Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2001-6-26
pubmed:abstractText
Soft tissue sarcomas constitute a heterogeneous group of malignant tumors of mesenchymal origin, the classification of which may present a diagnostic challenge. We present here the cytological, histopathological, immunohistochemical, and cytogenetic findings of an unusual case of a highly aggressive sarcoma. Based on the morphology and the immunohistochemical profile, this primitive tumor and its metastases could not be conclusively classified as any of the defined subtypes of sarcomas, although the findings were suggestive of a variant of rhabdomyosarcoma. Cytogenetic characterization using G-banding, SKY, FISH, and CGH revealed almost identical chromosomal compositions of the primary tumor and the metastasis. The hypertetraploid karyotype was characterized by numerical imbalances as well as by an unbalanced translocation t(1;19)(q12;q13.2), which has not been previously reported.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0165-4608
pubmed:author
pubmed:issnType
Print
pubmed:volume
127
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
128-33
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:11425451-Amputation, pubmed-meshheading:11425451-Biopsy, Needle, pubmed-meshheading:11425451-Chromosome Mapping, pubmed-meshheading:11425451-Chromosomes, Human, Pair 1, pubmed-meshheading:11425451-Chromosomes, Human, Pair 19, pubmed-meshheading:11425451-Diagnosis, Differential, pubmed-meshheading:11425451-European Continental Ancestry Group, pubmed-meshheading:11425451-Finland, pubmed-meshheading:11425451-Foot, pubmed-meshheading:11425451-Humans, pubmed-meshheading:11425451-In Situ Hybridization, Fluorescence, pubmed-meshheading:11425451-Karyotyping, pubmed-meshheading:11425451-Male, pubmed-meshheading:11425451-Mesenchymoma, pubmed-meshheading:11425451-Middle Aged, pubmed-meshheading:11425451-Neoplasm Metastasis, pubmed-meshheading:11425451-Rhabdomyosarcoma, pubmed-meshheading:11425451-Sarcoma, pubmed-meshheading:11425451-Sweden, pubmed-meshheading:11425451-Translocation, Genetic
pubmed:year
2001
pubmed:articleTitle
A highly aggressive primitive mesenchymal tumor with a translocation (1;19)(q12;q13.2).
pubmed:affiliation
Department of Molecular Medicine, Endocrine Tumor Unit, Karolinska Hospital, SE-171 76 Stockholm, Sweden.
pubmed:publicationType
Journal Article, Case Reports, Research Support, Non-U.S. Gov't