Evidence map›Paper›PMID 32334443›Full record

ArticleJournal of surgical oncology2020

Adamantinomatous tumors: Long-term follow-up study of 20 patients treated at a single institution.

Eugenia Schwarzkopf, Yoely Tavarez, John H Healey, Meera Hameed, Daniel E Prince

Abstract readCase Reports
In one paragraph

Article in Journal of surgical oncology, 2020. 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
–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

5 citing papers in PubMed.

  1. Article
  2. Tibial Adamantinoma: A Case Report from a Resource-Limited-Setting.International medical case reports journal · 2024
    Article
  3. Review
  4. Article
  5. Adamantinoma: An Updated Review.In vivo (Athens, Greece)
    Review
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

5 authors.

Eugenia SchwarzkopfSloan Kettering Institute, New York, New York.ORCID http://orcid.org/0000-0002-0305-5686
Yoely TavarezDepartment of Surgery, Orthopaedic Service, Memorial Sloan-Kettering Cancer Center, New York, New York.
John H HealeyDepartment of Surgery, Orthopaedic Service, Memorial Sloan-Kettering Cancer Center, New York, New York.ORCID http://orcid.org/0000-0002-0802-1186
Meera HameedDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Daniel E PrinceDepartment of Surgery, Orthopaedic Service, Memorial Sloan-Kettering Cancer Center, New York, New York.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Cycle for Survival N/ANational Institutes of Health/National Cancer Institute #P30CA008748NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

BACKGROUND AND

objectivesAdamantinomas are primary, low-grade malignant tumors of the bone that have metastatic potential to the lungs, lymph nodes, and other regions. The rarity of this disease and its nonspecific symptoms complicate diagnosis. MATERIALS AND

methodsRecords for 20 patients who underwent treatment for adamantinoma from 1975 to 2018 were reviewed for demographic, clinical, and pathological data, treatment details, postoperative complications, and outcomes.

resultsPatients presented at a median age of 22 years (1-79 years): 14 patients had a localized primary tumor, three presented with local recurrence, and three with metastatic disease. Median tumor size was 5.7 cm (0.5-15.5 cm). Wide excision was performed primarily in 15 cases; the remaining five patients underwent intralesional curettage. At a median follow-up of 7.3 years, 14 patients had no evidence of disease; two patients were alive with disease, and four patients died from the disease. Local recurrence and distant metastasis occurred at a median of 11.4 years (6 month-19 years) and 15.8 years (4 month-23 years) after diagnosis.

conclusionsAdequate histopathological diagnosis is crucial to avoid misdiagnosis of this rare tumor. Local and distant recuAbs_Para_meprrence can occur more than 20 years after the initial diagnosis. Life-long follow-up with clinical examination and imaging is required.

Indexed as

AdamantinomaAdolescentAdultAgedChildChild, PreschoolCytoreduction Surgical ProceduresFemaleFollow-Up StudiesHumansInfantMaleMiddle AgedNeoplasm MetastasisNeoplasm Recurrence, LocalPostoperative Complicationsadamantinomabone-tumorlow-gradeosteofibrous dysplasia

Identifiers

PMID32334443
PMCPMC7547203

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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.