Literature DB >> 3021318

Flow cytometric analysis of nephroblastomas and related neoplasms.

D Schmidt, B Wiedemann, W Keil, E Sprenger, D Harms.   

Abstract

A total of 59 cases of nephroblastoma and related neoplasms were studied by flow cytometry of paraffin-embedded tissue. According to clinical prognosis, cases were subdivided into three groups: Group 1 (low risk) consisted of congenital mesoblastic nephroma (n = 13) and cystic, partially differentiated nephroblastoma (n = 2). Group 2 (intermediate risk) comprised the various subtypes of "typical" nephroblastoma (n = 24) including cases of fetal rhabdomyomatous nephroblastoma (n = 4). In group 3 (high risk) there were cases of anaplastic nephroblastoma (n = 3), clear cell sarcoma of the kidney or "bone metastasizing renal tumor of childhood" (n = 7), and malignant rhabdoid tumor of the kidney (n = 6). The three clinically different groups of tumors also varied in the proportion of cases with aneuploid tumor DNA stemlines, in S-phase fractions, and in proliferation indices (PI = S + G2 + M). Group 1 was generally characterized by a small number of cases with aneuploid tumor DNA stemlines and low values for S-phase fractions and PI, whereas Group 3 showed the largest number of cases with aneuploid tumor DNA stemlines and high values for S-phase fractions and PI. Group 2 was in between. It is concluded that flow cytometry on paraffin-embedded tissue from pediatric tumors may be a useful adjunct in determining prognosis, and that the subdivision of nephroblastomas and related neoplasms into three prognostically different groups is warranted.

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Year:  1986        PMID: 3021318     DOI: 10.1002/1097-0142(19861201)58:11<2494::aid-cncr2820581124>3.0.co;2-j

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  6 in total

1.  DNA quantitation of Wilms' tumour (nephroblastoma) using flow cytometry and image analysis.

Authors:  S Gururangan; A Dorman; R Ball; B Curran; M Leader; F Breatnach; A O'Meara
Journal:  J Clin Pathol       Date:  1992-06       Impact factor: 3.411

2.  Ploidy changes between diagnosis and relapse in childhood renal tumours.

Authors:  A O'Meara; S Gururangan; R Ball; E Kay; A Kelsey
Journal:  Urol Res       Date:  1993

3.  Chromosome aberrations in mesoblastic nephroma.

Authors:  D E Schofield; E J Yunis; J A Fletcher
Journal:  Am J Pathol       Date:  1993-09       Impact factor: 4.307

4.  Prognostic relevance of DNA content in childhood renal tumours.

Authors:  S Kumar; H B Marsden; R A Cowan; J M Barnes
Journal:  Br J Cancer       Date:  1989-02       Impact factor: 7.640

5.  A non-diploid DNA status is linked to poor prognosis in renal cell cancer.

Authors:  Franziska Büscheck; Christoph Fraune; Martina Kluth; Maximilian Lennartz; Ronald Simon; Claudia Hube-Magg; Christian Morlock; Silvano Barbieri; Carolin Wahl; Christian Eichelberg; Christina Möller-Koop; Doris Höflmayer; Corinna Wittmer; Waldemar Wilczak; Guido Sauter; Margit Fisch; Till Eichenauer; Michael Rink
Journal:  World J Urol       Date:  2020-05-02       Impact factor: 4.226

6.  DNA ploidy and proliferative activity (S-phase) in childhood soft-tissue sarcomas: their value as prognostic indicators.

Authors:  F K Niggli; J E Powell; S E Parkes; K Ward; F Raafat; J R Mann; M C Stevens
Journal:  Br J Cancer       Date:  1994-06       Impact factor: 7.640

  6 in total

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