Congenital disseminated malignant rhabdoid tumor: A distinct clinicopathologic entity demonstrating abnormalities of chromosome 22q11

Frances V. White; Louis P. Dehner; Deborah A Belchis; Katrina Conard; Mary M. Davis; J. Thomas Stocker; Craig W. Zuppan; Jaclyn A. Biegel; Elizabeth J. Perlman

doi:10.1097/00000478-199903000-00001

Congenital disseminated malignant rhabdoid tumor: A distinct clinicopathologic entity demonstrating abnormalities of chromosome 22q11

Frances V. White, Louis P. Dehner, Deborah A Belchis, Katrina Conard, Mary M. Davis, J. Thomas Stocker, Craig W. Zuppan, Jaclyn A. Biegel, Elizabeth J. Perlman

Research output: Contribution to journal › Article › peer-review

98 Scopus citations

Abstract

The clinical, pathologic, and immunohistochemical features of a widely disseminated tumor with rhabdoid phenotype are described in nine infants ≤3 months of age. Five neonates had tumor evident at birth, two of which had placental metastases. The average survival following diagnosis was

Original language	English (US)
Pages (from-to)	249-256
Number of pages	8
Journal	American Journal of Surgical Pathology
Volume	23
Issue number	3
DOIs	https://doi.org/10.1097/00000478-199903000-00001
State	Published - Mar 1999
Externally published	Yes

Keywords

Chromosome 22
Congenital tumors
Malignant rhabdoid tumor
Placenta metastasis

ASJC Scopus subject areas

Anatomy
Pathology and Forensic Medicine

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10.1097/00000478-199903000-00001

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White, F. V., Dehner, L. P., Belchis, D. A., Conard, K., Davis, M. M., Stocker, J. T., Zuppan, C. W., Biegel, J. A., & Perlman, E. J. (1999). Congenital disseminated malignant rhabdoid tumor: A distinct clinicopathologic entity demonstrating abnormalities of chromosome 22q11. American Journal of Surgical Pathology, 23(3), 249-256. https://doi.org/10.1097/00000478-199903000-00001

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title = "Congenital disseminated malignant rhabdoid tumor: A distinct clinicopathologic entity demonstrating abnormalities of chromosome 22q11",

abstract = "The clinical, pathologic, and immunohistochemical features of a widely disseminated tumor with rhabdoid phenotype are described in nine infants ≤3 months of age. Five neonates had tumor evident at birth, two of which had placental metastases. The average survival following diagnosis was ",

keywords = "Chromosome 22, Congenital tumors, Malignant rhabdoid tumor, Placenta metastasis",

author = "White, {Frances V.} and Dehner, {Louis P.} and Belchis, {Deborah A} and Katrina Conard and Davis, {Mary M.} and Stocker, {J. Thomas} and Zuppan, {Craig W.} and Biegel, {Jaclyn A.} and Perlman, {Elizabeth J.}",

year = "1999",

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doi = "10.1097/00000478-199903000-00001",

language = "English (US)",

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pages = "249--256",

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T1 - Congenital disseminated malignant rhabdoid tumor

T2 - A distinct clinicopathologic entity demonstrating abnormalities of chromosome 22q11

AU - White, Frances V.

AU - Dehner, Louis P.

AU - Belchis, Deborah A

AU - Conard, Katrina

AU - Davis, Mary M.

AU - Stocker, J. Thomas

AU - Zuppan, Craig W.

AU - Biegel, Jaclyn A.

AU - Perlman, Elizabeth J.

PY - 1999/3

Y1 - 1999/3

N2 - The clinical, pathologic, and immunohistochemical features of a widely disseminated tumor with rhabdoid phenotype are described in nine infants ≤3 months of age. Five neonates had tumor evident at birth, two of which had placental metastases. The average survival following diagnosis was

AB - The clinical, pathologic, and immunohistochemical features of a widely disseminated tumor with rhabdoid phenotype are described in nine infants ≤3 months of age. Five neonates had tumor evident at birth, two of which had placental metastases. The average survival following diagnosis was

KW - Chromosome 22

KW - Congenital tumors

KW - Malignant rhabdoid tumor

KW - Placenta metastasis

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JF - American Journal of Surgical Pathology

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ER -

Congenital disseminated malignant rhabdoid tumor: A distinct clinicopathologic entity demonstrating abnormalities of chromosome 22q11

Abstract

Keywords

ASJC Scopus subject areas

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