Wilms tumor, AML and medulloblastoma in a child with cancer prone syndrome of total premature chromatid separation and Fanconi anemia.

Abstract:

:Wilms tumor (WT) is the most common primary renal tumor in childhood. The occurrence of WT in patients with growth retardation, mental retardation and central nervous system abnormalities in association with premature chromatid separation (PCS) and mosaic variegated aneuploidy has been previously described in only 10 patients. Here we report the very rare occurrence of WT with two other malignancies, acute myeloid leukemia and medulloblastoma in association with chromosomal instability. This is a novel presentation of Fanconi anemia with this cytogenetic abnormality.

journal_name

Pediatr Blood Cancer

journal_title

Pediatric blood & cancer

authors

Sari N,Akyuz C,Aktas D,Gumruk F,Orhan D,Alikasifoglu M,Aydin B,Alanay Y,Buyukpamukcu M

doi

10.1002/pbc.21966

subject

Has Abstract

pub_date

2009-08-01 00:00:00

pages

208-10

issue

2

eissn

1545-5009

issn

1545-5017

journal_volume

53

pub_type

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