Literature DB >> 9722247

Wilms' tumour in infancy.

C M Kullendorff1, T Wiebe.   

Abstract

During a 15-y period, 48 children were treated for Wilms' tumour (WT). Seven of them were < 1 y of age at diagnosis. One child presented with non-traumatic haematuria, but in all the other children WT was revealed as a palpable abdominal mass at routine examination or investigation due to another disease. The four children under 6 months of age at diagnosis were primarily operated upon; the others received preoperative chemotherapy. Two children had chromosomal aberrations in the WT tumour specimen. The follow-up revealed that postoperatively six children are healthy with no evidence of relapse from WT, but one child had a contralateral relapse successfully enucleated. The clinical behaviour and management of WT in infants differ compared with that in older children. The diagnosis may be uncertain and it can be difficult to distinguish between malignant and non-malignant lesions. It is essential to realize the possibility of WT, even in children < 1 y of age.

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Year:  1998        PMID: 9722247     DOI: 10.1080/080352598750013824

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN: 0803-5253            Impact factor:   2.299


  3 in total

1.  Clinicopathological profile of Wilms' tumor.

Authors:  L Paul; D Thaver; S Muzaffar; I N Soomro; Z Nazir; S H Hasan
Journal:  Indian J Pediatr       Date:  2000-10       Impact factor: 1.967

2.  Aniridia and Wilm's tumor.

Authors:  Manisha Nada; K N Rattan; Sarita Magu; Sanjeev Parshad
Journal:  Indian J Pediatr       Date:  2003-10       Impact factor: 1.967

3.  A rare occurrence of neonatal nephroblastoma in sub-saharan Africa: a case report and management in a resource-constrained region.

Authors:  Féfé Khuabi Matondo; Aléine Nzazi Budiongo; Bruno Muyala Tady; Bienvenu Massamba Lebwaze; Michel Tshikwela Lelo; Jean Lambert Gini-Ehungu; Idesbald Mwepu; Emmanuel Dimbu Nkidiaka; Michel Ntetani Aloni
Journal:  Rare Tumors       Date:  2015-03-26
  3 in total

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