Evidence map›Paper›PMID 37109749›Full record

ArticleMedicina (Kaunas, Lithuania)2023

Inflammatory Myofibroblastic Tumour of the Urinary Bladder in a Middle-Aged Man-A Case Report of an Unusual Localization of a Rare Tumour.

Nebojsa Prijovic, Veljko Santric, Uros Babic, Branko Stankovic, Miodrag Acimovic, Milica Cekerevac, Gorana Nikolic, Bojan Cegar

Open access · goldAbstract readCase Reports
In one paragraph

Article in Medicina (Kaunas, Lithuania), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact, top 89% 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

3 citing papers in PubMed, 0 citations in OpenAlex.

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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 2 institutions in 1 country.

Nebojsa PrijovicClinic of Urology, University Clinical Center of Serbia, 11000 Belgrade, Serbia.ORCID 0000-0002-5268-5801
Veljko SantricClinic of Urology, University Clinical Center of Serbia, 11000 Belgrade, Serbia.
Uros BabicClinic of Urology, University Clinical Center of Serbia, 11000 Belgrade, Serbia.ORCID 0000-0002-0673-9207
Branko StankovicClinic of Urology, University Clinical Center of Serbia, 11000 Belgrade, Serbia.
Miodrag AcimovicClinic of Urology, University Clinical Center of Serbia, 11000 Belgrade, Serbia.
Milica CekerevacDepartment of Pathology, University Clinical Centre of Serbia, 11000 Belgrade, Serbia.
Gorana NikolicFaculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.
Bojan CegarClinic of Urology, University Clinical Center of Serbia, 11000 Belgrade, Serbia.ORCID 0009-0000-1095-8464
University of Belgrade · RSUniverzitetski Klinički Centar Srbije · RS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammatory myofibroblastic tumour (IMT) is a rare tumour with an intermediate biological behaviour. It usually occurs in children and adolescents, primarily in the abdomen or lungs. Histopathologically, IMT consists of spindle cells, i.e., myofibroblasts, and a variable inflammatory component. Localization in the urinary bladder is rare. We are presenting a rare case of IMT in the bladder in a middle-aged man treated by partial cystectomy. A 62-year-old man consulted a urologist because of haematuria and dysuric disturbances. A tumorous mass was detected by an ultrasound in the urinary bladder. CT urography described the tumorous mass at the dome of the urinary bladder measuring 2 × 5 cm. A smooth tumorous mass was cystoscopically observed at the dome of the urinary bladder. Transurethral resection of the bladder tumour was performed. Histopathological analysis of the specimen identified spindle cells with a mixed inflammatory infiltrate; immunohistochemical findings showed positivity for anaplastic lymphoma kinase (ALK), smooth muscle actin (SMA) and vimentin. A histopathological diagnosis of IMT was established. It was decided that the patient would undergo a partial cystectomy. A complete excision of the tumour from the dome of the urinary bladder with surrounding healthy tissue was performed. Histopathological and immunohistochemical findings of the sample confirmed the diagnosis of IMT, without the presence of the tumour at the surgical margins. The postoperative course went smoothly. IMT is a rare tumour in adults, especially localised in the urinary bladder. IMT of the urinary bladder is difficult to distinguish from urinary bladder malignancy both clinically and radiologically, as well as histopathologically. If the location and size of the tumour allow it, bladder-preserving surgeries such as partial cystectomy represent a reasonable modality of operative treatment.

Indexed as

Urinary BladderUrinary Bladder NeoplasmsAdolescentAdultBiomarkers, TumorChildHumansMaleMiddle AgedMyofibroblastsPelvisBiomarkers, Tumorinflammatory myofibroblastic tumourpartial cystectomyurinary bladder

Identifiers

PMID37109749
PMCPMC10144372
OpenAlexW4366414654

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Registered trials

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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.