Evidence map›Paper›PMID 32959210›Full record

ArticleHead and neck pathology2021

Osteosarcoma of the Mandible in a Patient with Florid Cemento-Osseous Dysplasia and Li-Fraumeni Syndrome: A Rare Coincidence.

Simon Haefliger, Dorothee Harder, Michal Kovac, Karin Linkeschova, Harald Eufinger, Daniel Baumhoer

Open access · hybridAbstract readCase Reports
In one paragraph

Article in Head and neck pathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Molecular Alterations in Osteosarcomas of the Oral and Maxillofacial Region: A Scoping Review.Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology · 2026
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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

6 authors at 2 institutions in 2 countries.

Simon HaefligerBone Tumor Reference Center, Institute of Medical Genetics and Pathology, University Hospital of Basel, University of Basel, Schönbeinstrasse 40, 4031, Basel, Switzerland.ORCID http://orcid.org/0000-0002-4227-6051
Dorothee HarderDepartment of Radiology, University Hospital Basel, University of Basel, Basel, Switzerland.
Michal KovacBone Tumor Reference Center, Institute of Medical Genetics and Pathology, University Hospital of Basel, University of Basel, Schönbeinstrasse 40, 4031, Basel, Switzerland.
Karin LinkeschovaDepartment of Oral and Maxillofacial Plastic Surgery, Knappschaftskrankenhaus Recklinghausen, Klinikum Vest, Recklinghausen, Germany.
Harald EufingerDepartment of Oral and Maxillofacial Plastic Surgery, Knappschaftskrankenhaus Recklinghausen, Klinikum Vest, Recklinghausen, Germany.
Daniel BaumhoerBone Tumor Reference Center, Institute of Medical Genetics and Pathology, University Hospital of Basel, University of Basel, Schönbeinstrasse 40, 4031, Basel, Switzerland. daniel.baumhoer@usb.ch.
University of Basel · CHKlinikum Vest · DE

Funding

1 Swiss National Science Foundation2 the foundation of the Basel Bone Tumour Reference Centre3 the Gertrude von Meissner Stiftung4 the Stiftung für krebskranke Kinder, Regio Basiliensis.
6 · The paper itself

Abstract

Cemento-osseous dysplasia (COD) is the most common benign fibro-osseous lesion of the jaws and generally considered non-neoplastic and self-limited. Here, we present a 30-year old female who noticed a bilateral swelling of her posterior mandible with irregular periapical mineralization and incomplete root resorption on panoramic radiographs. A biopsy revealed florid COD and no further treatment was initiated. 9 years later, she presented with a progressive expansion of her left posterior mandible after being treated for bilateral breast cancer 4 and 8 years before. CT scans showed expansile and densely mineralized lesions in all four quadrants with the left posterior mandible showing a focal penetration of the buccal cortical bone. Biopsies revealed an osteoblastic high-grade osteosarcoma in the left and a COD in the right mandible, notably with cellular atypia in the spindle cell component. The patient underwent segmental resection of the left mandible with clear margins and adjuvant chemotherapy. Subsequent genetic testing identified a heterozygous germline TP53 mutation (p.V173G) which confirmed the clinically suspected Li-Fraumeni syndrome (LFS). 3 years after the resection, the patient is free of disease and the other foci of COD remained stable in size on follow-up imaging analyses. Our case illustrates LFS-related osteosarcoma developing within florid COD. Given the rarity of this coincidence, a causative relation between the two lesions seems unlikely but in patients with tumor predisposition syndromes it might be advisable to closely monitor even benign lesions like COD.

Indexed as

AdultFemaleFibrous Dysplasia of BoneHumansLi-Fraumeni SyndromeMandibular NeoplasmsOsteomyelitisOsteosarcomaCemento-osseous dysplasiaLi–Fraumeni syndromeOsteosarcoma of the mandible

Identifiers

PMID32959210
PMCPMC8134641
OpenAlexW3087032073

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.