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[Wilms tumor and Bloom syndrome].
- Source :
-
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie [Arch Pediatr] 1996 Aug; Vol. 3 (8), pp. 802-5. - Publication Year :
- 1996
-
Abstract
- Unlabelled: Bloom syndrome is characterized by growth failure, skin anomalies with sun sensitivity, minor anatomic defects, excessive chromosomic fragility and usually severe immune deficiency. The chromosome fragility predisposes these children to the development of hematologic malignancies and solid tumors.<br />Case Report: Morgan, a 4-year-old boy with Bloom syndrome, developed a Wilms tumor. Chemotherapy was poorly tolerated. Two years later, the child died from an uncontrolled progressive disease.<br />Conclusion: This is the fourth reported case of Wilms tumor occurring in a child with Bloom syndrome. This possibility requires repeated abdominal ultrasonography in such patients.
Details
- Language :
- French
- ISSN :
- 0929-693X
- Volume :
- 3
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
- Publication Type :
- Academic Journal
- Accession number :
- 8998536
- Full Text :
- https://doi.org/10.1016/0929-693x(96)82165-8