Evidence map›Paper›PMID 39304877›Full record

ArticleBMC women's health2024

Malignant Perivascular epithelioid cell tumour of the uterus without TFE3 gene rearrangement: a case report.

Mu Xu, Jianhui Fu, Liangzhi Cai

Abstract readCase Reports
In one paragraph

Article in BMC women's health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

1 citing paper in PubMed.

  1. 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

3 authors.

Mu XuDepartment of Gynecology, Fujian Maternity and Child Health Hospital, No. 18 Daoshan Road, Fuzhou, 350001, Fujian, China.
Jianhui FuDepartment of Pathology, Fujian Maternity and Child Health Hospital, Fuzhou, China.
Liangzhi CaiDepartment of Gynecology, Fujian Maternity and Child Health Hospital, No. 18 Daoshan Road, Fuzhou, 350001, Fujian, China. 8878431@qq.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPerivascular epithelioid cell tumours (PEComas) are soft tissue tumours. These neoplasms belong to the family of mesenchymal tumours, which include angiomyolipomas, clear-cell sugar tumours of the lung, and PEComas not otherwise specified (NOS). The probability of a perivascular epithelioid cell tumour (PEComa) occurring in the uterus is low, and the incidence, diagnosis, treatment, and outcomes of such tumours are still unclear. CASE PRESENTATION: A 51-year-old woman presented a 4-year history of natural menopause. An intrauterine mass was detected via ultrasound examination; the mass showed a tendency to increase but caused no symptoms. The levels of tumour markers were within the normal range. Pathological analysis of the curettage revealed perivascular epithelioid differentiation of the endometrial tumour. Consequently, a laparoscopic total hysterectomy with bilateral adnexectomy was performed. No distant metastasis was detected via whole-body positron emission computed tomography (PETCT) after the operation. Fluorescence in situ hybridization (FISH) revealed no TFE3 gene rearrangement. Next-generation sequencing of bone and soft tissue revealed negative TSC1/2 and TP53 expression. No recurrence or metastasis was observed during the 18-month follow-up period.

conclusionPEComa of the gynecologic tract is a rare and challenging entity. Diffuse HMB-45 expression, TSC alterations and TFE3 rearrangement are characteristic of uterine PEComas. Surgical resection is the first choice. Genetic testing is helpful for determining the nature of the mass and for choosing targeted therapy. Further research is needed to establish treatment protocols.

Indexed as

Basic Helix-Loop-Helix Leucine Zipper Transcription FactorsGene RearrangementPerivascular Epithelioid Cell NeoplasmsUterine NeoplasmsFemaleHumansHysterectomyMiddle AgedBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsTFE3 protein, humanCase reportPEComaRearrangementTFE3Uterus

Identifiers

PMID39304877
PMCPMC11414286

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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.