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1.
Artigo em Inglês | MEDLINE | ID: mdl-19748292

RESUMO

OBJECTIVES: To characterize the clinical manifestations of Actinomyces-associated lesions of the oral mucosa and jawbones, and to correlate the clinical course and treatment requirements with the findings of histomorphometric analysis. STUDY DESIGN: The study was a 10-year retrospective analysis of archived cases with microscopic identification of Actinomyces infection. Actinomyces colonies were identified, using hematoxylin-eosin, Gram, and periodic acid-Schiff stains, exhibiting filamentous morphology with color variation between center and periphery. Only colonies with adjacent tissue reaction (inflammation, fibrosis) were analyzed. Actinomyces density (AD) was calculated by dividing total number of colonies by tissue surface, Actinomyces relative surface (ARS) was calculated by dividing total bacterial surface by tissue surface. RESULTS: The study included 106 cases (48 male, 58 female; aged 13-84 years, mean 50.5 years). Cases presented a wide clinical spectrum, involving jawbone and/or oral soft tissues. Cases included osteomyelitis associated with bisphosphonates, osteoradionecrosis, osteomyelitis unrelated to radiation or bisphosphonates, periapical lesions, odontogenic cysts, periimplantitis, and lesion mimicking periodontal disease. The AD correlated with median length of antibiotic treatment (R = 0.284; P = .028). CONCLUSIONS: Because we were able to identify 106 such cases, the results indicate that Actinomyces-associated lesions may not be as rare as would be expected from the relatively low number of cases in the literature. Actinomyces-associated lesions presented in a wide spectrum of clinical settings and a variety of contributing factors. Quantitative analysis of the number of bacterial colonies (representing bacterial load) could help in evaluating the aggressive potential of the lesion and help in treatment planning.


Assuntos
Actinomicose/patologia , Doenças Maxilomandibulares/patologia , Doenças da Boca/patologia , Actinomicose/tratamento farmacológico , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Antibacterianos/uso terapêutico , Contagem de Colônia Microbiana , Feminino , Granuloma Piogênico/tratamento farmacológico , Granuloma Piogênico/microbiologia , Humanos , Doenças Maxilomandibulares/tratamento farmacológico , Doenças Maxilomandibulares/microbiologia , Masculino , Pessoa de Meia-Idade , Doenças da Boca/tratamento farmacológico , Doenças da Boca/microbiologia , Mucosa Bucal/microbiologia , Mucosa Bucal/patologia , Osteomielite/tratamento farmacológico , Osteomielite/microbiologia , Osteonecrose/tratamento farmacológico , Osteonecrose/microbiologia , Osteorradionecrose/tratamento farmacológico , Osteorradionecrose/microbiologia , Cisto Radicular/tratamento farmacológico , Cisto Radicular/microbiologia , Cisto Radicular/patologia , Estudos Retrospectivos , Adulto Jovem
2.
J Surg Oncol ; 98(8): 572-8, 2008 Dec 15.
Artigo em Inglês | MEDLINE | ID: mdl-18449877

RESUMO

A protocol was created for prospective margin status evaluation of patients with Oral SCC. Margins are evaluated intra- and post-operatively during three stages. Patients were divided into three groups: group 1 in which one margins were sampled randomly, group 2 with frozen sections taken from the surgical bed and 3 in which they were taken from the tumor specimen itself. Patients in group 3 showed the best correlation with final margin status and survival.


Assuntos
Carcinoma de Células Escamosas/patologia , Carcinoma de Células Escamosas/cirurgia , Secções Congeladas/métodos , Neoplasias Bucais/patologia , Neoplasias Bucais/cirurgia , Idoso , Biópsia/métodos , Carcinoma de Células Escamosas/mortalidade , Estudos de Coortes , Intervalo Livre de Doença , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Neoplasias Bucais/mortalidade , Estadiamento de Neoplasias , Estudos Retrospectivos , Resultado do Tratamento , Adulto Jovem
3.
Otolaryngol Head Neck Surg ; 128(2): 196-9, 2003 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-12601314

RESUMO

OBJECTIVE: We sought to define the incidence of neuroma formation after neck dissection in a large series of patients. METHODS: One hundred fifty-three patients who were seen during a 2-year period (followed for 3 months to 10 years; mean, 52 months) were evaluated for neuroma formation after neck dissection (185 procedures). Cut nerve edges were not routinely ligated or cauterized. RESULTS: Operative records indicated that except for 4 cases, the stumps of the great auricular nerve and cervical branches were left intact after resection. No cases of palpable neuromas were found. In one case of a revised neck, a small macroscopically indiscernible nodule was histologically defined as neuroma. CONCLUSION: No neuromas were discovered in our series of neck dissection cases. If found, it is imperative these lesions be differentiated from recurrent cancer. Our results do not support any interference with cut nerve edges.


Assuntos
Carcinoma de Células Escamosas/cirurgia , Neoplasias de Cabeça e Pescoço/cirurgia , Esvaziamento Cervical/métodos , Neuroma Acústico/epidemiologia , Neuroma Acústico/etiologia , Complicações Pós-Operatórias , Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade
4.
J Endod ; 28(1): 30-3, 2002 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-11806645

RESUMO

Wound healing in the oral cavity occurs in a bacteria-rich environment, which may affect its outcome. Furthermore, it takes place where forces are frequently applied to the healing tissue. The effect of bacterial endotoxin on the development of tensile strength in healing wounds was studied using surgical skin wounds in rats as a model. Collagen membranes soaked with 0.01 microg of bacterial endotoxin were inserted into surgical skin wounds, and their effect was studied on days 6 and 10. Membranes with no endotoxin served as controls. Endotoxin inhibited the early development of tensile strength in 6 days, healing wounds by 38%, whereas the collagen membrane alone had no effect. Dexamethasone (0.5 mg/kg every 72 h) had a suppressive effect on the development of tensile strength in healing noncontaminated wounds, but not in those containing bacterial endotoxin. These results suggest that bacterial endotoxin may interfere with the early healing of wounds. Understanding the mechanisms of this inhibition may result in treatments that will allow this response to be faster and more reproducible.


Assuntos
Procedimentos Cirúrgicos Dermatológicos , Endotoxinas/farmacologia , Escherichia coli , Lipopolissacarídeos/farmacologia , Análise de Variância , Animais , Anti-Inflamatórios/farmacologia , Colágeno Tipo I , Dexametasona/farmacologia , Modelos Animais de Doenças , Endotoxinas/antagonistas & inibidores , Seguimentos , Lipopolissacarídeos/antagonistas & inibidores , Masculino , Membranas Artificiais , Ratos , Ratos Sprague-Dawley , Pele/fisiopatologia , Estatística como Assunto , Deiscência da Ferida Operatória/fisiopatologia , Resistência à Tração , Cicatrização/efeitos dos fármacos
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