Evidence map›Paper›PMID 37799476›Full record

ArticleFrontiers in oncology2023

Malignant lung PEComa (clear cell tumor): rare case report and literature review.

Marcos Adriano Garcia Campos, Lucas Fernandes Vasques, Rafael Goulart de Medeiros, Érico Murilo Monteiro Cutrim, Ana Júlia Favarin, Sarah Rebecca Machado Silva, Gyl Eanes Barros Silva, Marcelo Padovani de Toledo Moraes, Mariana Lopes Zanatta, Diego Aparecido Rios Queiróz

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In one paragraph

Article in Frontiers in oncology, 2023. 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
0.9field-weighted citation impact, top 26% 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, 5 citations in OpenAlex.

  1. Review
  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

10 authors at 3 institutions in 1 country.

Marcos Adriano Garcia CamposDepartment of Internal Medicine, Hospital of Medical School of São Paulo State University, Botucatu, Brazil.
Lucas Fernandes VasquesDepartment of Medicine, University of Taubate Faculty of Medicine, Taubaté, Brazil.
Rafael Goulart de MedeirosDepartment of Medicine, University of Taubate Faculty of Medicine, Taubaté, Brazil.
Érico Murilo Monteiro CutrimDepartment of Internal Medicine, Hospital of Medical School of São Paulo State University, Botucatu, Brazil.
Ana Júlia FavarinDepartment of Internal Medicine, Hospital of Medical School of São Paulo State University, Botucatu, Brazil.
Sarah Rebecca Machado SilvaDepartment of Internal Medicine, Hospital of Medical School of São Paulo State University, Botucatu, Brazil.
Gyl Eanes Barros SilvaLaboratory of Immunofluorescence and Electron Microscopy, University Hospital of Federal University of Maranhão, São Luís, Brazil.
Marcelo Padovani de Toledo MoraesDepartment of Internal Medicine, Hospital of Medical School of São Paulo State University, Botucatu, Brazil.
Mariana Lopes ZanattaDepartment of Internal Medicine, Hospital of Medical School of São Paulo State University, Botucatu, Brazil.
Diego Aparecido Rios QueirózDepartment of Internal Medicine, Hospital of Medical School of São Paulo State University, Botucatu, Brazil.
Universidade Estadual Paulista (Unesp) · BRUniversidade de Taubaté · BRUniversidade Federal do Maranhão · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clear cell tumors of the lung (CCTL), or "sugar tumors" of lung, are very uncommon lesions and are mostly benign perivascular epithelioid cell (PEC) tumors with no specific morphologic features. Fewer than 100 cases have been reported; the aggressive nature demonstrated in sporadic reports has rarely been described in the literature. Although the course is generally described as benign, eight reported cases showed malignant behavior. We report a case of a PEC with a malignant presentation in a young man, correlating the main characteristics of the tumor with other cases reported in the literature to better elucidate this rare presentation. We also performed a literature review of reports on benign and malignant CCTL cases, with a focus on clinical, imaging, and immunohistochemical differentiation. CCTLs are rare tumors that require histopathological and immunohistochemical confirmation; to date, criteria that can predict malignant evolution are lacking.

Indexed as

cathepsin KHMB-45PEComapulmonary cancersugar tumor

Identifiers

PMID37799476
PMCPMC10547894
OpenAlexW4386931840

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.