Literature DB >> 8998536

[Wilms tumor and Bloom syndrome].

C Berger1, D Frappaz, D Leroux, F Blez, M Vercherat, E Bouffet, P Jalbert, M Brunat-Mentigny.   

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. 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.
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.

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Year:  1996        PMID: 8998536     DOI: 10.1016/0929-693x(96)82165-8

Source DB:  PubMed          Journal:  Arch Pediatr        ISSN: 0929-693X            Impact factor:   1.180


  3 in total

Review 1.  Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour.

Authors:  R H Scott; C A Stiller; L Walker; N Rahman
Journal:  J Med Genet       Date:  2006-05-11       Impact factor: 6.318

2.  Diagnosis of Bloom Syndrome in a Patient with Short Stature, Recurrence of Malignant Lymphoma, and Consanguineous Origin.

Authors:  Jakub Trizuljak; Terezie Petruchová; Ivona Blaháková; Zuzana Vrzalová; Věra Hořínová; Martina Doubková; Jozef Michalka; Jiří Mayer; Šárka Pospíšilová; Michael Doubek
Journal:  Mol Syndromol       Date:  2020-03-21

3.  Discrepant outcomes in two Brazilian patients with Bloom syndrome and Wilms' tumor: two case reports.

Authors:  Marilia Borges Moreira; Caio Robledo Dc Quaio; Aline Cristina Zandoná-Teixeira; Gil Monteiro Novo-Filho; Evelin Aline Zanardo; Leslie Domenici Kulikowski; Chong Ae Kim
Journal:  J Med Case Rep       Date:  2013-12-30
  3 in total

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