Evidence map›Paper›PMID 39790741›Full record

ArticleJournal of family medicine and primary care2024

Gastrointestinal stromal tumors mimicking as gynecological tumors-A case series.

Kiran Trivedi, Shabnam Toppo, Apoorwa Sharma, Rohit Kumar Jha, Binit Bharati, Pushpanjali, Tulika Sinha

Abstract readCase Reports
In one paragraph

Article in Journal of family medicine and primary care, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Kiran TrivediDepartment of Obstetrics and Gynecology, Rajendra Institute of Medical Sciences, Ranchi, Jharkhand, India.
Shabnam ToppoDepartment of Obstetrics and Gynecology, Rajendra Institute of Medical Sciences, Ranchi, Jharkhand, India.
Apoorwa SharmaDepartment of Obstetrics and Gynecology, Bharati Vidyapeeth Medical College, Pune, Maharashtra, India.
Rohit Kumar JhaDepartment of Oncosurgery, Rajendra Institute of Medical Sciences, Ranchi, Jharkhand, India.
Binit BharatiDepartment of General Surgery, Rajendra Institute of Medical Sciences, Ranchi, Jharkhand, India.
PushpanjaliDepartment of Pathology and Trauma Central lab, RIMS, Ranchi, Jharkhand, India.
Tulika SinhaDepartment of Obstetrics and Gynecology, Rajendra Institute of Medical Sciences, Ranchi, Jharkhand, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastrointestinal stromal tumors (GISTs) are rare mesenchymal tumors that arise from interstitial cells of Cajal. Due to vague presentation, location and confusing imaging studies, they tend to mimic gynaecological tumors. They usually diagnosed intra-operative and histopathology followed by tumor specific receptors such as KIT, CD34, CD 117 and DOG 1 are mainstay of diagnosis of GIST. Prognosis of GISTs depends on mitotic rate, tumor size and organ of origin. Resection of mass with tumor free margins is the target of treatment. L ymphadenectomy is not routine. Chemotherapy with tyrosine kinase inhibitors such as Imatinib, Dasatinib, Sorafenib and follow- up depend upon risk category. In this case series, there were four cases with vague symptoms misdiagnosed as gynaecological tumors are reviewed. Preoperatively tumors assumed to be of gynaecological origin were found to be case of GISTs intra-operatively and confirmed by presence of cajal's cells histopathology and mainly by DOG 1, CD117 and tyrosine kinase inhibitor receptors on immunohistochemistry. All belonged to high risk category of GISTs. Any abdomino-pelvic mass detected on ultrasonography and with unusual presentation presenting at primary health centre the possibility of non-gynecological tumors especially GISTs should be kept in mind and should be referred to higher centres for further investigation and proper management.

Indexed as

CD 117 and DOG 1Gastrointestinal tumorsgynaecological tumorshistopathologyimmunohistochemistryinterstitial cells of Cajal’styrosine kinase inhibitors

Identifiers

PMID39790741
PMCPMC11709065

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