CYTOGENETIC ABNORMALITIES IN PRIMARY BRONCHOPULMONARY LEIOMYOSARCOMA OF CHILDHOOD

Citation
Bf. Schneider et al., CYTOGENETIC ABNORMALITIES IN PRIMARY BRONCHOPULMONARY LEIOMYOSARCOMA OF CHILDHOOD, Cancer genetics and cytogenetics, 105(2), 1998, pp. 145-151
Citations number
33
Categorie Soggetti
Oncology,"Genetics & Heredity
ISSN journal
01654608
Volume
105
Issue
2
Year of publication
1998
Pages
145 - 151
Database
ISI
SICI code
0165-4608(1998)105:2<145:CAIPBL>2.0.ZU;2-B
Abstract
Primary bronchopulmonary leiomyosarcoma (PBLMS) is a rare malignant ne oplasm in all age groups and only 10 pediatric cases of PBLMS have bee n reported. This report presents cytogenetic findings of a PBLMS from an 8-year-old boy. Tumor diagnosis was established by using routine hi stopathology, immunohistochemistry, and electron microscopy. The karyo type was highly complex, demonstrating consistent structural abnormali ties of chromosomes 1, 5, 6, and 7, relative gain of chromosomes 2 and 11, and relative loss of chromosomes 9, 19, 20, and 22, along with th e presence of multiple marker chromosomes. Cytogenetic results of prev iously reported leiomyosarcomas are reviewed and compared with the pre sent case. (C) Elsevier Science Inc., 1998