Meconium ileus in classical cystic fibrosis (Q97274): Difference between revisions

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Íleo meconial se refere à obstrução do íleo terminal por mecônio espesso; ocorre quase universalmente em neonatos com fibrose cística. Ó íleo meconial é quase sempre uma manifestação precoce da fibrose cística, que leva à produção de secreções gastrointestinais extremamente viscosas e aderentes à mucosa intestinal. Estas secreções são a manifestação de apresentação da fibrose cística em em 10 a 25% dos casos. A obstrução ocorre ao nível do íleo íleo terminal (diferentemente da obstrução colônica causada pela síndrome do tampão de mecônio) e pode ser diagnosticada pela ultrassonografia intestinal.
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Meconium ileus is obstruction of the terminal ileum by abnormally tenacious meconium; it almost universally occurs in neonates with cystic fibrosis. Meconium ileus is almost always an early manifestation of cystic fibrosis, which causes GI secretions to be extremely viscid and adherent to the intestinal mucosa. These secretions are the presenting manifestation of cystic fibrosis in 10 to 25% of cases. Obstruction occurs at the level of the terminal ileum (unlike the colonic obstruction caused by meconium plug syndrome) and may be diagnosed by prenatal ultrasonography.

Revision as of 13:22, 16 August 2026

Meconium ileus is obstruction of the terminal ileum by abnormally tenacious meconium; it almost universally occurs in neonates with cystic fibrosis. Meconium ileus is almost always an early manifestation of cystic fibrosis, which causes GI secretions to be extremely viscid and adherent to the intestinal mucosa. These secretions are the presenting manifestation of cystic fibrosis in 10 to 25% of cases. Obstruction occurs at the level of the terminal ileum (unlike the colonic obstruction caused by meconium plug syndrome) and may be diagnosed by prenatal ultrasonography.
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    Meconium ileus in classical cystic fibrosis
    Meconium ileus is obstruction of the terminal ileum by abnormally tenacious meconium; it almost universally occurs in neonates with cystic fibrosis. Meconium ileus is almost always an early manifestation of cystic fibrosis, which causes GI secretions to be extremely viscid and adherent to the intestinal mucosa. These secretions are the presenting manifestation of cystic fibrosis in 10 to 25% of cases. Obstruction occurs at the level of the terminal ileum (unlike the colonic obstruction caused by meconium plug syndrome) and may be diagnosed by prenatal ultrasonography.

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