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1.
Pediatr Emerg Care ; 31(3): 207-8, 2015 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-25738240

RESUMEN

BACKGROUND: Unintentional acid ingestion is less commonly encountered than alkali ingestion. The injury develops for hours to days after ingestion and often results in progressively increasing difficulty in airway management. However, gastric perforation is rare. CASE: A 3-year-old boy presented to us with an orotonsillopharyngeal membrane and severe upper airway obstruction. Subsequently, he was diagnosed with a case of gastric perforation due to unintentional hydrochloric acid ingestion. He was treated with partial gastrectomy and feeding jejunostomy, and the recovery was good. CONCLUSIONS: Unintentional hydrochloric acid ingestion is rare in children. The manifestations masquerade many other clinical conditions, and the diagnosis is difficult in cases in which history of ingestion is not available. Treatment is symptomatic, and emergency surgery is indicated in case of gastrointestinal perforation.


Asunto(s)
Nutrición Enteral/métodos , Gastrectomía/métodos , Obstrucción de la Salida Gástrica/inducido químicamente , Ácido Clorhídrico/envenenamiento , Preescolar , Ingestión de Alimentos , Obstrucción de la Salida Gástrica/diagnóstico , Obstrucción de la Salida Gástrica/terapia , Humanos , Masculino , Tomografía Computarizada por Rayos X
2.
Indian J Hum Genet ; 19(1): 108-10, 2013 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-23901205

RESUMEN

Congenital absence of tibia is a rare anomaly, and may be total or partial, unilateral or bilateral. Total absence is more frequent than partial, unilateral absence occurs more often than bilateral, with right limb more commonly affected than the left. In partial defect, almost always the distal end of the bone is affected, and of the bilateral cases, there may be total absence on both sides, or total on one side and partial on the other. Males are slightly more commonly affected than the females. Though, the family history is usually negative for congenital abnormalities and other diseases, there is a considerable chance of occurrence of congenital defect of the tibia or of other abnormalities, in near or remote relatives. We report a case of newborn having bilateral tibial hemimelia type VIIa.

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