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Congenital hepatoblastoma and Beckwith-Wiedemann syndrome: a case study including DNA ploidy profiles of tumor and adrenal cytomegaly.

Orozco-Florian, R; McBride, J A; Favara, B E; Steele, A; Brown, S J; Steele, P.

Pediatr Pathol ; 11(1): 131-42, 1991.

Article in English | MEDLINE | ID: mdl-1849635

ABSTRACT

A case of fatal congenital hepatoblastoma is described in which the autopsy provided the first evidence of Beckwith-Wiedemann syndrome. Aneuploid quantitative DNA patterns were found by image analysis of the tumor and the cytomegalic adrenal gland.

Subject(s)

Adrenal Glands/pathology , Beckwith-Wiedemann Syndrome/complications , Carcinoma, Hepatocellular/genetics , DNA/genetics , Liver Neoplasms/genetics , Ploidies , Beckwith-Wiedemann Syndrome/pathology , Carcinoma, Hepatocellular/congenital , Carcinoma, Hepatocellular/pathology , Female , Humans , Infant, Newborn , Liver Neoplasms/congenital , Liver Neoplasms/pathology

ABSTRACT

Subject(s)

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