Literature DB >> 19664493

Sarcomas with spindle cell morphology.

Paola Collini1, Poul H B Sorensen, Shreyaskumar Patel, Jean-Yves Blay, Rolf D Issels, Robert G Maki, Mikael Eriksson, Xavier Garcia del Muro.   

Abstract

In the days before the term "high-grade undifferentiated pleomorphic sarcoma" came into use, one of the most common sarcoma diagnoses was "malignant fibrous histiocytoma," and before that, in an era before immunohistochemistry, "fibrosarcoma" was used to describe most sarcomas. "Spindle cell" is a descriptive phrase that denotes the cellular shape of many of the sarcomas encountered in the adult population. As a result, they are usually treated differently from small round cell sarcomas, and have different biological characteristics than those tumors and sarcomas with epithelioid morphology. As a very broad generalization, sarcomas with a spindle cell microscopic morphology occur in adults and are treated primarily with surgery and often adjuvant or neoadjuvant radiation as primary therapy. In comparison to small round cell sarcomas such as Ewing sarcoma, the use of adjuvant chemotherapy remains controversial, and the sensitivity of these tumors to chemotherapy in the metastatic setting is highly variable. In this article, we describe some of the clinical and biological characteristics of this group of sarcomas.

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Year:  2009        PMID: 19664493     DOI: 10.1053/j.seminoncol.2009.06.007

Source DB:  PubMed          Journal:  Semin Oncol        ISSN: 0093-7754            Impact factor:   4.929


  8 in total

1.  Local mesenchymal stem/progenitor cells are a preferential target for initiation of adult soft tissue sarcomas associated with p53 and Rb deficiency.

Authors:  Jinhyang Choi; Stephen J Curtis; David M Roy; Andrea Flesken-Nikitin; Alexander Yu Nikitin
Journal:  Am J Pathol       Date:  2010-09-23       Impact factor: 4.307

2.  Rapidly recurring ovarian fibrosarcoma after optimal debulking surgery in a 46-year-old woman.

Authors:  Hariyono Winarto; Tantri Hellyanti; Sigit Purbadi; Sutrisno Sutrisno
Journal:  BMJ Case Rep       Date:  2020-07-09

3.  A Trp53fl/flPtenfl/fl mouse model of undifferentiated pleomorphic sarcoma mediated by adeno-Cre injection and in vivo bioluminescence imaging.

Authors:  Marisa R Buchakjian; Nicole M Merritt; Devon L Moose; Adam J Dupuy; Munir R Tanas; Michael D Henry
Journal:  PLoS One       Date:  2017-08-25       Impact factor: 3.240

4.  Spindle cell sarcoma: a SEER population-based analysis.

Authors:  Lei Feng; Meng Wang; Feiluore Yibulayin; Hao Zhang; Yin-Long Yang; Fei Ren; Alimujiang Wushou
Journal:  Sci Rep       Date:  2018-03-22       Impact factor: 4.379

5.  Identification of SETD2-NF1 fusion gene in a pediatric spindle cell tumor with the chromosomal translocation t(3;17)(p21;q12).

Authors:  Ioannis Panagopoulos; Ludmila Gorunova; Ingvild Lobmaier; Bodil Bjerkehagen; Sverre Heim
Journal:  Oncol Rep       Date:  2017-05-04       Impact factor: 3.906

6.  Clear Cell Sarcoma: A Case Report and Review of Literature.

Authors:  Alireza Abdollahi; Fatemeh Khatami; Seyed Mohammad Tavangar
Journal:  Int J Hematol Oncol Stem Cell Res       Date:  2018-01-01

7.  The paradox-breaking panRAF plus SRC family kinase inhibitor, CCT3833, is effective in mutant KRAS-driven cancers.

Authors:  G Saturno; F Lopes; I Niculescu-Duvaz; D Niculescu-Duvaz; A Zambon; L Davies; L Johnson; N Preece; R Lee; A Viros; D Holovanchuk; M Pedersen; R McLeary; P Lorigan; N Dhomen; C Fisher; U Banerji; E Dean; M G Krebs; M Gore; J Larkin; R Marais; C Springer
Journal:  Ann Oncol       Date:  2020-10-29       Impact factor: 32.976

8.  Several fusion genes identified by whole transcriptome sequencing in a spindle cell sarcoma with rearrangements of chromosome arm 12q and MDM2 amplification.

Authors:  Ioannis Panagopoulos; Bodil Bjerkehagen; Ludmila Gorunova; Jeanne-Marie Berner; Kjetil Boye; Sverre Heim
Journal:  Int J Oncol       Date:  2014-08-18       Impact factor: 5.650

  8 in total

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