Revision 53 for 'Celiac disease'

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Celiac disease

Celiac disease, also known as non-tropical sprue, is a T-cell mediated autoimmune chronic gluten intolerance condition characterized by a loss of villi in the proximal small bowel and gastrointestinal malabsorption (sprue).

It should always be considered as a possible underlying etiology in cases of iron deficiency anemia of uncertain cause.

Epidemiology

Celiac disease is relatively common in Caucasians, 1 in 200, but it is extremely rare in Asian and black people. There are two peaks of presentation, a small number of patients present early in childhood and the second, larger group of patients presents at 3rd and 4th decades. 

Clinical presentation

Many patients have a paucity of symptoms with no GI upset. However, abdominal pain is considered the most common symptom. Other manifestations include:

  • iron deficiency anemia and guaiac-positive stools
  • diarrhea
  • constipation
  • malabsorption, including fat-soluble vitamins
  • weight loss

Pathology

Celiac disease is a chronic autoimmune disease induced in genetically susceptible individuals after ingestion of gluten. Small bowel mucosa is primarily affected (submucosa, muscularis and serosa remain unaffected), resulting in progressive degrees of villous inflammation and destruction. The disease tends to start in the duodenum and extends into the ilium, resulting in induction crypt hyperplasia. Loss of villi, which absorb fluid, and hypertrophy of crypts, which produce fluid, result in a fluid excess in the small bowel lumen 8.  

The villous atrophy that occurs within the bowel also results in malabsorption of iron, folic acid, calcium and fat-soluble vitamins manifesting in a variety of signs, some of which may be non-specific.

The gold standard diagnostic test is a duodenal biopsy taken at endoscopy.

Histology
  • total villous loss, initially blunting, progressing to flattened mucosa
  • hyperplasia of the crypts 
  • epithelial infiltration with T-cell lymphocytes
Markers

Additionally, serum antibodies may be raised:

  • antitissue transglutaminase antibody (anti-tTG), IgA
  • deamidated gliadin peptide (DGP) antibodies, IgA
  • antiendomysial antibodies (EMA), IgA class
  • antireticulin antibodies (ARA), IgA class

Quantitative immunoglobulin A (IgA): measures the total level of IgA in the blood to determine if someone is deficient in the IgA class of antibodies. The IgG class of anti-tTG may be ordered for people who have a deficiency of IgA.

Associations

Radiographic features

Fluoroscopy

Features of small bowel barium studies are not sensitive enough for confident diagnosis, but the following changes may be seen:

CT

Features present on CT enteroclysis may include 3,6:

  • jejunoileal fold pattern reversal: thought to have the highest specificity is considered the most discriminating independent variable for the diagnosis of uncomplicated celiac disease
  • ileal fold thickening
  • vascular engorgement
  • prominent mesenteric lymph nodes may cavitate with a fluid-fat level
  • submucosal fat deposition in long-standing cases
  • other adjunctive features

Treatment and prognosis

A strict lifelong gluten-free diet (GFD) is the mainstay of treatment of this condition, and is effective in the vast majority of patients.

A small subset of patients do not respond despite fastidious gluten-free nutrition, refractory celiac disease 15.

Complications

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