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1.
Ann Otol Rhinol Laryngol ; 110(4): 305-11, 2001 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-11307904

RESUMO

Rarely, patients develop severe idiopathic subglottic stenosis. In 34 years, we have observed this disorder in 52 patients. All but 1 of the patients were female--a finding that suggests a hormonal cause. Without treatment, the airway progressively narrows--in some cases, until the patient requires tracheotomy. Laser submucosal resection and rotation mucosal flaps open and stabilize the airway and provide effective palliation. However, unlike traumatic subglottic stenosis, which has been cured with this technique, the idiopathic form causes submucosal fibrosis that regenerates spontaneously. Thus, treatment helps, but does not cure, the patient. The characteristic pathological finding is of submucosal dense fibrotic tissue with evidence of chronic inflammation. The clinical findings and treatment are here discussed.


Assuntos
Laringoestenose/diagnóstico , Laringoestenose/cirurgia , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Cartilagem Cricoide/cirurgia , Progressão da Doença , Feminino , Fibrose/diagnóstico , Seguimentos , Humanos , Mucosa Laríngea/transplante , Laringoscopia/métodos , Terapia a Laser , Masculino , Pessoa de Meia-Idade , Cuidados Paliativos , Estudos Retrospectivos , Retalhos Cirúrgicos , Traqueotomia
2.
Laryngoscope ; 111(3): 399-403, 2001 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-11224767

RESUMO

HYPOTHESIS: Fungi have been increasingly recognized as important pathogens in sinusitis. However, detection of fungus with conventional culture techniques is insensitive and unreliable. Polymerase chain reaction (PCR) is an exquisitely sensitive assay that can detect the DNA of 10 or less fungal elements. The aim of this study was to compare the sensitivity of conventional culture techniques using PCR analysis. METHODS: Nasal swabs and DNA samples were collected from the nasal cavities of control subjects and patients with chronic sinusitis. Fungal-specific PCR analysis and standard cultures were performed on every sample. chi2 analysis was used to test for statistical differences between groups. RESULTS: PCR analysis detected fungal DNA in 42% and 40% of control subjects and patients with chronic sinusitis while standard cultures were positive in 7% and 0%, respectively. There was no statistically significant difference in the prevalence of fungi in the normal volunteers and patients with chronic rhinosinusitis. CONCLUSION: PCR is significantly more sensitive than nasal swab cultures in detecting the presence of fungi in nasal mucosa. In addition, our study suggests that the presence of fungi alone is insufficient to implicate it as the pathogen in chronic sinusitis.


Assuntos
DNA Fúngico/análise , Fungos/isolamento & purificação , Mucosa Nasal/microbiologia , Reação em Cadeia da Polimerase , Doença Crônica , Humanos , Sinusite/microbiologia
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