Hirschsprung's disease: Difference between revisions
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Revision as of 17:44, 9 July 2016
Background
- Congenital aganglionosis of colon
- Usually rectosigmoid area
- Short segment affects rectum and small amount of distal colon
- Long segment affects more of colon, proximal intestine
- Rarely involves more proximal intestine
- Usually rectosigmoid area
- 30% associated with a syndrome
- 1:5,000 live births
Clinical Features
- Delayed meconium passage after birth
- 80% present within first month of life
- May have delayed presentation in milder disease
- Chronic constipation
- Encopresis
- Rectal prolapse
- Obstruction symptoms
- Neonatal toxic megacolon may occur
- Distended abdomen, bilious vomiting, enterocolitis
- Neonatal toxic megacolon may occur
- Enterocolitis
- Diarrhea, rectal bleeding, abdominal distention, fever
Differential Diagnosis
- Meconium ileus
- Cystic fibrosis
- Imperforate anus
- Constipation
- Bowel obstruction
Evaluation
- KUB distended colon, empty rectum
- Enterocolitis: distention, bowel wall thickening
- Obstruction: air fluid levels
- Diagnosis requires rectal biopsy (consult GI)
Management
- Consult pediatric surgeon for operative management
- Treat enterocolitis with broad spectrum antibiotics
Disposition
- Admit if symptoms of obstruction, enterocolitis