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2.
Med Oral Patol Oral Cir Bucal ; 17(6): e1028-33, 2012 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-22549668

RESUMO

OBJECTIVES: The goal of the present study was to evaluate the results of applying acupuncture or occlusal decompression splints in the treatment of patients diagnosed with the temporomandibular joint pain-dysfunction syndrome. DESIGN OF THE STUDY: We conducted a randomized clinical trial including 20 patients to whom the mentioned treatments were applied. Results were evaluated through an analogue pain scale, measurements of mouth opening and jaw lateral deviation in millimetres, and assessment of sensitivity to pressure on different points: preauricular, masseter muscle, temporal muscle and trapezius. Parameters were evaluated before and 30 days after the treatment. For standardized pressure, we used a pressure algometer. RESULTS: Patients treated with decompression splints showed reductions in subjective pain and pain upon pressure on temporal, masseter and trapezius muscles, as well as increased mouth opening after the treatment. Patients treated with acupuncture showed pain reduction in the short term and improvements in all of the evaluated para-meters (stronger pressure was required to produce pain; mouth opening was improved). CONCLUSION: Acupuncture was an effective complement and/or an acceptable alternative to decompression splints in the treatment of myofascial pain and temporomandibular joint pain-dysfunction syndrome.


Assuntos
Terapia por Acupuntura , Descompressão Cirúrgica , Síndrome da Disfunção da Articulação Temporomandibular/terapia , Adolescente , Adulto , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Adulto Jovem
3.
Med Oral Patol Oral Cir Bucal ; 11(4): E319-24, 2006 Jul 01.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-16816815

RESUMO

Cowden syndrome is a rare hereditary disease included within hamartoma-type gastrointestinal polyposis. It is characterised by associated mucocutaneous anomalies and by the extraordinary tendency to develop malignant neoplasia, mainly in the breast and thyroid. Early diagnosis of the syndrome and adequate tumoral screening in patients with mucocutaneous papillomatosis make it possible to make an earlier diagnosis of associated pathologies which have great morbidity when detected late. We present the case of a patient diagnosed with Cowden syndrome after consultation for labial papillomatous lesions of long evolution who was subsequently treated for breast and kidney cancer in initial stages. The correct diagnosis of a banal pathology of oral mucosa made it possible for us to take early action against the neoplastic pathology associated with this disease.


Assuntos
Síndrome do Hamartoma Múltiplo/diagnóstico , Neoplasias Bucais/diagnóstico , Papiloma/diagnóstico , Adulto , Feminino , Humanos
4.
Med. oral patol. oral cir. bucal (Internet) ; 11(4): E319-E324, jul. 2006. ilus, tab
Artigo em Es | IBECS | ID: ibc-047002

RESUMO

El síndrome de Cowden es una infrecuente enfermedad hereditaria englobada dentro de las poliposis gastrointestinales de tipo hamartomatoso. Se caracteriza por asociar anomalías cutaneomucosas y por la extraordinaria tendencia a desarrollar neoplasias malignas, principalmente de mama y tiroides. La importancia de un diagnóstico precoz del síndrome y de un adecuado screening tumoral en pacientes con lesiones papilomatosas cutaneomucosas, nos va a permitir adelantarnos en el diagnóstico de patologías con enorme morbimortalidad asociada en caso de una detección tardía. Presentamos el caso de una paciente diagnosticada de síndrome de Cowden tras consultar por lesiones papilomatosas labiales de largo tiempo de evolución y tratada posteriormente de cáncer de mama y riñón en estadios iniciales. El correcto diagnóstico de una patología banal de mucosa oral, nos ha permitido actuar de manera muy precoz frente a la patología neoplásica asociada a dicha enfermedad


Cowden syndrome is a rare hereditary disease included within hamartoma-type gastrointestinal polyposis. It is characterisedby associated mucocutaneous anomalies and by the extraordinary tendency to develop malignant neoplasia, mainly in the breast and thyroid. Early diagnosis of the syndrome and adequate tumoral screening in patients with mucocutaneous papillomatosis make it possible to make an earlier diagnosis of associated pathologies which have great morbidity when detected late. We present the case of a patient diagnosed with Cowden syndrome after consultation for labial papillomatous lesions of long evolution who was subsequently treated for breast and kidney cancer in initial stages.The correct diagnosis of a banal pathology of oral mucosa made it possible for us to take early action against the neoplasticpathology associated with this disease


Assuntos
Feminino , Adulto , Humanos , Síndrome do Hamartoma Múltiplo/diagnóstico , Papiloma/diagnóstico , Neoplasias Bucais/diagnóstico
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