15
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Expression of CD34 and CD68 in peripheral giant cell granuloma and central giant cell granuloma: An immunohistochemical analysis

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background:

          Central and Peripheral giant cell granulomas of jaws are uncommon, benign, reactive disorders that are characterized by the presence of numerous multinucleated giant cells and mononuclear cells within a stroma. The origin of the multinucleated giant cells is controversial; probably originating from fusion of histiocytes, endothelial cells and fibroblasts.

          Objective:

          To assess the expression of CD34 and CD68 in central and peripheral giant cell granulomas to understand the origin of these multinucleated giant cells.

          Materials and Methods:

          Twenty cases of Central and Peripheral giant cell granulomas were evaluated immunohistochemically for CD34 and CD68 proteins expression.

          Results:

          Immunopositivity for CD34 was seen only in cytoplasm of endothelial cells of blood vessels; whereas, consistent cytoplasmic immunopositivity for CD68 was seen in few stromal cells. Statistical significance was seen in mean number of multinucleated giant cells, mean number of nuclei in multinucleated giant cells, CD68 expression and ratio of macrophages to multinucleated giant cells among two lesions.

          Conclusion:

          Although the central giant cell granulomas share some clinical and histopathological similarities with peripheral giant cell granulomas, differences in mean number of nuclei in multinucleated giant cells and CD68 immunoreactivity may underlie the distinct clinical behavior.

          Related collections

          Most cited references28

          • Record: found
          • Abstract: found
          • Article: not found

          Giant cell formation and function.

          To provide insight into the current state of understanding regarding the molecular and cellular mechanisms underlying the formation and function of various types of multinucleated giant cells. Recent studies involving mainly osteoclasts and foreign body giant cells have revealed a number of common factors, for example, vitronectin, an adhesion protein, dendritic cell-specific transmembrane protein, a fusion factor, and macrophage fusion receptor, that contribute to giant cell formation and function. Insight into common molecules, receptors, and mediators of adhesion and fusion mechanisms of giant cell formation have been complicated by the wide diversity of species, models, and cell types utilized in these studies. These recently identified factors together with the well known osteoclast receptor, alphavbeta3, may serve as potential therapeutic targets for the modulation and inhibition of multinucleated giant cell formation and function. Further studies on intracellular and intercellular signaling mechanisms modulating multinucleated giant cell formation and function are necessary for the identification of therapeutic targets as well as a better understanding of giant cell biology.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Tartrate-resistant acid phosphatase 5b (TRACP 5b) as a marker of bone resorption.

            Tartrate-resistant acid phosphatase (TRACP) is an enzyme that is expressed in high amounts by bone resorbing osteoclasts, inflammatory macrophages and dendritic cells. Two forms of TRACP circulate in human blood, TRACP 5a derived from macrophages and dendritic cells, and TRACP 5b derived from osteoclasts. Recent data have demonstrated the utility of TRACP 5b as a marker of osteoclast number and bone resorption, and serum TRACP 5a as a marker of inflammatory conditions. This review summarizes the scientific knowledge on the role of TRACP in osteoclastic bone resorption, the mechanism of TRACP 5b generation in osteoclasts and its secretion into the blood circulation, the methodology of measuring TRACP 5b, diagnostic evidence for the use of TRACP 5b as a resorption marker, and characteristics of TRACP 5b compared to other commonly used bone turnover markers.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Diagnostic Surgical Pathology of the Head and Neck

              DR Gnepp (2001)
                Bookmark

                Author and article information

                Journal
                J Oral Maxillofac Pathol
                J Oral Maxillofac Pathol
                JOMFP
                Journal of Oral and Maxillofacial Pathology : JOMFP
                Medknow Publications & Media Pvt Ltd (India )
                0973-029X
                1998-393X
                Sep-Dec 2014
                : 18
                : 3
                : 341-348
                Affiliations
                [1] Department of Oral Pathology, Rajarajeswari Dental College and Hospital, Mysore, Bangalore, India
                [1 ] Department of Oral Pathology, Sri Dharmasthala Manjunatheshwara Dental College, Dharwad, Karnataka, India
                Author notes
                Address for correspondence: Dr. Sanjay Murgod, Department of Oral Pathology, RRDC, No. 14, Ramohally Cross, Kumbalgodu, Mysore Road, Mysore, Bangalore 560 060, Karnataka, India. E-mail: smurgod@ 123456yahoo.com
                Article
                JOMFP-18-341
                10.4103/0973-029X.151310
                4409176
                25948986
                d6ef2f77-3e36-4ceb-a174-d4cf68193e0a
                Copyright: © Journal of Oral and Maxillofacial Pathology

                This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 01 August 2013
                : 31 December 2014
                Categories
                Original Article

                Pathology
                cd34,cd68,central and peripheral giant cell granulomas
                Pathology
                cd34, cd68, central and peripheral giant cell granulomas

                Comments

                Comment on this article