Evidence map›Paper›PMID 38502367›Full record

ReviewHead and neck pathology2024

Xanthoma of the Jaw Bones: Cases Series and Review of Literature.

Shankar Venkat, Mohammed N Islam, Indraneel Bhattacharyya, Donald M Cohen, F James Kratochvil, Tina R Woods, Seema Ganatra, Saja A Alramadhan

Open access · hybridAbstract readCase ReportsReview
In one paragraph

Review in Head and neck pathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

8 authors at 6 institutions in 2 countries.

Shankar VenkatDepartment of Oral and Maxillofacial Pathology, University of Florida College of Dentistry, Gainesville, FL, USA.
Mohammed N IslamDepartment of Oral and Maxillofacial Pathology, University of Florida College of Dentistry, Gainesville, FL, USA.
Indraneel BhattacharyyaDepartment of Oral and Maxillofacial Pathology, University of Florida College of Dentistry, Gainesville, FL, USA.
Donald M CohenDepartment of Oral and Maxillofacial Pathology, University of Florida College of Dentistry, Gainesville, FL, USA.
F James KratochvilDepartment of Pathology and Radiology, Oregon Health and Science University School of Dentistry, Portland, OR, USA.
Tina R WoodsThe Medical University of South Carolina, Charleston, SC, USA.
Seema GanatraUniversity of Alberta, Edmonton Clinic Health Academy, Edmonton, AB, Canada.
Saja A AlramadhanUniversity of Mississippi Medical Center, 2500 N. State St, Jackson, MS, 39216-4505, USA. salramadhan@umc.edu.
Florida College · USUniversity of Florida · USJackson Memorial Hospital · USMedical University of South Carolina · USOregon Health & Science University · USUniversity of Alberta · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIntraosseous xanthomas are rare benign lesions sometimes associated with excess lipid production. Xanthoma of the jaw bones (XJB) was first reported in 1964, and fewer than 50 cases have been reported in the English literature to date. The etiopathogenesis of XJB is highly suggestive of a reactive process or a metabolic condition.

methodSeven cases of XJBs were retrieved from the archives of 4 oral and maxillofacial pathology services. Clinical, radiographic and histopathologic features of all these cases were retrospectively analyzed. Immunohistochemical (IHC) stains for S100 and CD68 were performed.

resultsAll seven cases involved the mandible. Patients' age ranged between 13 and 69 years with an evenly distributed female to male ratio. One patient had a medical history of hyperlipidemia, but the medical and dental histories of the others were unremarkable. For most cases, XJB was an incidental finding discovered during routine radiographic examination. Swelling and cortical expansion were noted in a few cases. Radiographically, cases typically presented as either well-defined multilocular or unilocular lesions, which were either radiolucent or mixed radiolucent/radiopaque. All the lesions were treated with surgical curettage and no recurrence was observed during subsequent follow-ups. Each of the seven cases exhibited sheets of foamy macrophages. The diagnosis is established by exclusion of entities with overlapping microscopic features and involved correlation with the clinical, histological, radiographic and IHC profiles. Immunohistochemically, all the cases expressed diffuse positivity for CD68 and were negative for S100.

conclusionXJB is a rare lesion of unknown etiology, which may mimic other benign or reactive jaw lesions. Due to its rarity and the potential diagnostic challenges it presents, clinicians must remain vigilant and consider CXJ in their differential when assessing radiolucent jaw anomalies.

Indexed as

Bone DiseasesXanthomatosisAdolescentAdultAgedDiagnosis, DifferentialFemaleHumansMaleMandibleMiddle AgedRetrospective StudiesYoung AdultHyperlipidemiaMultilocularOsseous LesionRadiolucencyXanthoma

Identifiers

PMID38502367
PMCPMC10951172
OpenAlexW4392950003

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.