Evidence map›Paper›PMID 40515886›Full record

ArticleInsights into imaging2025

Diagnostic work-up of lipomatous tumors: a decision-making analysis among European sarcoma centers.

Ali Naimi, Paul Martin Putora, Christian Rothermundt, Antonia Digklia, Jose Manuel Asencio, Sylvie Bonvalot, Florian Bösch, Anant Desai, Amer James Durrani, Haim Gutman and 12 more

Abstract read
In one paragraph

Article in Insights into imaging, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. [A case report of recurrent giant intermuscular lipoma in the temporal region].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2026
    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

22 authors.

Ali NaimiRadiology and Nuclear Medicine, Kantonsspital St. Gallen, St. Gallen, Switzerland. alinaimi2@gmail.com.ORCID http://orcid.org/0009-0000-3147-475X
Paul Martin PutoraDepartment of Radiation Oncology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Christian RothermundtDivision of Medical Oncology and Hematology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Antonia DigkliaSarcoma Center, Centre Hospitalier Universitaire Vaudois, University of Lausanne, Lausanne, Switzerland.
Jose Manuel AsencioGeneral Surgery III Department and Liver Transplant Unit, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Sylvie BonvalotDepartment of Surgical Oncology, Institut Curie, Paris, France.
Florian BöschDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, Göttingen, Germany.
Anant DesaiMidlands Abdominal and Retroperitoneal Sarcoma Unit (MARSU), University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom.
Amer James DurraniDepartment of Plastic Surgery, University of Cambridge and Addenbrooke's Hospital, Cambridge, UK.
Haim GutmanSurgical Oncology Unit, Department of Surgery, Herzliya Medical Center, Herzliya, Israel.
Daphne HompesDepartment of Surgical Oncology, University Hospitals Gasthuisberg, Leuven, Belgium.
Jens JakobSarcoma Unit, Department of Surgery, University Medical Center and Medical Faculty Mannheim, University of Heidelberg, Mannheim, Germany.
Wolfram Trudo KnoefelDepartment of General, Visceral and Pediatric Surgery, University Hospital, Medical Faculty, Heinrich-Heine-University Duesseldorf, Duesseldorf, Germany.
Elisabetta PennacchioliDivision of Melanoma, Sarcomas and Rare Tumors, IEO, European Institute of Oncology, IRCCS, Milan, Italy.
Piotr RutkowskiDepartment of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Winan J van HoudtThe Division of Surgical Oncology, Netherlands Cancer Institute, Department of Medical Oncology, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Barbara L van LeeuwenDepartment of Surgery, University Medical Center Groningen, Groningen, The Netherlands.
Stephan WaeltiRadiology and Nuclear Medicine, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Tim Steffen FischerFaculty of Medicine, University of Zurich, Zurich, Switzerland.
Stefan MarkartRadiology and Nuclear Medicine, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Simon WildermuthRadiology and Nuclear Medicine, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Tobias Johannes DietrichRadiology and Nuclear Medicine, Kantonsspital St. Gallen, St. Gallen, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesLipomatous soft-tissue tumors present a diagnostic burden. The aim of this work was to compare standard operating procedures (SOPs) for the diagnostic management of lipomatous soft-tissue tumors among European academic centers.

methodsExperts of the Soft Tissue and Bone Sarcoma Group of the European Organization for Research and Treatment of Cancer were asked for their SOPs in the diagnosis of adipocytic soft-tissue tumors in an otherwise healthy patient. The answers were converted to decision trees and subsequently compared using the objective consensus methodology. Mediastinal and retroperitoneal lipomatous tumors were excluded from the analysis.

resultsThe highest consensus (93%) among fourteen institutions was noted for evaluation with core needle biopsy (CNB) as SOP for lipomatous tumors located deep in tissue exceeding 7 cm and tumor-associated symptoms. Evaluation of heterogeneous features on imaging by CNB usually showed a consensus rate of at least 75%. Consensus was less likely for lipomatous tumors without symptoms or heterogeneous features. In these settings, CNB and follow-up were almost equally recommended. For lipomatous tumors smaller than 3 cm, without growth or symptoms, no localization in the trunk, and homogeneous imaging features, a consensus rate of 71% was achieved for follow-up.

conclusionsSOPs for diagnostic work-up of lipomatous tumors varied despite their geographical proximity. The highest consensus for biopsy was for deep large tumors with associated symptoms. For follow-up, consensus was shown for small homogenous tumors outside the trunk, without growth or symptoms. Consensus on resection involved homogeneous deeply located small tumors outside the trunk with growth and symptoms. CRITICAL RELEVANCE STATEMENT: This study identifies the decision-making criteria with the highest consensus rate among participating academic sarcoma centers in diagnosing lipomatous tumors: tumors located deep in the tissue, a tumor size exceeding 7 cm, and associated symptoms emerge as pivotal criteria. KEY POINTS: Standard operating procedures for diagnostic work-up of lipomatous tumors among fourteen sarcoma centers were analyzed. Identified diagnostic criteria are: imaging features, size, growth, symptoms, superficial and trunk location. The highest consensus concerned recommending biopsies for deep tumors > 7 cm with associated symptoms.

Indexed as

Adipocytic soft-tissue tumorDecision-makingDiagnostic managementLipomaLiposarcoma

Identifiers

PMID40515886
PMCPMC12167213

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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.