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Ned Tijdschr Geneeskd ; 158: A7503, 2014.
Article in Dutch | MEDLINE | ID: mdl-25096033

ABSTRACT

BACKGROUND: Prader-Willi syndrome is characterised by hyperphagia and binge eating, without regurgitation. CASE DESCRIPTION: We present a 16-year-old girl with Prader-Willi syndrome exhibiting loss of appetite, stomach ache and regurgitation. Gastro-enteritis was suspected. However, she rapidly developed severe septic shock. During emergency surgery, a fully necrotic and ruptured stomach was seen. Despite respiratory, haemodynamic and surgical efforts, the patient died of necrotic intestinal bleeding. CONCLUSION: Binge eating or deviant gastric homeostasis could account for the relatively high incidence of gastric necrosis in patients with Prader-Willi syndrome. Loss of appetite and regurgitation in patients with this syndrome should be considered as warning signs of a possible life-threatening disorder.


Subject(s)
Prader-Willi Syndrome/complications , Stomach Diseases/pathology , Adolescent , Fatal Outcome , Female , Humans , Necrosis , Stomach Diseases/etiology
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