Evidence map›Paper›PMID 42169394›Full record

SynthesisClinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery2026

Inflammatory Myofibroblastic Tumour of Head and Neck: A Systematic Review Plus Meta-Analysis.

Alireza Sharifi, Mohaddeseh Zojaji, Narges Badragheh, Mehran Jamali, Sahar Ghaedsharaf, Maryam Yaghoubi Hamgini, Mohammad E Ghaffari, Samad Samadizadeh, Hassan H Ramadan, Meghan T Turner

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Alireza SharifiOtorhinolaryngology Research Center, Department of Otolaryngology Head and Neck Surgery, Amir A'lam Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Mohaddeseh ZojajiDigestive Diseases Research Center, Tehran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0002-9775-7100
Narges BadraghehFiroozabadi Clinical Research Development Unit, Department of Radiology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Mehran JamaliDepartment of Oral and Maxillofacial Surgery, School of Dentistry, Qom University of Medical Sciences, Qom, Iran.
Sahar GhaedsharafDepartment of Oral and Maxillofacial Radiology, School of Dentistry, Shahid Beheshti University, Tehran, Iran.
Maryam Yaghoubi HamginiENT and Head and Neck Research Center and Department, the Five Senses Health Institute, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Mohammad E GhaffariDepartment of Epidemiology and Biostatistics, Faculty of Health, Qom University of Medical Sciences, Qom, Iran.ORCID https://orcid.org/0000-0002-8301-8710
Samad SamadizadehDepartment of Oral and Maxillofacial Surgery, School of Dentistry, Isfahan University of Medical Sciences, Isfahan, Iran.
Hassan H RamadanDepartment of Otolaryngology-Head and Neck Surgery, West Virginia University, Morgantown, West Virginia, USA.ORCID https://orcid.org/0000-0002-9077-8291
Meghan T TurnerDepartment of Otolaryngology-Head and Neck Surgery, West Virginia University, Morgantown, West Virginia, USA.ORCID https://orcid.org/0000-0001-8621-6168

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThis systematic review with meta-analysis is aimed to examine clinical presentations, pathologic and imaging findings, treatment approaches, and prognosis of inflammatory myofibroblastic tumour.

methodsPubMed, Medline, Scopus, Cochrane Central Register of Control Trials, Web of Science, Google Scholar, and Embase were systematically searched up to February 2026. The search strategy was structured by a combination of relevant keywords and medical subheadings. This review adhered to Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines and Population, Intervention, Comparison, and Outcome (PICO) statement.

resultsA total of 22 studies, including 337 patients, met the inclusion criteria. Most of the tumours originated from the sinonasal space (40.1%, proportion = 163), and the maxilla bone and hypopharynx had the least frequency (0.3%, proportion = 1). The most prevalent manifestations were proptosis and facial pain/swelling. Regarding immunohistochemical findings, tumours were mostly positive for vimentin and SMA, while they were commonly negative for desmin, S-100, anaplastic lymphoma kinase, and CD34. Many patients were treated with surgical resection alone without any recurrence occurring. Recurrence occurred in 21.6% (proportion = 67). Metastases occurred in 8.8% (proportion = 8).

conclusionsThe diagnosis of head and neck inflammatory myofibroblastic tumour appears related to the presence of vimentin, SMA, desmin, anaplastic lymphoma kinase, CD34, and S-100 on immunohistochemistry. The enhancement pattern on computed tomography cannot help diagnosis, but absence of calcification may distinguish tumour from other differential diagnoses. Surgical resection with a free margin is the most common treatment approach. Metastasis and malignant transformation rarely occur in this tumour of the head and neck region.

Indexed as

Granuloma, Plasma CellHead and Neck NeoplasmsHumansPrognosisheadinflammatory myofibroblastic tumourneckoral and maxillofacialotorhinolaryngology

Identifiers

PMID42169394
PMCPMC13432647

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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.