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خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : 3 مورد
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Causes of chronic diarrhea in neonates and young infants

Causes of chronic diarrhea in neonates and young infants
Disorder Clinical clues or characteristics Evaluation
Dietary triggers
Food protein-induced proctocolitis Colitis in otherwise healthy infant; usually caused by cow's milk protein in breast milk or formula. Trial of cow's milk-free diet
Food protein-induced enterocolitis syndrome Diarrhea, vomiting, and vital sign instability immediately following intake of inciting foods. Allergy evaluation, dietary restrictions
Infectious
Rotavirus, norovirus, cytomegalovirus, enteropathogenic bacteria Sick contacts, watery or bloody diarrhea. Stool culture, PCR
Postinfectious diarrhea History of recent acute diarrhea, with ongoing malabsorptive symptoms. Trial of lactose-free diet
Associated with medical illness
Necrotizing enterocolitis Prematurity or underlying medical illness. Presents with feeding intolerance, temperature instability, abdominal distention. Pneumatosis intestinalis on plain radiograph. Abdominal radiograph
Short bowel syndrome Usually due to resection of substantial portions of bowel (eg, because of necrotizing enterocolitis or atresias). Occasionally due to loss of a specific absorptive site (eg, bile acid malabsorption after resection of the terminal ileum). History of intestinal resection
Anatomic defects
Malrotation with intermittent volvulus Typically presents with obstructive symptoms and vomiting, but occasionally presents with diarrhea, which may be bloody, and intermittent abdominal pain. Abdominal radiograph, fluoroscopic UGI/SBFT
Hirschsprung disease Typically presents with constipation and signs of distal obstruction, but occasionally presents with Hirschsprung-associated enterocolitis, a potentially life-threatening illness with a sepsis-like picture including diarrhea or subacute diarrhea with poor weight gain. Hirschsprung disease is particularly common in infants with Down syndrome. Barium enema, rectal biopsy
Congenital intestinal pseudo-obstruction Impaired intestinal motility without anatomic obstruction, leading to diffuse bowel dilation, abdominal distension, often vomiting and constipation, and sometimes diarrhea. Contrast radiographs often reveal very dilated bowel loops and malrotation (similar to congenital short bowel syndrome). Fluoroscopic UGI/SBFT
Congenital short bowel syndrome Generalized malabsorptive diarrhea and dilated bowel loops despite lack of abdominal distension, often with bile-stained vomiting and failure to thrive. Contrast radiographs often reveal malrotation (similar to congenital intestinal pseudo-obstruction). Fluoroscopic UGI/SBFT
Congenital diarrheas and enteropathies (CODEs)
Many types; main categories are:
  • Disorders of epithelial nutrient transport
  • Disorders of electrolyte transport
  • Disorders of epithelial enzymes and metabolism
  • Disorders of epithelial trafficking and polarity
  • Enteroendocrine cell development dysfunction
  • Immune dysregulation-associated enteropathies

CODEs are rare genetic disorders that cause malabsorption or other intestinal dysfunction.

A CODE is more likely if diarrhea:
  • Presents in the neonatal period
  • Requires critical care intervention (eg, for dehydration)
  • There is history of polyhydramnios or consanguinity
  • There is multisystem involvement (eg dysmorphism or other congenital anomalies, or signs/symptoms of immunodeficiency)
Refer to UpToDate content and algorithm
PCR: polymerase chain reaction; UGI/SBFT: upper gastrointestinal series with small bowel follow-through; CODEs: congenital diarrheas and enteropathies.
Graphic 118302 Version 3.0

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