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

Base de dados
País/Região como assunto
Tipo de documento
País de afiliação
Intervalo de ano de publicação
1.
An Esp Pediatr ; 56(5): 466-71, 2002 May.
Artigo em Espanhol | MEDLINE | ID: mdl-12042123

RESUMO

Diencephalic syndrome (DS) is a complex of signs and symptoms related to hypothalamic dysfunction. Its main features are emaciation despite normal energy intake and an alert appearance. This syndrome has been described in association with space-occupying lesions of the hypothalamic-optic chiasm region, mainly low-grade glioma, and less often with tumors in the proximity of the IV ventricle. Two patients with DS are reported. The first patient was an 8-month old boy with classical features of DS. Extensive investigation of malabsorption revealed no abnormalities and the first neurologic sign was a rotatory nystagmus. Magnetic resonance imaging (MRI) showed evidence of a hypothalamic tumor, which was identified after surgical resection as a pilocytic astrocytoma. The second patient was an adolescent boy who presented a 20-kg weight loss over a 6-month period and psychological disturbances. Gastrointestinal disease was ruled out as a cause of malnutrition. Because of a polydipsia-polyuria syndrome, manifest while the patient was hospitalized with a suspected diagnosis of anorexia nervosa, MRI of the brain was performed. Multiple intracranial lesions were revealed, mainly in the hypothalamus, and were identified as a disseminated disgerminoma. No neurologic signs or symptoms were present. The patients died 2 years and 1 year after diagnosis, respectively. Although DS is rare, it should be considered in severe failure to thrive or emaciation despite adequate food intake and normal absorptive function of the small bowel.


Assuntos
Doenças Hipotalâmicas/complicações , Distúrbios Nutricionais/etiologia , Adolescente , Feminino , Humanos , Lactente , Masculino
2.
An Esp Pediatr ; 19(3): 184-92, 1983 Sep.
Artigo em Espanhol | MEDLINE | ID: mdl-6650993

RESUMO

Conditions at birth and evolution during the first year of life of a group of infants whose parents were affected by the Spanish Toxic Syndrome are presented. They are distributed in three groups: first those infants of high risk whose father or mother (or both) have consumed toxic oil; second children whose parents had consumed non-brandname oil not demonstrated to have been toxic and without signs of disease; and a third control group of normal newborns without previous medical history. From the present study, authors cannot affirm whether ingestion of toxic oil by pregnant women had influenced intrauterine growth or first year growth. Nonetheless, new studies are needed which clarify evolutionary aspects of these children.


Assuntos
Contaminação de Alimentos , Óleos/intoxicação , Óleos de Plantas , Efeitos Tardios da Exposição Pré-Natal , Doença Hepática Induzida por Substâncias e Drogas , Eosinofilia/induzido quimicamente , Ácidos Graxos Monoinsaturados , Feminino , Doenças Fetais/induzido quimicamente , Retardo do Crescimento Fetal/induzido quimicamente , Humanos , Lactente , Recém-Nascido , Masculino , Gravidez , Óleo de Brassica napus , Espanha
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA