Difference between revisions of "Celiac sprue"

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'''Celiac sprue''' is a common pathology that affects the [[duodenum]].  
'''Celiac sprue''', also '''celiac disease''', is a common pathology that affects the [[duodenum]].  


An introduction to gastrointestinal pathology is in the ''[[gastrointestinal pathology]]'' article.  It covers basic gastrointestinal histology.
An introduction to gastrointestinal pathology is in the ''[[gastrointestinal pathology]]'' article.  It covers basic gastrointestinal histology.
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Most pathologists do not grade celiac sprue.
Most pathologists do not grade celiac sprue.


The most common system is the ''modified Marsh system'':<ref>{{cite journal |author=Oberhuber G, Granditsch G, Vogelsang H |title=The histopathology of coeliac disease: time for a standardized report scheme for pathologists |journal=Eur J Gastroenterol Hepatol |volume=11 |issue=10 |pages=1185–94 |year=1999 |month=October |pmid=10524652 |doi= |url=}}</ref><ref name=pmid12145668>{{cite journal |author=Wahab PJ, Meijer JW, Dumitra D, Goerres MS, Mulder CJ |title=Coeliac disease: more than villous atrophy |journal=Rom J Gastroenterol |volume=11 |issue=2 |pages=121–7 |year=2002 |month=June |pmid=12145668 |doi= |url=}}</ref>
The most common system is the ''Marsh system'' (abbreviated):<ref>{{cite journal |author=Oberhuber G, Granditsch G, Vogelsang H |title=The histopathology of coeliac disease: time for a standardized report scheme for pathologists |journal=Eur J Gastroenterol Hepatol |volume=11 |issue=10 |pages=1185–94 |year=1999 |month=October |pmid=10524652 |doi= |url=}}</ref><ref name=pmid12145668>{{cite journal |author=Wahab PJ, Meijer JW, Dumitra D, Goerres MS, Mulder CJ |title=Coeliac disease: more than villous atrophy |journal=Rom J Gastroenterol |volume=11 |issue=2 |pages=121–7 |year=2002 |month=June |pmid=12145668 |doi= |url=}}</ref>
{| class="wikitable"
{| class="wikitable"
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| Blunted villi
| Blunted villi
| Flattened mucosa
| Flattened mucosa
|}
The ''Marsh system'' (full):<ref>{{cite journal |author=Oberhuber G, Granditsch G, Vogelsang H |title=The histopathology of coeliac disease: time for a standardized report scheme for pathologists |journal=Eur J Gastroenterol Hepatol |volume=11 |issue=10 |pages=1185–94 |year=1999 |month=October |pmid=10524652 |doi= |url=}}</ref>
{| class="wikitable"
| Marsh score
| Descriptors
| Alternate descriptors
| Crypts
| IEL
|-
| Marsh 0
| Well-formed villi
| Normal villous arch.
|
|
|-
| Marsh 1
| Well-formed villi
| Normal villous arch.
|
|
|-
| March 2
| Well-formed villi
| Normal villous arch.
|
|
|-
| Marsh 3A
| Partial villous atrophy
| Blunted villi
|
|
|-
| Marsh 3B
| Partial villous atrophy
| Blunted villi
|
|
|-
| Marsh 3C
| Total villous atrophy
| Flattened mucosa
|
|
|}
|}



Revision as of 15:32, 7 February 2011

Celiac sprue, also celiac disease, is a common pathology that affects the duodenum.

An introduction to gastrointestinal pathology is in the gastrointestinal pathology article. It covers basic gastrointestinal histology.

Etiology

  • Autoimmune.

Epidemiology

Variants of celiac sprue

  1. Latent celiac sprue.
    • ONLY intraepithelial lymphocytes.
    • NO villous arch. change.
  2. Refractory celiac sprue.
    • Subclassified - see microscopic.
  3. Collagenous sprue.
    • Abundant mucosal collagen - see microscopic.

Clinical

Treatment

  • Gluten free diet.
    • Mnemonic: BROW = barley, rye, oats, wheat.

Serologic testing

  • Anti-transglutaminase antibody.
    • Alternative test: anti-endomysial antibody.
  • IgA -- assoc. with celiac sprue.

Microscopic

Features:[3]

  • Intraepithelial lymphocytes - key feature.
    • Should be more pronounced at tips of villi.[4]
  • Loss of villi - important feature.
    • Normal duodenal biopsy should have 3 good villi.
  • Plasma cells - abundant (weak feature).
  • Macrophages.
  • Mitosis increased (in the crypts).
  • +/-Collagen band (pink material in mucosa) - "Collagenous sprue"; must encompass ~25% of mucosa.

Image:

Notes:

  • If you see acute inflammatory cells, i.e. neutrophils, consider Giardiasis and other infectious etiologies.
  • Biopsy should consist of 2-3 sites. In children it is important to sample the duodenal cap, as it is the only affected site in ~10% of cases.
  • Flat lesions without IELs are unlikely to be celiac sprue.
  • Mucosa erosions are rare in celiac sprue; should prompt consideration of an alternate diagnosis (infection, medications, Crohn's disease).

Refractory sprue

  • Type I: CD3 ~= CD8.
  • Type II: CD3 20% + less than CD8.

Grading

Most pathologists do not grade celiac sprue.

The most common system is the Marsh system (abbreviated):[5][6]

Marsh 1 Marsh 3A Marsh 3C
Descriptors Well-formed villi Partial villous atrophy Total villous atrophy
Alternate descriptors Normal villous arch. Blunted villi Flattened mucosa

The Marsh system (full):[7]

Marsh score Descriptors Alternate descriptors Crypts IEL
Marsh 0 Well-formed villi Normal villous arch.
Marsh 1 Well-formed villi Normal villous arch.
March 2 Well-formed villi Normal villous arch.
Marsh 3A Partial villous atrophy Blunted villi
Marsh 3B Partial villous atrophy Blunted villi
Marsh 3C Total villous atrophy Flattened mucosa

Notes:

  • Villous atrophy can be assessed endoscopically.[8]

DDx

  • Giardiasis.
    • Have giarrdia organisms.
    • Always consider Giardiasis and especially on exams.
  • Whipple's disease (very rare).
    • Abundant macrophages should make one suspicious.

See also

References

  1. TN 2007 D22
  2. Kumar, V.; Jarzabek-Chorzelska, M.; Sulej, J.; Karnewska, K.; Farrell, T.; Jablonska, S. (Nov 2002). "Celiac disease and immunoglobulin a deficiency: how effective are the serological methods of diagnosis?". Clin Diagn Lab Immunol 9 (6): 1295-300. PMID 12414763.
  3. Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic basis of disease (7th ed.). St. Louis, Mo: Elsevier Saunders. pp. 843. ISBN 0-7216-0187-1.
  4. Biagi F, Luinetti O, Campanella J, et al. (August 2004). "Intraepithelial lymphocytes in the villous tip: do they indicate potential coeliac disease?". J. Clin. Pathol. 57 (8): 835–9. doi:10.1136/jcp.2003.013607. PMC 1770380. PMID 15280404. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1770380/.
  5. Oberhuber G, Granditsch G, Vogelsang H (October 1999). "The histopathology of coeliac disease: time for a standardized report scheme for pathologists". Eur J Gastroenterol Hepatol 11 (10): 1185–94. PMID 10524652.
  6. Wahab PJ, Meijer JW, Dumitra D, Goerres MS, Mulder CJ (June 2002). "Coeliac disease: more than villous atrophy". Rom J Gastroenterol 11 (2): 121–7. PMID 12145668.
  7. Oberhuber G, Granditsch G, Vogelsang H (October 1999). "The histopathology of coeliac disease: time for a standardized report scheme for pathologists". Eur J Gastroenterol Hepatol 11 (10): 1185–94. PMID 10524652.
  8. Ciaccio EJ, Bhagat G, Tennyson CA, Lewis SK, Hernandez L, Green PH (September 2010). "Quantitative Assessment of Endoscopic Images for Degree of Villous Atrophy in Celiac Disease". Dig Dis Sci. doi:10.1007/s10620-010-1371-6. PMID 20844959.

External links

Review article(s)