Late Diagnosis
Mostrando 25-36 de 380 artigos, teses e dissertações.
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25. Ultrasound Versus Contrast-Enhanced Magnetic Resonance Imaging for Subclinical Synovitis and Tenosynovitis: A Diagnostic Performance Study
OBJECTIVES: Radiographic manifestations of synovitis (e.g., erosions) can be observed only in the late stage of rheumatoid arthritis. Ultrasound is a noninvasive, cheap, and widely available technique that enables the evaluation of inflammatory changes in the peripheral joint. In the same way, dynamic contrast-enhanced magnetic resonance imaging (MRI) enabl
Clinics. Publicado em: 20/01/2020
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26. Rabies encephalitis and extra-neural manifestations in a patient bitten by a domestic cat
ABSTRACT Rabies encephalitis is a fatal zoonotic viral disease transmitted to humans either by domestic animals like dogs and cats or by wild animals like bats, skunks and raccoons. We present the case of a 25-year-old woman admitted due to behavioral disorders, generalized paresthesiasand acute respiratory deterioration compatible with a respiratory distres
Rev. Inst. Med. trop. S. Paulo. Publicado em: 17/01/2020
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27. Comparison of lupus patients with early and late onset nephritis: a study in 71 patients from a single referral center
Abstract Background: Nephritis occurs frequently in systemic lupus erythematosus (SLE) and may worsen disease morbidity and mortality. Knowing all characteristics of this manifestation helps to a prompt recognition and treatment. Aim: To compare the differences in clinical data, serological profile and treatment response of nephritis of early and late onse
Adv. rheumatol.. Publicado em: 13/01/2020
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28. Clinical and care profiles of children and adolescents with Sickle Cell Disease in the Brazilian Northeast region
Resumo Objetivos: descrever o perfil clínico-epidemiológico e assistencial dos pacientes pediátricos com doença falciforme. Métodos: estudo descritivo da totalidade (48) de crianças e adolescentes portadores de doença falciforme, atendidos em hospital de referência da rede pública da Paraíba. As informações obtidas em prontuários e entrevistas
Rev. Bras. Saude Mater. Infant.. Publicado em: 13/01/2020
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29. Case for diagnosis. Diffuse ulcerated nodular lesions
Abstract Langerhans cell histiocytosis is a rare clonal proliferative disease, characterized by the infiltration of one or multiple organs by histiocytes. Due to the diversity of signs and symptoms, the diagnosis of this disease is often late. The estimated incidence in adults is one to two cases per million, but the disease is probably underdiagnosed in thi
An. Bras. Dermatol.. Publicado em: 09/12/2019
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30. Visual loss as first clinical manifestation of X-linked adrenoleukodystrophy
Resumo A adrenoleucodistrofia ligada ao X (X-ALD) representa um grupo de doenças caracterizadas pelo acúmulo de ácidos graxos de cadeia muito longa (VLCFAs) nos tecidos. Suas manifestações clínicas costumam ser múltiplas. Alterações visuais podem estar presentes, contudo costumam surgir mais tardiamente na doença. Descrevemos aqui o caso de um meni
Rev. bras.oftalmol.. Publicado em: 02/12/2019
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31. Mortality in adolescents and young adults with chronic diseases during 16 years: a study in a Latin American tertiary hospital
RESUMO Objetivos: Avaliar a mortalidade entre adolescentes e pacientes adultos jovens com doenças crônicas acompanhados em um hospital terciário na América Latina. Métodos: Foi feito um estudo retrospectivo transversal em um hospital terciário/universitário no Estado de São Paulo, Brasil. Houve mortalidade de 529/2.850(18,5%) pacientes adolescentes
J. Pediatr. (Rio J.). Publicado em: 25/11/2019
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32. Clinical and anatomopathological aspects of patients with hantavirus cardiopulmonary syndrome in Uberaba, Minas Gerais, Brazil
ABSTRACT The hantavirus cardiopulmonary syndrome is considered an emerging disease in the Americas. Since 1993, thousands of cases have been reported from different countries, but mainly from Brazil. This study aims to describe some epidemiological, clinical and anatomopathological aspects of patients with hantavirus who presented poor outcome and were autop
Rev. Inst. Med. trop. S. Paulo. Publicado em: 10/10/2019
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33. Value of Contrast Transesophageal Echocardiography in the Detection of Intrapulmonary Vascular Dilatations in Hepatosplenic Schistosomiasis
Resumo Fundamento: A síndrome hepatopulmonar (SHP), presente em pacientes cirróticos, é pouco estudada na esquistossomose hepatoesplênica (EHE) e inclui a ocorrência de dilatações vasculares intrapulmonares (DVP). O ecocardiograma transesofágico com contraste (ETEc) de microbolhas é mais sensível que o ecocardiograma transtorácico com contraste (
Arq. Bras. Cardiol.. Publicado em: 03/10/2019
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34. Psychotic and affective symptoms of early-onset bipolar disorder: an observational study of patients in first manic episode
Objective: Presence of psychotic symptoms seems to be a commonplace in early-onset bipolar disorder (BD). However, few studies have examined their occurrence in adolescent-onset BD. We sought to investigate the frequency of affective and psychotic symptoms observed during the first manic episode in adolescents. Methods: Forty-nine adolescents with bipolar
Braz. J. Psychiatry. Publicado em: 26/09/2019
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35. How diseases became “genetic”
Resumo O presente artigo tem o objetivo de examinar as origens do termo “doença genética. No final do século XIX e início do XX, a vaga ideia que a doença manifesta entre familiares refletia uma “predisposição” familiar, foi substituída pela visão que essas doenças possuem causas específicas, enquanto a genética mendeliana forneceu as pista
Ciênc. saúde coletiva. Publicado em: 26/09/2019
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36. Left ventricular assessment in patients with mucopolysaccharidosis using conventional echocardiography and myocardial deformation by two-dimensional speckle-tracking method,
Resumo Objetivo: A mucopolissacaridose é uma doença genética rara, caracterizada por depósito intralisossômico de glicosaminoglicanos. O comprometimento cardiovascular é frequente. Sinais e sintomas cardíacos são subestimados pelo envolvimento da doença em outros órgãos. A terapia de reposição enzimática pode ser usada em mucopolissacaridose I
J. Pediatr. (Rio J.). Publicado em: 12/09/2019