSN
0022-4790

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✦ Synopsis

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.

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Congenital mesoblastic nephroma, although rare, represents the most common renal neoplasm diagnosed in the early postnatal period ( 1 3 ) . More than 70 cases of this benign tumor have been reported (4); however, there are few descriptions in the radiology literature (5-9). Previous reports have em