Evidence map›Paper›PMID 40880722›Full record

ArticleMaedica2025

Prognostic Significance of Mast Cell Count and Angiogenesis in Central Giant Cell Granulomas of the Jaws.

Marzieh Parto, Monireh Halimi, Shokoufeh Shahrabi-Farahani, Maedeh Vakili Saatloo, Maryam Kouhsoltani

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Article in Maedica, 2025. 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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1 · What the graph read from it

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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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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Marzieh PartoDepartment of Pediatrics, Faculty of Dentistry, Tabriz University of Medical Sciences, Tabriz, Iran.
Monireh HalimiDepartment of Pathology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Shokoufeh Shahrabi-FarahaniDepartment of Diagnostic Sciences, University of Tennessee Health Science Center, College of Dentistry, 875 Union Avenue, Memphis, TN 38103, USA.
Maedeh Vakili SaatlooDepartment of Periodontology, Henry M. Goldman School of Dental Medicine, Boston University, MA, USA.
Maryam KouhsoltaniDepartment of Oral and Maxillofacial Pathology, Faculty of Dentistry, Tabriz University of Medical Sciences, Tabriz, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Mast cells (MCs) secrete different angiogenic factors stimulating angiogenesis. The purpose of this study was to assess MC count and microvessel density (MVD) in aggressive and non-aggressive central giant cell granulomas (CGCGs) of the jaws. Materials and methods: Sixteen aggressive and 14 non-aggressive paraffin-embedded samples of CGCGs were prepared for immunohistochemical analysis using anti-MC tryptase and anti-CD31 antibodies. Results: Mean values±SEM (standard error of mean) for MC count and MVD in aggressive and non-aggressive CGCGs were: 7.48±0.84, 3.85±0.51, 5.55±0.89, 3.19±0.61, respectively. All CGCG cases demonstrated MCs. Differences for both MC count and MVD were statistically significant between aggressive and non-aggressive CGCGs (p=0.002 and p=0.045, respectively), i.e. , MC count and MVD were significantly higher in aggressive lesions. Moreover, there was a significant positive correlation between MC count and MVD in CGCG (r=0.570, p=0.001). Conclusion: Mast cell count and MVD might be used as prognostic markers of aggressive behavior of CGCGs at the time of initial biopsy. Our findings might postulate that therapeutic strategies against MC mediators and angiogenesis may benefit in aggressive CGCG as a non-surgical modality of treatment. With further studies, their prognostic significance and therapeutic application can be evaluated in patients suffering from aggressive CGCG.

Identifiers

PMID40880722
PMCPMC12347035

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