Literature DB >> 9109942

Cytogenetic studies in malignant fibrous histiocytoma.

T A Walter1, H J Weh, P M Schlag, C Zornig, D K Hossfeld.   

Abstract

Among soft tissue sarcomas, malignant fibrous histiocytoma is considered to be the most commonly encountered tumor-type of late adult life. Cytogenetic data are, however, sparse and contradictory, without any specific anomalies. We are describing the results of cytogenetic studies in 20 malignant fibrous histiocytomas of various subtypes and gradings. Although we saw two single and therefore possibly primary rearrangements, t(13;14) and t(5;7), most tumors had complex rearrangements without sharing any characteristic aberrations. In our opinion, the heterogeneity of these findings supports the concept that malignant fibrous histiocytoma is not a distinctive entity but merely a name for a group of as yet poorly defined sarcomas.

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Year:  1997        PMID: 9109942     DOI: 10.1016/s0165-4608(96)00220-8

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  3 in total

1.  Diaphyseal medullary stenosis with malignant fibrous histiocytoma: a hereditary bone dysplasia/cancer syndrome maps to 9p21-22.

Authors:  J A Martignetti; R J Desnick; E Aliprandis; K I Norton; P Hardcastle; S Nade; B D Gelb
Journal:  Am J Hum Genet       Date:  1999-03       Impact factor: 11.025

2.  Reclassification and subtyping of so-called malignant fibrous histiocytoma of bone: comparison with cytogenetic features.

Authors:  Fredrik Mertens; Salvatore Romeo; Judith Vmg Bovée; Roberto Tirabosco; Nick Athanasou; Marco Alberghini; Pancras Cw Hogendoorn; Angelo P Dei Tos; Raf Sciot; Henryk A Domanski; Kristina Aström; Nils Mandahl; Maria Debiec-Rychter
Journal:  Clin Sarcoma Res       Date:  2011-10-13

3.  Myxoid malignant fibrous histiocytoma with multiple primary sites.

Authors:  Jeffrey H Muler; Augusto F Paulino; Diane Roulston; Laurence H Baker
Journal:  Sarcoma       Date:  2002
  3 in total

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