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1.
Rev Stomatol Chir Maxillofac ; 110(1): e1-4, 2009 Feb.
Artículo en Francés | MEDLINE | ID: mdl-19108856

RESUMEN

INTRODUCTION: Sialendoscopy and sialo-MRI enable diagnosis of salivary gland obstructive pathologies, such as lithiasis, stenosis and dilatations. Therefore, a classification of these pathologies is needed, allowing large series comparisons, for better diagnosis and treatment of salivary pathologies. MATERIAL AND METHODS: With help from people from the European Sialendoscopy Training Center (ESTC), the results of sialographies, sialoMRI and sialendoscopies, a comprehensive classification of obstructive salivary pathologies is described, based on the absence or presence of lithiasis (L), stenosis (S) and dilatation (D) ("LSD" classification). DISCUSSION: It appears that a classification of salivary gland obstructive pathologies should be described. We hope it will be widely used and of course criticized to be improved and to compare the results of salivary gland diagnostic methods, such as sialography and sialendoscopy and also the results and indications for salivary gland therapeutic methods, such as lithotripsy, sialendoscopy and/or open surgery.


Asunto(s)
Cálculos del Conducto Salival/clasificación , Cálculos de las Glándulas Salivales/clasificación , Enfermedades de las Glándulas Salivales/clasificación , Constricción Patológica/clasificación , Dilatación Patológica/clasificación , Endoscopía , Humanos , Imagen por Resonancia Magnética , Conductos Salivales/patología , Sialografía
2.
Rev Stomatol Chir Maxillofac ; 109(4): 233-6, 2008 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-18774150

RESUMEN

INTRODUCTION: Sialendoscopy and sialoMRI enables diagnosis of salivary gland obstructive pathologies, such as lithiasis, stenosis, and dilatations. Therefore, a classification of these pathologies is needed, allowing large series comparisons, for better diagnosis and treatment of salivary pathologies. MATERIAL AND METHODS: With help from people from the European Sialendoscopy Training Center (ESTC), the results of sialographies, sialoMRI and sialendoscopies, a comprehensive classification of obstructive salivary pathologies is described, based on the absence or presence of lithiasis (L), stenosis (S), and dilatation (D) ("LSD" classification). DISCUSSION: It appears that a classification of salivary gland obstructive pathologies should be described. We hope it will be widely used and of course criticized to be improved and to compare the results of salivary gland diagnostic methods, such as sialography and sialendoscopy, and also the results and indications for salivary gland therapeutic methods, such as lithotripsy, sialendoscopy, and/or open surgery.


Asunto(s)
Cálculos de las Glándulas Salivales/clasificación , Enfermedades de las Glándulas Salivales/clasificación , Constricción Patológica/clasificación , Dilatación Patológica/clasificación , Endoscopía , Humanos , Imagen por Resonancia Magnética , Cálculos del Conducto Salival/clasificación , Conductos Salivales/patología , Sialografía
3.
J Otolaryngol ; 26(4): 225-8, 1997 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-9263889

RESUMEN

OBJECTIVE: The purpose of this study was to compare reasons for family physician (FP) referral of children for tonsillectomy to the indications for this surgery used by otolaryngologists practising in the same region. METHOD: A checklist-type survey was sent to a random sample of 300 FPs and all of the practising otolaryngologists in Nova Scotia in the spring of 1995. RESULTS: There were significant differences between reasons for referral and indications for treatment in many areas, the most important of which was that over 60% of FPs referred cases because of parental insistence, while no surgeons operated for this reason. If inappropriate referrals are taken to be those for which no specialist intervention occurs, it appears that there is a significant number of referrals. CONCLUSION: These results suggest that both FPs and parents require information about these common paediatric problems.


Asunto(s)
Medicina Familiar y Comunitaria , Otolaringología , Derivación y Consulta , Tonsilectomía , Adolescente , Adulto , Niño , Preescolar , Humanos , Lactante , Recién Nacido , Persona de Mediana Edad
5.
Thyroid ; 6(5): 409-16, 1996 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-8936664

RESUMEN

Ras proteins are signal-transducing proteins that share common properties with membrane-anchored G proteins. Mutations at codon 12/13 or codon 61 alter GTP-binding or GTPase activity, respectively. Such activating mutations are present in nearly 30-50% of various malignancies including colon, breast, and lung carcinomas. There are conflicting data regarding the prevalence of ras mutations in the thyroid and their possible pathogenetic role in the different tumor types. To address this question, we examined 45 morphologically characterized thyroid carcinomas, adenomas, and hyperplastic nodules using a highly sensitive single-stranded conformation polymorphism (SSCP) approach combined with DNA-sequencing. DNA from cell lines with known mutations served as controls. A G to A H13 codon substitution replacing an Asp for a Gly residue was detected in 1 papillary carcinoma. Although no H12 or H61 codon substitutions were identified, 2 discrete alterations were identified in codons H17 and 22. No N12/13 codon substitutions were identified. N61 codon substitutions of A to G resulting in a Gly to Arg substitution were detected in 2 papillary carcinomas; the same mutation was also found in one follicular adenoma. Interestingly, K12/13 and K61 ras mutations were not present in any of the tumors examined. These data establish a low prevalence of mutations in all ras gene family members in human thyroid neoplasms. This difference from neoplasms of other organs may explain the relatively indolent biologic behavior of many thyroid tumors and supports an alternate early genetic mutation that is more characteristic of these neoplasms.


Asunto(s)
Genes ras , Mutación , Neoplasias de la Tiroides/genética , Nódulo Tiroideo/genética , Adulto , Anciano , Anciano de 80 o más Años , Secuencia de Bases , Codón/genética , ADN/genética , Cartilla de ADN/genética , ADN de Neoplasias/genética , Femenino , Humanos , Masculino , Persona de Mediana Edad , Mutación Puntual , Reacción en Cadena de la Polimerasa , Polimorfismo Conformacional Retorcido-Simple , Análisis de Secuencia de ADN , Neoplasias de la Tiroides/patología , Nódulo Tiroideo/patología
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