Literature DB >> 6261033

[Congenital mesoblastic nephroma in infancy--survey of 74 cases with regard to recidivism and therapeutic results (author's transl)].

H Reddemann, G Lorenz, U Rehberg.   

Abstract

The congenital mesoblastic nephroma is clearly distinguishable from Wilms' tumour. Almost exclusively it becomes manifest in early infancy. From the literature 71 established cases were complied, 3 own cases have been added. By many authors this tumour was characterized as benign. There has been, however, a total of 7 recurrences. An epicritical review is given of the course of one own case. The complications arising from radio-and chemotherapy clearly indicate that surgery is the method of choice of semi-malignant tumour.

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Year:  1980        PMID: 6261033     DOI: 10.1055/s-2008-1035635

Source DB:  PubMed          Journal:  Klin Padiatr        ISSN: 0300-8630            Impact factor:   1.349


  1 in total

1.  Abdominal, retroperitoneal and sacrococcygeal tumours of the newborn and the very young infant. Report from the Kiel Paediatric Tumour Registry.

Authors:  D Harms; D Schmidt; I Leuschner
Journal:  Eur J Pediatr       Date:  1989-08       Impact factor: 3.183

  1 in total

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