Publication: Immunophenotype of Dental Implant-Associated Peripheral Giant Cell Reparative Granuloma in a Representative Case Report.
dc.contributor.author | Galindo-Moreno, Pablo | |
dc.contributor.author | Hernández-Cortés, Pedro | |
dc.contributor.author | Ríos, Rosa | |
dc.contributor.author | Sánchez-Fernández, Elena | |
dc.contributor.author | Cámara, Miguel | |
dc.contributor.author | O'Valle, Francisco | |
dc.date.accessioned | 2023-01-25T08:30:34Z | |
dc.date.available | 2023-01-25T08:30:34Z | |
dc.date.issued | 2013-09-23 | |
dc.description.abstract | We report the case of a 74-year-old white male patient who had worn an overdenture for the previous 6 years, retained by 4 screwed implants and a bar, who presented with an exophytic multilobed lesion of 2.5 × 2.0 cm on the anterior aspect of 1 implant neck, which was surrounded by pink-reddish tissue. All of the soft tissue around the implant was removed until the periosteum was reached. Histologic examination of the lamina propria revealed a cellular proliferation with imprecise boundaries, dense stromal component composed of spindle- to round-shaped mononucleated cells (fibroblasts and monocytes/macrophages), abundant multinucleated giant cells surrounding microscopic hemorrhagic foci, and deposits of hemosiderin; the diagnosis was peripheral giant-cell reparative granuloma (PGCG). Giant cells share the immunohistochemical expression of monocyte/macrophage markers (CD68, calprotectin [Mc387]) and osteoclastic cell markers (tartrate-resistant acid phosphatase, cathepsin K, and microphthalmia-associated transcription factor). After 6 months of follow-up, no bone resorption or recurrence of implant loss was observed. There have been only 12 case reports on dental implant-associated PGCG. Research results to date indicate that there may be little difference in immunophenotype among the giant cells of PGCG, central giant cell reparative granuloma, and peri-implant osteolysis. In conclusion, the immunohistochemical study confirms an osteoclast like giant cells phenotype differentiation in PGCG. | |
dc.identifier.doi | 10.1563/AAID-JOI-D-13-00155 | |
dc.identifier.essn | 1548-1336 | |
dc.identifier.pmid | 24059329 | |
dc.identifier.uri | http://hdl.handle.net/10668/9716 | |
dc.issue.number | 1 | |
dc.journal.title | The Journal of oral implantology | |
dc.journal.titleabbreviation | J Oral Implantol | |
dc.language.iso | en | |
dc.organization | Hospital Universitario San Cecilio | |
dc.page.number | 55-60 | |
dc.pubmedtype | Case Reports | |
dc.pubmedtype | Journal Article | |
dc.subject | dental implant | |
dc.subject | peripheral giant cell reparative granuloma | |
dc.subject.mesh | Aged | |
dc.subject.mesh | Dental Implants | |
dc.subject.mesh | Giant Cells | |
dc.subject.mesh | Granuloma, Giant Cell | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Male | |
dc.subject.mesh | Osteoclasts | |
dc.subject.mesh | Osteolysis | |
dc.title | Immunophenotype of Dental Implant-Associated Peripheral Giant Cell Reparative Granuloma in a Representative Case Report. | |
dc.type | research article | |
dc.volume.number | 42 | |
dspace.entity.type | Publication |