The American Journal of Surgical Pathology · 2001 · 199 citations · 23 references
Life SciencesOncologyPathologyCancer GeneticsCytogeneticsNeoplasiaCancer CytogeneticsChromosomal AbnormalitiesChromosomal TranslocationsMolecular CytogeneticsNeoplastic TransformationTumor ClassificationChromosomal Translocation AnalysisCytogenetic AberrationsCytogenetic AbnormalitiesEpithelioid HemangioendotheliomaHistopathologic ExaminationKaryotypic AbnormalitiesNeoplastic DiseaseUnbalanced Chromosomal Translocation
The cytogenetic findings for two epithelioid hemangioendotheliomas are reported. An identical chromosomal translocation involving chromosomes 1 and 3 [t(1;3)(p36.3;q25)] was detected in both cases of epithelioid hemangioendothelioma, possibly representing a characteristic rearrangement for this histopathologic entity. The presence of clonal karyotypic abnormalities supports a neoplastic origin for the epithelioid variant of hemangioendothelioma. Identification of the 1;3 translocation may be useful diagnostically. Should additional studies confirm these data, this could lead to the identification of the gene(s) central to this neoplastic process.
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Fusion of PAX7 to FKHR by the variant t(1;13)(p36;q14) translocation in alveolar rhabdomyosarcoma.
Richard J. Davis, Celina M. D’Cruz, Mark A. Lovell et al. · PubMed · 1994 · 599 citations
Life Sciences, Genetics, Oncology +17
Eduardo Calonje, Christopher D.�M. Fletcher, E. WILSON‐JONES et al. · The American Journal of Surgical Pathology · 1994 · 224 citations