Hereditary Gingival Fibromatosis: Report of a Five‐Generation Family Using Cellular Proliferation Analysis

Background: Hereditary gingival fibromatosis (HGF) is an uncommon condition characterized by an accumulation of extracellular matrix resulting in a fibrotic enlargement of the gingiva. The goal of this article is to describe one kindred affected with HGF and discuss the diagnosis, treatment, and con...

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Veröffentlicht in:Journal of periodontology (1970) 2005-12, Vol.76 (12), p.2299-2305
Hauptverfasser: Martelli‐Junior, H., Lemos, D.P., Silva, C.O., Graner, E., Coletta, R.D.
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container_end_page 2305
container_issue 12
container_start_page 2299
container_title Journal of periodontology (1970)
container_volume 76
creator Martelli‐Junior, H.
Lemos, D.P.
Silva, C.O.
Graner, E.
Coletta, R.D.
description Background: Hereditary gingival fibromatosis (HGF) is an uncommon condition characterized by an accumulation of extracellular matrix resulting in a fibrotic enlargement of the gingiva. The goal of this article is to describe one kindred affected with HGF and discuss the diagnosis, treatment, and control of the disease. The pattern of inheritance, histopathologic characteristics, and proliferative potential of epithelial and mesenchymal cells of HGF are also emphasized. Methods: To characterize the pattern of inheritance and the clinical appearance of gingival overgrowth, 117 family members were examined. The recurrence risk was estimated by the use of a genetic analysis program. Immunohistochemistry against the proliferating cell nuclear antigen (PCNA) and pKi‐67 was performed to assess cellular proliferation of normal gingiva (NG) and HGF cells. Results: Examination of the family pedigree demonstrated an autosomal dominant trait of inheritance, and a sibling recurrence risk of 0.085 and an offspring recurrence risk of 0.078, indicating that HGF was a consequence of genetic alteration with low penetrance. Unaffected and affected members transmitted the disease to their offspring. The affected patients showed a generalized but mild gingival overgrowth. Surgical treatment consisted of a combination of gingivectomy and gingivoplasty. Histologic examination showed that the gingival lesions of all patients were quite similar, with increased amounts of collagen fiber bundles in the connective tissue. Immunohistochemistry revealed that the proliferative potential of epithelial cells was significantly higher in the HGF group compared to the NG group, whereas mesenchymal cells from both groups were negative for the proliferative markers. Conclusion: Our data demonstrated that, in the studied family, HGF is transmitted by an autosomal dominant pattern with incomplete disease penetrance, and although the gingival enlargement resulted from an excessive accumulation of collagen fibers, HGF is characterized by an increase in the proliferation rate of epithelial cells.
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The goal of this article is to describe one kindred affected with HGF and discuss the diagnosis, treatment, and control of the disease. The pattern of inheritance, histopathologic characteristics, and proliferative potential of epithelial and mesenchymal cells of HGF are also emphasized. Methods: To characterize the pattern of inheritance and the clinical appearance of gingival overgrowth, 117 family members were examined. The recurrence risk was estimated by the use of a genetic analysis program. Immunohistochemistry against the proliferating cell nuclear antigen (PCNA) and pKi‐67 was performed to assess cellular proliferation of normal gingiva (NG) and HGF cells. Results: Examination of the family pedigree demonstrated an autosomal dominant trait of inheritance, and a sibling recurrence risk of 0.085 and an offspring recurrence risk of 0.078, indicating that HGF was a consequence of genetic alteration with low penetrance. Unaffected and affected members transmitted the disease to their offspring. The affected patients showed a generalized but mild gingival overgrowth. Surgical treatment consisted of a combination of gingivectomy and gingivoplasty. Histologic examination showed that the gingival lesions of all patients were quite similar, with increased amounts of collagen fiber bundles in the connective tissue. Immunohistochemistry revealed that the proliferative potential of epithelial cells was significantly higher in the HGF group compared to the NG group, whereas mesenchymal cells from both groups were negative for the proliferative markers. Conclusion: Our data demonstrated that, in the studied family, HGF is transmitted by an autosomal dominant pattern with incomplete disease penetrance, and although the gingival enlargement resulted from an excessive accumulation of collagen fibers, HGF is characterized by an increase in the proliferation rate of epithelial cells.</description><identifier>ISSN: 0022-3492</identifier><identifier>EISSN: 1943-3670</identifier><identifier>DOI: 10.1902/jop.2005.76.12.2299</identifier><identifier>PMID: 16332243</identifier><language>eng</language><publisher>United States: American Academy of Periodontology</publisher><subject>Autosomal dominant ; Cell Proliferation ; Collagen ; Connective Tissue - pathology ; Dentistry ; Epithelial Cells - pathology ; Female ; Fibromatosis, Gingival - genetics ; Fibromatosis, Gingival - pathology ; Fibromatosis, Gingival - prevention &amp; control ; Genes, Dominant - genetics ; Gingiva - pathology ; Gingivectomy ; Gingivoplasty ; hereditary gingival fibromatosis ; Humans ; Ki-67 Antigen - analysis ; Male ; Mesoderm - pathology ; Pedigree ; Penetrance ; Proliferating Cell Nuclear Antigen - analysis ; proliferation ; Recurrence ; Risk Factors</subject><ispartof>Journal of periodontology (1970), 2005-12, Vol.76 (12), p.2299-2305</ispartof><rights>2005 American Academy of Periodontology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4489-270c2025865ca5d10da409eac23ef28b021394f16baae07ae2623f66743c11c93</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1902%2Fjop.2005.76.12.2299$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1902%2Fjop.2005.76.12.2299$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16332243$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Martelli‐Junior, H.</creatorcontrib><creatorcontrib>Lemos, D.P.</creatorcontrib><creatorcontrib>Silva, C.O.</creatorcontrib><creatorcontrib>Graner, E.</creatorcontrib><creatorcontrib>Coletta, R.D.</creatorcontrib><title>Hereditary Gingival Fibromatosis: Report of a Five‐Generation Family Using Cellular Proliferation Analysis</title><title>Journal of periodontology (1970)</title><addtitle>J Periodontol</addtitle><description>Background: Hereditary gingival fibromatosis (HGF) is an uncommon condition characterized by an accumulation of extracellular matrix resulting in a fibrotic enlargement of the gingiva. The goal of this article is to describe one kindred affected with HGF and discuss the diagnosis, treatment, and control of the disease. The pattern of inheritance, histopathologic characteristics, and proliferative potential of epithelial and mesenchymal cells of HGF are also emphasized. Methods: To characterize the pattern of inheritance and the clinical appearance of gingival overgrowth, 117 family members were examined. The recurrence risk was estimated by the use of a genetic analysis program. Immunohistochemistry against the proliferating cell nuclear antigen (PCNA) and pKi‐67 was performed to assess cellular proliferation of normal gingiva (NG) and HGF cells. Results: Examination of the family pedigree demonstrated an autosomal dominant trait of inheritance, and a sibling recurrence risk of 0.085 and an offspring recurrence risk of 0.078, indicating that HGF was a consequence of genetic alteration with low penetrance. Unaffected and affected members transmitted the disease to their offspring. The affected patients showed a generalized but mild gingival overgrowth. Surgical treatment consisted of a combination of gingivectomy and gingivoplasty. Histologic examination showed that the gingival lesions of all patients were quite similar, with increased amounts of collagen fiber bundles in the connective tissue. Immunohistochemistry revealed that the proliferative potential of epithelial cells was significantly higher in the HGF group compared to the NG group, whereas mesenchymal cells from both groups were negative for the proliferative markers. Conclusion: Our data demonstrated that, in the studied family, HGF is transmitted by an autosomal dominant pattern with incomplete disease penetrance, and although the gingival enlargement resulted from an excessive accumulation of collagen fibers, HGF is characterized by an increase in the proliferation rate of epithelial cells.</description><subject>Autosomal dominant</subject><subject>Cell Proliferation</subject><subject>Collagen</subject><subject>Connective Tissue - pathology</subject><subject>Dentistry</subject><subject>Epithelial Cells - pathology</subject><subject>Female</subject><subject>Fibromatosis, Gingival - genetics</subject><subject>Fibromatosis, Gingival - pathology</subject><subject>Fibromatosis, Gingival - prevention &amp; control</subject><subject>Genes, Dominant - genetics</subject><subject>Gingiva - pathology</subject><subject>Gingivectomy</subject><subject>Gingivoplasty</subject><subject>hereditary gingival fibromatosis</subject><subject>Humans</subject><subject>Ki-67 Antigen - analysis</subject><subject>Male</subject><subject>Mesoderm - pathology</subject><subject>Pedigree</subject><subject>Penetrance</subject><subject>Proliferating Cell Nuclear Antigen - analysis</subject><subject>proliferation</subject><subject>Recurrence</subject><subject>Risk Factors</subject><issn>0022-3492</issn><issn>1943-3670</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkMFOGzEQhq2qVUmBJ6iEfOptF3vs9a65oYiEIqQiBGfL2cxWRt51sDeg3HgEnrFPUocEceVkjfz9v2Y-Qn5yVnLN4PQhrEpgrCprVXIoAbT-QiZcS1EIVbOvZMIYQCGkhgPyI6WHPHIp2HdywJUQAFJMiL_EiEs32rihczf8dU_W05lbxNDbMSSXzugtrkIcaeiozT9P-O_ldY4DRju6MNCZ7Z3f0PuUw3SK3q-9jfQmBu-6d-Z8sH6Tu47It876hMf795Dczy7uppfF9Z_57-n5ddFK2egCatYCg6pRVWurJWdLK5lG24LADppFPkNo2XG1sBZZbREUiE6pWoqW81aLQ_Jr17uK4XGNaTS9S23ezQ4Y1smopqmhYltQ7MA2hpQidmYVXZ9dGM7MVrLJks1WsqmV4WC2knPqZF-_XvS4_MjsrWZA74Bn53HzmU5zdXNx-1b-H9cui8I</recordid><startdate>200512</startdate><enddate>200512</enddate><creator>Martelli‐Junior, H.</creator><creator>Lemos, D.P.</creator><creator>Silva, C.O.</creator><creator>Graner, E.</creator><creator>Coletta, R.D.</creator><general>American Academy of Periodontology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200512</creationdate><title>Hereditary Gingival Fibromatosis: Report of a Five‐Generation Family Using Cellular Proliferation Analysis</title><author>Martelli‐Junior, H. ; 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The goal of this article is to describe one kindred affected with HGF and discuss the diagnosis, treatment, and control of the disease. The pattern of inheritance, histopathologic characteristics, and proliferative potential of epithelial and mesenchymal cells of HGF are also emphasized. Methods: To characterize the pattern of inheritance and the clinical appearance of gingival overgrowth, 117 family members were examined. The recurrence risk was estimated by the use of a genetic analysis program. Immunohistochemistry against the proliferating cell nuclear antigen (PCNA) and pKi‐67 was performed to assess cellular proliferation of normal gingiva (NG) and HGF cells. Results: Examination of the family pedigree demonstrated an autosomal dominant trait of inheritance, and a sibling recurrence risk of 0.085 and an offspring recurrence risk of 0.078, indicating that HGF was a consequence of genetic alteration with low penetrance. Unaffected and affected members transmitted the disease to their offspring. The affected patients showed a generalized but mild gingival overgrowth. Surgical treatment consisted of a combination of gingivectomy and gingivoplasty. Histologic examination showed that the gingival lesions of all patients were quite similar, with increased amounts of collagen fiber bundles in the connective tissue. Immunohistochemistry revealed that the proliferative potential of epithelial cells was significantly higher in the HGF group compared to the NG group, whereas mesenchymal cells from both groups were negative for the proliferative markers. Conclusion: Our data demonstrated that, in the studied family, HGF is transmitted by an autosomal dominant pattern with incomplete disease penetrance, and although the gingival enlargement resulted from an excessive accumulation of collagen fibers, HGF is characterized by an increase in the proliferation rate of epithelial cells.</abstract><cop>United States</cop><pub>American Academy of Periodontology</pub><pmid>16332243</pmid><doi>10.1902/jop.2005.76.12.2299</doi><tpages>7</tpages></addata></record>
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subjects Autosomal dominant
Cell Proliferation
Collagen
Connective Tissue - pathology
Dentistry
Epithelial Cells - pathology
Female
Fibromatosis, Gingival - genetics
Fibromatosis, Gingival - pathology
Fibromatosis, Gingival - prevention & control
Genes, Dominant - genetics
Gingiva - pathology
Gingivectomy
Gingivoplasty
hereditary gingival fibromatosis
Humans
Ki-67 Antigen - analysis
Male
Mesoderm - pathology
Pedigree
Penetrance
Proliferating Cell Nuclear Antigen - analysis
proliferation
Recurrence
Risk Factors
title Hereditary Gingival Fibromatosis: Report of a Five‐Generation Family Using Cellular Proliferation Analysis
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