Eosinophilia
Mostrando 1-12 de 312 artigos, teses e dissertações.
-
1. Epidural morphine for chronic pain in a patient with peripheral neuropathy and DRESS syndrome. Case report
RESUMO JUSTIFICATIVA E OBJETIVOS: Neuropatia periférica é uma condição rara, de etiologia multifatorial. Dormência, parestesia, redução de força muscular e dor neuropática são sintomas comuns. O tratamento consiste em uso de anticonvulsivantes e antidepressivos. O objetivo deste estudo foi relatar o caso de dor crônica refratária a diversas tera
BrJP. Publicado em: 2022
-
2. SCHISTOSOMAL MYELORADICULOPATHY IN A NON-ENDEMIC AREA
RESUMO Objetivo: Relatar um caso de mielorradiculopatia esquistossomótica em área não endêmica. Descrição do caso: Paciente do sexo masculino, 11 anos, previamente hígido, com história aguda de paresia de membros inferiores, que evoluiu para membros superiores e tronco, associada à alteração de sensibilidade e formação de globo vesical. O exam
Rev. paul. pediatr.. Publicado em: 13/01/2020
-
3. Eosinophilic esophagitis-Where are we today?,
Resumo Objetivo: Fornecer uma visão geral do diagnóstico e do tratamento da esofagite eosinofílica na prática clínica e aumentar a visibilidade da doença entre os pediatras. Fontes dos dados: Foi feita uma busca na literatura relevante nos bancos de dados Medline, Embase, CINAHL e consensos e diretrizes recentes foram revisados. Síntese dos dados:
J. Pediatr. (Rio J.). Publicado em: 01/07/2019
-
4. Eosinophilic fasciitis: an atypical presentation of a rare disease
RESUMO A fasciite eosinofílica ou doença de Shulman é uma doença rara de etiologia desconhecida. É caracterizada por eosinofilia periférica, hipergamaglobulinemia e velocidade de sedimentação eritrocitária elevada. O diagnóstico é confirmado por biópsia profunda da pele. O tratamento de primeira linha é a corticoterapia. Apresentamos um caso rar
Rev. Assoc. Med. Bras.. Publicado em: 11/04/2019
-
5. Case for diagnosis. Erythroderma as manifestation of hypereosinophilic syndrome
Abstract: Hypereosinophilic syndrome is defined as persistent eosinophilia (>1500/µL for more than six months) associated with organ involvement, excluding secondary causes. It is a rare, potentially lethal disease that should be considered in cutaneous conditions associated with hypereosinophilia. We report a case of erythroderma as a manifestation of hype
An. Bras. Dermatol.. Publicado em: 2018-06
-
6. Gnathostomiasis: an emerging infectious disease relevant to all dermatologists
Abstract: Gnathostomiasis is a parasitic infection caused by the third larval stage of nematodes of the genus Gnathostoma. The disease is endemic in some countries around the world. In the American continent, the majority of cases is concentrated in Mexico, Ecuador, and Peru. However, due to increasing traveling either at the intercontinental or intracontine
An. Bras. Dermatol.. Publicado em: 2018-03
-
7. Prevalence of and risk factors for intestinal parasite infections in pediatric patients admitted to public hospitals in Southern Brazil
Abstract INTRODUCTION: This study aimed to evaluate the prevalence of intestinal parasitosis and to identify risk factors associated therewith in hospitalized children. METHODS: Three fecal samples from each patient were evaluated using three different techniques. The patients’ nutritional and socioeconomic status and hematologic profiles were evaluated.
Rev. Soc. Bras. Med. Trop.. Publicado em: 2017-12
-
8. Episodic angioedema associated with eosinophilia
Abstract: We report a 12-year-old girl who presented with recurrent angioedema on the face, trunk, and extremities, and concomitant marked weight gain for 5 years. During the episode, her white blood cell count increased to 47.7×109/L with 89.9% eosinophils, followed by elevated serum level of IL-5, IgE, IgM, and LDH. Histopathology showed perivascular eosi
An. Bras. Dermatol.. Publicado em: 2017-08
-
9. Angiolymphoid hyperplasia with eosinophilia versus Kimura's disease: a case report and a clinical and histopathological comparison
Abstract Angiolymphoid hyperplasia with eosinophilia is a rare and benign vascular tumor whose etiology remains uncertain. It clinically presents itself by angiomatous papules or nodules located on the head and neck. Many controversies in the literature are found in relation to angiolymphoid hyperplasia with eosinophilia and Kimura's disease - its main diffe
An. Bras. Dermatol.. Publicado em: 2017-06
-
10. Histopathological aspects of the liver of free-living and farmed bullfrogs (Lithobates catesbeianus)
ABSTRACT The objective of this study was to compare the histopathological aspects of the liver of free-living and farmed bullfrogs (Lithobates catesbeianus). Thirty liver samples were collected from young and adult bullfrogs in the states of Minas Gerais and Rio de Janeiro, Brazil. Marked blood congestion and even hemorrhage and a large number of melanomacro
R. Bras. Zootec.. Publicado em: 2017-04
-
11. Drug reaction with eosinophilia and systemic symptoms (DRESS) and its relation with autoimmunity in a reference center in Mexico
Abstract: BACKGROUND: Drug reaction with eosinophilia and systemic symptoms is a severe adverse drug reaction, with a reported mortality of 10%. Long-term outcomes involve organic failure and autoimmune diseases in some populations. OBJECTIVE: To evaluate the clinical prognosis of patients with drug reaction with eosinophilia and systemic symptoms. METHOD
An. Bras. Dermatol.. Publicado em: 2017-02
-
12. Cutaneous manifestations of Churg-Strauss syndrome: key to diagnosis
Abstract Churg-Strauss syndrome is a rare systemic vasculitis characterized by asthma and other allergy symptoms as well as eosinophilia and necrotizing vasculitis involving small and medium-sized vessels. Its prevalence in the general population ranges from 1-3 cases per million a year, varying according to the population studied. The authors describe a cas
An. Bras. Dermatol.. Publicado em: 2017