Evidence map›Paper›PMID 8579124›Full record

ArticleThe American journal of pathology1996

Correlation between clinicopathological features and karyotype in lipomatous tumors. A report of 178 cases from the Chromosomes and Morphology (CHAMP) Collaborative Study Group.

C D Fletcher, M Akerman, P Dal Cin, I de Wever, N Mandahl, F Mertens, F Mitelman, J Rosai, A Rydholm, R Sciot and 5 more

Abstract read
In one paragraph

Article in The American journal of pathology, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 1 pooled it
22.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

60 citing papers in PubMed, 1 synthesis or guideline pooled it, 335 citations in OpenAlex.

  1. Gene translocations in musculoskeletal neoplasms.Clinical orthopaedics and related research · 2008
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. The Recent Advances in Molecular Diagnosis of Soft Tissue Tumors.International journal of molecular sciences · 2023
    Review
  10. Molecular testing of soft tissue tumors.Diagnostic cytopathology · 2023
    Review
  11. Article
  12. Review
  13. Article
  14. Nuclear expression of MDM2 in hibernoma: a potential diagnostic pitfall.Virchows Archiv : an international journal of pathology · 2021
    Article
  15. A Case of Retroperitoneal Liposarcoma Mimicking an Adrenocortical Carcinoma.Journal of the ASEAN Federation of Endocrine Societies · 2019
    Article
  16. Article
  17. Current management of lipoblastoma.European journal of pediatrics · 2018
    Article
  18. Liposarcoma: Multimodality Management and Future Targeted Therapies.Surgical oncology clinics of North America · 2016
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 1 institution in 1 country.

C D FletcherSt. Thomas's Hospital, London, United Kingdom.
M Akerman
P Dal Cin
I de Wever
N Mandahl
F Mertens
F Mitelman
J Rosai
A Rydholm
R Sciot
G Tallini
H van den Berghe
W van de Ven
R Vanni
H Willen
St Thomas' Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Soft tissue tumors commonly show cytogenetic abnormalities, some of which are tumor specific. Lipomatous tumors represent the largest category of soft tissue neoplasms, and numerous karyotypic aberrations have been identified. However, clear-cut correlation between morphology and karyotype has not been undertaken on a systematic basis in a double-blind setting. The morphological features and histological diagnosis of 178 lipomatous neoplasms were reviewed independently without knowledge of the clinical data. The consensus diagnoses were then correlated with the clinical findings and compared with the tumors' karyotypes, using G-banded preparations from short-term cultures. The data were collated by a multicenter collaborative group of pathologists, geneticists, and surgeons. Clonal chromosomal abnormalities were identified in 149 cases studied (84%) and, to a large extent, the karyotype correlated with the morphological diagnosis. Specifically, 26 (96%) of 27 myxoid liposarcomas and its poorly differentiated variants showed a t(12;16); 29 (78%) of 37 atypical lipomatous tumors (including 5 dedifferentiated cases) showed ring chromosomes; 74 (80%) of 93 subcutaneous and intramuscular lipomas had karyotypic aberrations affecting mainly 12q, 6p, and 13q; 7 of 8 spindle cell and pleomorphic lipomas had aberrations of 16q; 3 lipoblastomas showed 8q rearrangements; and 2 hibernomas showed 11q abnormalities. We conclude that cytogenetic abnormalities are common in lipomatous tumors, correlate reliably with morphological sub-type in many cases, and can be of diagnostic value in histologically borderline or difficult cases.

Indexed as

AdolescentAdultAgedAged, 80 and overAngiolipomaChildChild, PreschoolChromosome AberrationsFemaleHumansKaryotypingLipomaMaleMiddle AgedRetrospective StudiesSoft Tissue Neoplasms

Identifiers

PMID8579124
PMCPMC1861666
OpenAlexW1644457390

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.