Document Detail


Germ cell tumours in neonates and infants: a distinct subgroup?
MedLine Citation:
PMID:  12752256     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Human germ cell tumours (GCTs) constitute a heterogeneous group of tumours that can be classified into four major subgroups. One of these subgroups encompasses (immature) teratomas and yolk sac tumours of patients under the age of 5 years. In this paper we review the various clinical, histological and cytogenetical aspects of these infantile GCTs. The primordial germ cell (PGC) has been suggested to be the cell of origin for GCTs. Infantile GCTs, however, have been suggested to originate from PGCs at a different stage of maturation than adult GCTs. The cytogenetic constitution of infantile GCTs also appears to differ from the adult GCTs and includes recurrent losses of lp and 6q. Recently, two cases of infantile GCT were detected with constitutional 12q13 translocations. These exceptional cases may be instrumental in the search for candidate genes related to infantile and/or adult GCT development.
Authors:
Imke M Veltman; Marga T Schepens; Leendert H J Looijenga; Louise C Strong; Ad Geurts van Kessel
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Review    
Journal Detail:
Title:  APMIS : acta pathologica, microbiologica, et immunologica Scandinavica     Volume:  111     ISSN:  0903-4641     ISO Abbreviation:  APMIS     Publication Date:  2003 Jan 
Date Detail:
Created Date:  2003-05-19     Completed Date:  2003-06-24     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  8803400     Medline TA:  APMIS     Country:  Denmark    
Other Details:
Languages:  eng     Pagination:  152-60; discussion 160     Citation Subset:  IM    
Affiliation:
Department of Human Genetics, University Medical Center Nijmegen, Nijmegen, The Netherlands. i.veltman@antrg.UMCN.nl
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MeSH Terms
Descriptor/Qualifier:
Chromosome Aberrations
Chromosome Mapping
Chromosomes, Human, Pair 12
Germinoma / epidemiology,  pathology*
Humans
Infant
Infant, Newborn
Karyotyping
Male
Sacrococcygeal Region*
Teratoma / epidemiology,  genetics,  pathology*
Translocation, Genetic

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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