Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros











Intervalo de ano de publicação
1.
Braz J Otorhinolaryngol ; 80(3): 202-7, 2014.
Artigo em Inglês, Português | MEDLINE | ID: mdl-25153103

RESUMO

INTRODUCTION: Establishing a diagnosis in patients with olfactory disturbances has always been challenging for physicians.One reason for this is the rarity of some of the diseases that affect this sense, such as Kallmann's syndrome and post-viral olfactory loss. OBJECTIVE: To identify the major causes of olfactory disturbances and to describe the diagnostic evaluation in outpatients attended to at an ambulatory clinic specialized in olfaction disorders. METHODS: A retrospective analysis was performed in outpatients with primary olfactory complaint attended to between June 1, 2011 and September 30, 2013 in a center specialized in olfactory disorders. Patient history, nasofibroscopy, and the University of Pennsylvania Smell Identification Test (UPSIT) comprised the examination. RESULTS: Sixty-two patients were evaluated. The major causes were chronic rhinosinusitis (31%); rhinitis, primarily the allergic type (19%); post-viral olfactory loss (13%); and post-traumatic loss (8%). UPSIT scores were statistically different among different etiologies (p = 0.01). CONCLUSIONS: The major diagnoses that should be part of the physician assessment when a patient complains of olfactory disturbance are chronic rhinosinusitis with and without polyps, allergic rhinitis, post-viral olfactory loss, and post-traumatic loss.


Assuntos
Transtornos do Olfato/diagnóstico , Transtornos do Olfato/etiologia , Adulto , Traumatismos Craniocerebrais/complicações , Feminino , Humanos , Masculino , Pólipos Nasais/complicações , Infecções Respiratórias/complicações , Infecções Respiratórias/virologia , Estudos Retrospectivos , Rinite/complicações , Sinusite/complicações
2.
Braz. j. otorhinolaryngol. (Impr.) ; Braz. j. otorhinolaryngol. (Impr.);80(3): 202-207, May-June/2014. tab, graf
Artigo em Inglês | LILACS | ID: lil-712980

RESUMO

INTRODUCTION: Establishing a diagnosis in patients with olfactory disturbances has always been challenging for physicians.One reason for this is the rarity of some of the diseases that affect this sense, such as Kallmann's syndrome and post-viral olfactory loss. OBJECTIVE: To identify the major causes of olfactory disturbances and to describe the diagnostic evaluation in outpatients attended to at an ambulatory clinic specialized in olfaction disorders. METHODS: A retrospective analysis was performed in outpatients with primary olfactory complaint attended to between June 1, 2011 and September 30, 2013 in a center specialized in olfactory disorders. Patient history, nasofibroscopy, and the University of Pennsylvania Smell Identification Test (UPSIT) comprised the examination. RESULTS: Sixty-two patients were evaluated. The major causes were chronic rhinosinusitis (31%); rhinitis, primarily the allergic type (19%); post-viral olfactory loss (13%); and post-traumatic loss (8%). UPSIT scores were statistically different among different etiologies (p = 0.01). CONCLUSIONS: The major diagnoses that should be part of the physician assessment when a patient complains of olfactory disturbance are chronic rhinosinusitis with and without polyps, allergic rhinitis, post-viral olfactory loss, and post-traumatic loss. .


INTRODUÇÃO: Estabelecer um diagnóstico em pacientes com distúrbios olfatórios foi sempre um desafio aos médicos. Uma das razões para isso é a raridade de algumas doenças que afetam esse sentido como a Síndrome de Kallmann e a perda olfatória pós-viral. OBJETIVO: Identificar as principais causas das doenças olfatórias e descrever sua condução diagnóstica em um ambulatório direcionado a esses distúrbios. MÉTODO: Análise retrospectiva de pacientes ambulatoriais com queixa olfatória primária atendida entre 1º de junho de 2011 e 30 de setembro de 2013 em centro especializado. História clínica, nasofibroscopia e o Teste de Identificação do Olfato da Universidade da Pensilvânia (UPSIT) compuseram a avaliação. Sempre que necessário, foram solicitadas tomografia de seios paranasais e ressonância magnética de crânio. RESULTADOS: Sessenta e dois pacientes foram avaliados. As causas mais comuns encontradas foram respectivamente: rinossinusite crônica (31%), rinites (19%), principalmente a rinite alérgica, perda olfatória pós-viral (13%) e pós-traumática (8%). As pontuações no UPSIT foram estatisticamente diferentes entre as cinco principais causas (p = 0,01). CONCLUSÕES: Os principais diagnósticos que devem fazer parte na investigação médica diante de um paciente com queixa olfatória são: rinossinusite crônica com e sem polipose nasal, rinite alérgica, perda olfatória pós-viral e pós-traumática. .


Assuntos
Adulto , Feminino , Humanos , Masculino , Transtornos do Olfato/diagnóstico , Transtornos do Olfato/etiologia , Traumatismos Craniocerebrais/complicações , Pólipos Nasais/complicações , Estudos Retrospectivos , Infecções Respiratórias/complicações , Infecções Respiratórias/virologia , Rinite/complicações , Sinusite/complicações
3.
Int Forum Allergy Rhinol ; 2(6): 501-6, 2012 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-22566483

RESUMO

BACKGROUND: Giant cell tumors of bone (GCTs) are common in the long bones, but rare in the craniofacial region, with only 1% of cases occurring in the latter. Clinical, radiological, and anatomical diagnosis of this locally aggressive disease, which occurs in response to trauma or neoplastic transformation, poses a major challenge in clinical practice. METHODS: The present study describes a series of 4 cases and highlights the main features of the differential diagnosis and treatment of these lesions: GCT, giant cell reparative granuloma (GCRG), and the brown tumor of hyperparathyroidism. RESULTS: GCT presents as a benign neoplasm, most typically affecting the knees, and rarely in the temporal and sphenoid bones. It is radiologically indistinguishable from GCRG due to its lytic, poorly defined appearance. The distinction can only be made microscopically, as the presence of multinucleated giant cells scattered throughout the stroma and the absence of a history of trauma favor a diagnosis of GCT. The brown tumor of hyperparathyroidism occurs with rapid, localized osteoclast activity secondary to the effects of increased parathyroid hormone (PTH) levels; parathyroid examination is indispensable. CONCLUSION: The diagnosis and treatment of these lesions poses a major challenge due to their similar clinical presentation and radiological appearance. Accurate diagnosis is essential for definition of appropriate management, as complete resection is the goal in GCT and GCRG to avoid recurrence, whereas the brown tumor often yields to treatment of the underlying hyperparathyroidism.


Assuntos
Ossos Faciais , Tumor de Células Gigantes do Osso/diagnóstico , Granuloma de Células Gigantes/diagnóstico , Neoplasias Cranianas/diagnóstico , Adulto , Idoso , Criança , Diagnóstico Diferencial , Feminino , Tumor de Células Gigantes do Osso/cirurgia , Granuloma de Células Gigantes/cirurgia , Humanos , Pessoa de Meia-Idade , Neoplasias Cranianas/cirurgia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA