Assuntos
Linfoma de Burkitt/diagnóstico , Infecções por Mycobacterium/diagnóstico , Mycobacterium bovis/fisiologia , Proteínas Serina-Treonina Quinases/genética , Deleção de Sequência/genética , Linfoma de Burkitt/genética , Criança , Pré-Escolar , Consanguinidade , Eczema , Evolução Fatal , Sequenciamento de Nucleotídeos em Larga Escala , Humanos , Peptídeos e Proteínas de Sinalização Intracelular , Masculino , Infecções por Mycobacterium/genética , Otite Média , Linhagem , Infecções RespiratóriasRESUMO
INTRODUCTION: We assessed the yield of high-resolution ultrasonography (HRUS) in patients with clinically definite carpal tunnel syndrome (CTS) and normal nerve conduction studies (NCS). METHODS: This blinded, prospective, cross-sectional study involved 35 patients (60 hands) with clinically definite CTS and normal NCS, and 20 controls (40 hands). Cross-sectional area (CSAs) of the median nerve at the level of the pisiform bone and flexor retinaculum thickness (FRT) were measured. RESULTS: CSA was abnormal in 48.6% of patients (confidence interval 32.0-65.2%, P = 0.95). FRT was increased in only 34.3% (18.3-49.7%), but was independently abnormal in 2 patients. CSA abnormalities correlated with positive provocative tests and sensory loss. The HRUS changes were mild. CONCLUSIONS: HRUS confirms clinically diagnosed CTS in about half of the patients with normal NCS.
Assuntos
Síndrome do Túnel Carpal/diagnóstico por imagem , Mãos/diagnóstico por imagem , Nervo Mediano/diagnóstico por imagem , Condução Nervosa/fisiologia , Adulto , Estudos Transversais/métodos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Ultrassonografia , Adulto JovemRESUMO
A male patient developed ocular myasthenia gravis (MG) at the age of 33. He was anti-acetylcholine receptor antibody (anti-AChR Ab) negative. He received cholinesterase blocker for 5 months and went into a complete clinical remission that lasted untreated for 17 years. He relapsed recently with ocular symptoms only. He is now anti-AChR Ab positive and SFEMG is abnormal in a facial muscle. The patient is controlled with steroids. He had one of the longest spontaneous remissions reported in the natural history of MG, particularly unusual for an adult with the disease.