Minichromosome maintenance 2 and 5 expressions are increased in the epithelium of hereditary gingival fibromatosis associated with dental abnormalities.

INTRODUCTION: Gingiva fibromatosis is a relatively rare condition characterized by diffuse enlargement of the gingiva, which is caused by expansion and accumulation of the connective tissue. OBJECTIVE: The aim of the present study was to investigate proliferative and apoptotic biomarker expression in normal gingiva and two forms of gingival fibromatosis. METHODS: Archived tissue specimens of hereditary gingival fibromatosis, gingival fibromatosis and dental abnormality syndrome and normal gingiva were subject to morphological analysis and immunohistochemical staining. The results were analyzed statistically. RESULTS: Proteins associated with proliferation were found in the nuclei of epithelial cells from the basal and suprabasal layers, whereas apoptotic proteins were detected in the cytoplasm of the upper layers of the epithelium. Increased expressions of minichromosome maintenance proteins 2 and 5 were observed in the gingival fibromatosis and dental abnormality syndrome samples. In contrast, geminin expression was higher in normal gingiva samples. No difference in the expression of apoptotic proteins was observed among the groups. CONCLUSION: Our findings support a role for augmented proliferation of epithelial cells within the overgrown tissues associated with gingival fibromatosis or dental abnormality syndrome. However, our data suggest that different biological mechanisms may account for the pathogenesis of different types of gingival fibromatosis.

Minichromosome maintenance 2 and 5 expressions are increased in the epithelium of hereditary gingival fibromatosis associated with dental abnormalities

INTRODUCTION: Gingiva fibromatosis is a relatively rare condition characterized by diffuse enlargement of the gingiva, which is caused by expansion and accumulation of the connective tissue. OBJECTIVE: The aim of the present study was to investigate proliferative and apoptotic biomarker expression in normal gingiva and two forms of gingival fibromatosis. METHODS: Archived tissue specimens of hereditary gingival fibromatosis, gingival fibromatosis and dental abnormality syndrome and normal gingiva were subject to morphological analysis and immunohistochemical staining. The results were analyzed statistically. RESULTS: Proteins associated with proliferation were found in the nuclei of epithelial cells from the basal and suprabasal layers, whereas apoptotic proteins were detected in the cytoplasm of the upper layers of the epithelium. Increased expressions of minichromosome maintenance proteins 2 and 5 were observed in the gingival fibromatosis and dental abnormality syndrome samples. In contrast, geminin expression was higher in normal gingiva samples. No difference in the expression of apoptotic proteins was observed among the groups. CONCLUSION: Our findings support a role for augmented proliferation of epithelial cells within the overgrown tissues associated with gingival fibromatosis or dental abnormality syndrome. However, our data suggest that different biological mechanisms may account for the pathogenesis of different types of gingival fibromatosis.

Myositis ossificans traumatica of the medial pterygoid muscle: a case report.

In this report, we present a case of myositis ossificans traumatica (MOT) of the medial pterygoid muscle that had developed after mandibular block anesthesia administered for endodontic treatment of the lower right second molar, demonstrating typical features of this condition. MOT should be considered as a differential diagnosis when there is severe limitation of jaw opening and an associated trauma. Panoramic radiographs and axial and coronal computed tomography (CT) scans can effectively delineate the calcified mass. Other imaging studies that may be helpful include magnetic resonance imaging (MRI), bone scans, and ultrasound. As shown in our case, calcified masses were found in the right mandibular angle, which severely limited jaw opening. Some earlier reported cases of MOT were treated by extraoral surgical approaches with complete removal of the evolving muscle. The aim of this case report is to present only the diagnostic imaging aspects of myositis ossificans traumatica.

Avaliação do espaço aéreo faríngeo por meio da tomografia computadorizada de feixe cônico / Assessment of pharyngeal airway space using Cone-Beam Computed Tomography

INTRODUÇÃO: a avaliação do espaço aéreo superior faz parte da rotina na elaboração do diagnóstico e plano de tratamento ortodôntico. A radiografia cefalométrica em norma lateral tem sido usada rotineiramente na avaliação da permeabilidade do espaço aéreo, esbarrando na limitação de fornecer uma imagem bidimensional de uma estrutura tridimensional. A Tomografia Computadorizada de Feixe Cônico (TCFC) tem entrado na realidade ortodôntica trazendo um arsenal de informações concernentes ao espaço aéreo superior. Por fornecer uma imagem tridimensional, possibilita determinar de maneira precisa a área de maior estreitamento da faringe, que ofereceria maior resistência à passagem aérea. OBJETIVOS: o propósito deste artigo é esclarecer o ortodontista quanto aos recursos disponíveis na TCFC para o diagnóstico de possíveis barreiras físicas que possam diminuir a permeabilidade das vias aéreas superiores.

INTRODUCTION: Evaluation of upper airway space is a routine procedure in orthodontic diagnosis and treatment planning. Although limited insofar as they provide two dimensional images of three-dimensional structures, lateral cephalometric radiographs have been used routinely to assess airway space permeability. Cone-Beam Computed Tomography (CBCT) has contributed to orthodontics with information concerning the upper airway space. By producing three-dimensional images CBCT allows professionals to accurately determine the most constricted area, where greater resistance to air passage occurs. OBJECTIVES: The purpose of this article is to enlighten orthodontists on the resources provided by CBCT in the diagnosis of possible physical barriers that can reduce upper airway permeability.