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

作者信息

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

机构信息

Department of Pathology, IWK Children's Hospital, Halifax, Nova Scotia, Canada.

出版信息

Pediatr Pathol. 1991 Jan-Feb;11(1):131-42. doi: 10.3109/15513819109064749.

DOI:10.3109/15513819109064749
PMID: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.

摘要

相似文献

1
Congenital hepatoblastoma and Beckwith-Wiedemann syndrome: a case study including DNA ploidy profiles of tumor and adrenal cytomegaly.
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2
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Congenital Hepatoblastoma and Beckwith-Wiedemann Syndrome.先天性肝母细胞瘤与贝克威思-威德曼综合征。
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Adrenal masses associated with Beckwith Wiedemann syndrome in the newborn.新生儿中与贝克威思-维德曼综合征相关的肾上腺肿块。
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Hepatoblastoma in an infant with Beckwith-Wiedemann Syndrome.患有贝克威思-维德曼综合征的婴儿中的肝母细胞瘤。
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Congenital pancreatoblastoma in Beckwith-Wiedemann syndrome: an emerging association.贝克威思-维德曼综合征中的先天性胰腺母细胞瘤：一种新出现的关联。
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引用本文的文献

1
Neonatal hepatoblastoma in a newborn with severe phenotype of Beckwith-Wiedemann syndrome.新生儿肝母细胞瘤合并 Beckwith-Wiedemann 综合征严重表型一例
Eur J Pediatr. 2011 Nov;170(11):1407-11. doi: 10.1007/s00431-011-1455-0. Epub 2011 Mar 30.
2
Activin induces x-zone apoptosis that inhibits luteinizing hormone-dependent adrenocortical tumor formation in inhibin-deficient mice.激活素诱导X区细胞凋亡，从而抑制促黄体生成素依赖性肾上腺皮质肿瘤在抑制素缺陷小鼠中的形成。
Mol Cell Biol. 2003 Jun;23(11):3951-64. doi: 10.1128/MCB.23.11.3951-3964.2003.
3
The cell type-specific IGF2 expression during early human development correlates to the pattern of overgrowth and neoplasia in the Beckwith-Wiedemann syndrome.
人类早期发育过程中细胞类型特异性的IGF2表达与贝克威思-维德曼综合征中的过度生长和肿瘤形成模式相关。
Am J Pathol. 1994 Oct;145(4):802-17.
4
DNA ploidy abnormalities in the liver of children with hereditary tyrosinemia type I. Correlation with histopathologic features.I型遗传性酪氨酸血症患儿肝脏中的DNA倍体异常。与组织病理学特征的相关性。
Am J Pathol. 1992 May;140(5):1111-9.