Volume 32, Issue 10 pp. 1116-1121

Morphological and molecular analysis of idiopathic gingival fibromatosis: a case report

Nicoletta Gagliano

Nicoletta Gagliano

Department of Human Morphology-LITA Segrate, University of Milan, Milan, Italy

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Claudia Moscheni

Claudia Moscheni

Department of Human Morphology-LITA Segrate, University of Milan, Milan, Italy

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Claudia Dellavia

Claudia Dellavia

Department of Human Morphology, University of Milan, Milan, Italy

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Silvia Masiero

Silvia Masiero

Private periodontal practice, Saronno (VA), Italy

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Carlo Torri

Carlo Torri

Department of Human Morphology-LITA Segrate, University of Milan, Milan, Italy

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Fabio Grizzi

Fabio Grizzi

Scientific Direction, Istituto Clinico Humanitas, Rozzano and “M. Rodriguez” Foundation, Institute for Quantitative Measures in Medicine, Milan, Italy

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Giordano Stabellini

Giordano Stabellini

Department of Human Morphology-LITA Segrate, University of Milan, Milan, Italy

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Magda Gioia

Magda Gioia

Department of Human Morphology-LITA Segrate, University of Milan, Milan, Italy

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First published: 08 September 2005
Citations: 19
Address:
Nicoletta Gagliano
Department of Human Morphology- LITA
University of Milan
Via Fratelli Cervi 93
20090 Segrate, Milan
Italy
E-mail: [email protected]

Abstract

Aim: We analyse a case of idiopathic gingival overgrowth using morphological and molecular methods. As this overgrowth involves collagen accumulation in the gingival connective tissue, we measured the collagen turnover to clarify the pathogenic mechanisms potentially involved.

Materials and Methods: The patient was a 29-year-old Italian woman with enlargement of the gingivae throughout the entire mandible and maxilla. Morphological analyses were carried out on haematoxylin–eosin and Sirius red-stained paraffin-embedded gingival sections. mRNA levels of collagen type I and III, matrix metalloproteinase (MMP)-1, transforming growth factor-β1 and lysyl hydroxylase (LH)2b were determined by RT-PCR on cultured gingival fibroblasts and compared with healthy control fibroblasts. Interstitial collagen and MMP-1 content in the supernatants were assessed, respectively, by dot blot and SDS zymography.

Results and Conclusions: In Sirius red-stained sections of the patient's overgrown gingivae, interstitial collagen content was 29% higher than controls. Her gingival fibroblasts had higher collagen type I, MMP-1 and LH2b gene expression and unmodified interstitial collagen, type I protein levels in the supernatants. These findings would seem to suggest that in this case collagen accumulation in the gingival connective tissue was not associated with increased synthesis and decreased degradation.

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