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dc.creatorDražić, Radojica
dc.creatorSopta, Jelena
dc.creatorMinić, Arsa J.
dc.date.accessioned2020-07-02T12:26:11Z
dc.date.available2020-07-02T12:26:11Z
dc.date.issued2010
dc.identifier.issn0904-2512
dc.identifier.urihttps://smile.stomf.bg.ac.rs/handle/123456789/1521
dc.description.abstractObjective: The aim of this study was to qualitatively and semi-quantitatively analyze mast cells in periapical lesions. Materials and methods: Biopsy specimens of 96 periapical lesions were stained with hematoxylin-eosin, histochemical Giemsa and immunohistochemical CD 117 (C kit) antibody. Mast cell count below 100 mast cells on 1000 fields of high power magnification was noted as 'negative', 101-400 as 'mild', 401-800 cells as 'moderate', and over 800 cells as 'severe'. Results: Mast cells are found in 68 (70.8%) lesions. The presence of mast cells was greater in cysts than in granulomas (P lt 0.0028). There was no difference in semi-quantitative expression of CD 117 in granulomas and cysts (P > 0.05). Mast cells were placed in both: inflammatory infiltrate and in fibroblastic areas of periapical lesions, and their presence was most frequently mild to moderate. Conclusions: The findings of present study could suggest a role of mast cells in regulation of cellular immune mechanisms in periapical lesions, balancing between alterative and reparatory processes in inflamed periapical tissue.en
dc.publisherWiley-Blackwell Publishing, Inc, Malden
dc.rightsrestrictedAccess
dc.sourceJournal of Oral Pathology & Medicine
dc.subjectCD 117en
dc.subjectmast cellsen
dc.subjectperiapical lesionsen
dc.titleMast cells in periapical lesions: potential role in their pathogenesisen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractСопта, Јелена; Минић, Aрса Ј.; Дражић, Радојица;
dc.citation.volume39
dc.citation.issue3
dc.citation.spage257
dc.citation.epage262
dc.citation.other39(3): 257-262
dc.citation.rankM21
dc.identifier.wos000274668700010
dc.identifier.doi10.1111/j.1600-0714.2009.00870.x
dc.identifier.pmid20359310
dc.identifier.scopus2-s2.0-77249172276
dc.type.versionpublishedVersion


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