Difference between revisions of "Colon"

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{{Main|CMV}}
{{Main|CMV}}
*Abbreviated ''CMV colitis''.
*Abbreviated ''CMV colitis''.
===General===
{{Main|Cytomegalovirus colitis}}
*Uncommon.
*Immunosuppressed population at risk, e.g. transplant recipients, individuals with [[HIV]].
 
===Microscopic===
Features:
*Enlarged nucleus - classically in endothelial cells.
 
DDx:
*[[Infectious colitis]] without a distinctive morphology.
*CMV colitis superimposed on [[inflammatory bowel disease]].
 
====Images====
<gallery>
Image:CMV_colitis_-_intermed_mag.jpg | CMV colitis - intermed. mag. (WC/Nephron)
Image:CMV_colitis_-_high_mag_-_cropped.jpg | CMV colitis - high mag. (WC/Nephron)
</gallery>
www:
*[http://www.flickr.com/photos/lunarcaustic/4615988256/ CMV colitis (flickr.com/lunar caustic)].
*[http://www.flickr.com/photos/lunarcaustic/4615988164/ CMV colitis (flickr.com/lunar caustic)]
===IHC===
*CMV +ve.
 
Others:
*HSV-1.
*HSV-2.
*VZV.
*[[EBV]].


==Intestinal spirochetosis==
==Intestinal spirochetosis==

Revision as of 22:47, 28 May 2015

Anatomy of the colon and rectum. (WC)

The colon is section of the large bowel. This article also covers the rectum and cecum as both have a similar mucosa.

It commonly comes to pathologists because there is a suspicion of colorectal cancer or a known history of inflammatory bowel disease (IBD).

An introduction to gastrointestinal pathology is found in the gastrointestinal pathology article. The anus and ileocecal valve are dealt with in separate articles.

Technically, the rectum and cecum are not part of the colon. Thus, inflammation of the rectum should be proctitis and inflammation of the cecum should be cecitis.

Common clinical problems

Obstruction

Top three (in adults):[1]

Bleeding

Mnemonic CHAND:[2]

Infectious colitis with bleeding - causes:

  • Enterohemorrhagic Escherichia coli (EHEC) -- commonly 0157:H7.
  • Campylobacter jejuni.
  • Clostridium difficile.
  • Shigella.

Infectious colitis in the immunosuppressed:

  • Cytomegalovirus (CMV).[3]
    • May afflict patients with IBD and lead to colectomy... as IBD patients are put on immunosuppression.[4]
    • Organ transplant recipients.
    • HIV/AIDS.

Images:

  • CMV colitis - high. mag. (WC/Nephron)

  • CMV colitis - intermed. mag. (WC/Nephron)

Grossing

Types of specimens

Introduction to colorectal surgery:

  1. Colonic resection - remove a piece of large bowel.
  2. Total colectomy - leaves rectum and anus.[5]
  3. Subtotal colectomy - part of colon removed --or-- some of the rectum remains.
  4. Right hemicolectomy - right colon + distal ileum.
  5. Lower anterior resection (LAR) - proximal rectum +/- sigmoid (for proximal rectal malignancies).
  6. Abdominoperineal resection (APR) - anus + rectum - results in a permanent stoma (for distal rectal malignancies).
  7. Stoma - these are often done emergently and then get cut-out after the patient's condition has settled.
  8. Doughnuts (also donuts) from an end-to-end anastomosis stapler.
    • Often accompany lower anterior resections.

Images

  • APR specimen - anterior (WC)

  • APR specimen - lateral (WC)

  • APR specimen - inked (WC)

Identifying the specimen

  • Transverse colon - has omentum.
  • Ascending colon - usu. comes with ileocecal valve and a bit of ileum.
  • Descending colon - has a bare area.
  • Rectum - has adventitia.
    • Pathologists define it as starting where the adventitia starts/the serosal surface no longer completely surrounds the large intestine.[7]
    • Anatomists define it in relation to the third sacral vertebra.[8]

Images

  • Sigmoid and rectum. APR specimen. (WC)

Lymph nodes

Quirke method

  • Bowel is not opened - it is fixed... then sliced.[10][11]

Standard method

  • Bowel is prep'ed by opening it along the antimesenteric side.
  • Dimensions - length, circumference at both margins.
  • Radial margin/circumferential margin - should be painted.
    • Rectum starts/sigmoid ends @ place where serosa ends on the posterior aspect of the bowel.
      • The proximal, anterior aspect of the rectum has serosa, i.e. it is not painted.

Common non-neoplastic disease

Colorectal polyps

Main article: Intestinal polyps

Polyps are the bread & butter of GI pathology. They are very common.

Main types:

  • Hyperplastic - most common, benign.
  • Adenomatous - quite common, pre-malignant.
  • Hamartomatous - rare, weird & wonderful.
  • Inflammatory, AKA inflammatory pseudopolyps - associated with IBD.

Most common (images):

  • Hyperplastic polyp image - intermed. mag. (WC/Nephron)

  • Hyperplastic polyp image - low mag. (WC/Nephron)

Ischemic colitis

  • AKA colonic ischemia.
  • AKA ischemia of the colon.
Main article: Ischemic colitis

Diverticular disease

Main article: Diverticular disease

Pseudomembranous colitis

Main article: Pseudomembranous colitis

Volvulus

Main article: Volvulus

Inflammatory diseases

Inflammatory bowel disease

Main article: Inflammatory bowel disease

The bread 'n butter of gastroenterology. A detailed discussion of IBD is in the inflammatory bowel disease article. It comes in two main flavours (Crohn's disease, ulcerative colitis).

Microscopic

Features helpful for the diagnosis of IBD - as based on a study:[12]

  • Basal, i.e. crypt base, plasmacytosis with severe chronic inflammation,
  • Crypt architectural abnormalities, and
  • Distal Paneth cell metaplasia.
    • Paneth cells should not be in the left colon[13] - if you see 'em think of IBD and other long-standing injurious processes.
    • Some claim that (friendly right colonic) paneth cells and paneth cell metaplasia look quite different and can be distinguished.[14]

Microscopic colitis

Microscopic colitis may refer to a microscopic manifestation of an unspecified disease process that can be apparent macroscopically. This section links to a pair of diseases (lymphocytic colitis and collagenous colitis) that are considered to only have microscopic manifestations and characteristic clinical presentation.
Main article: Lymphocytic colitis
Main article: Collagenous colitis

Diversion colitis

Main article: Diversion colitis

Eosinophilic colitis

  • Abbreviated EC.
Main article: Eosinophilic colitis

Infectious

Infectious colitis

This section covers non-specific colitides that appear to have an infective etiology.

General

  • Common.
  • Diarrhea - typical symptom.

Gross

  • +/-Erythema on endoscopy.

Microscopic

Features:

  • Neutrophils predominant - key feature.[15]
    • The neutrophils are often superficial - they go to were the bad guys are.
  • No architectural distortion - if acute.

DDx:

IHC

Done if the patient is immunosuppressed, or there is clinical or morphological suspicion:

Sign out

ASCENDING COLON, BIOPSY:
- MILD ACTIVE COLITIS, SEE COMMENT.

COMMENT:
There is are no granulomas.  The crypt architecture is normal.  A benign lymphoid nodule is
present.

The differential diagnosis includes infective etiologies, early inflammatory
bowel disease and ischemia.  The histomorphology is more in keeping with an infective
etiology as neutrophils are a predominant feature; however, clinical correlation is
required.

Cytomegalovirus colitis

Main article: CMV
  • Abbreviated CMV colitis.
Main article: Cytomegalovirus colitis

Intestinal spirochetosis

  • AKA intestinal spirochetes; more specifically colonic spirochetes, colonic spirochetosis.
Main article: Intestinal spirochetosis

Amebiasis

  • May also be spelled amoebiasis.
Main article: Amebiasis

Cryptosporidiosis

Main article: Cryptosporidiosis

General

  • Usually in immune incompetent individuals, e.g. HIV/AIDS.

Microscopic

Features:

  • Uniform spherical nodules 2-4 micrometres in diameter, typical location - GI tract brush border.
    • Bluish staining of brush border key feature - low power.

Rectal pathology

Solitary rectal ulcer

  • AKA solitary ulcer syndrome of the rectum, abbreviated SUS.
  • AKA solitary rectal ulcer syndrome.
  • Mucosal prolapse syndrome may be used as a synonym; however, it encompasses other entities.[17]

General

  • Clinically may be suspected to a malignancy - biopsied routinely.
  • Mucosal ulceration.
  • "Three-lies disease":[18]
  1. May not be solitary.
  2. May not be rectal -- can be in left colon.
  3. May not be ulcerating -- non-ulcerated lesions: polypoid and/or erythematous.

Note: Each of the words in solitary rectal ulcer is a lie.

Epidemiology

  • Typically younger patients - average age of presentation ~30 years in one study.[19]
  • Rare.

Clinical presentation

  • Usually presents as BRBPR ~ 85% of cases.[19]
  • Abdominal pain present in approx. 1/3.[19]
    • May be very painful.

Treatment:

  • Usually conservative, i.e. non-surgical.
  • Resection - may be done for fear of malignancy.

Gross

  • Classically, anterior or anterolateral wall of the rectum.[18]

Microscopic

Features:[18][20]

  • Fibrosis of the lamina propria.
  • Thickened muscularis mucosa with abnormal extension to the lumen.
  • +/-Mucosa ulceration.
  • +/-Submucosal fibrosis.

DDx:

IHC

  • p53 -ve.
    • May be used to help exclude adenocarcinoma.

Rectal prolapse

Main article: Rectal prolapse

Neoplastic disease

Colorectal Tumours

Main article: Colorectal tumours

These are very common. The are covered in a separate article entitled colorectal tumours.

Neuroendocrine tumour

Main article: Neuroendocrine neoplasms#GI tract

Goblet cell carcinoid

Described in detail in the appendix article.
  • AKA crypt cell carcinoma.
  • Biphasic tumour; features of carcinoid tumour and adenocarcinoma.

Other

Colonic pseudo-obstruction

Main article: Colonic pseudo-obstruction

Pseudomelanosis coli

  • AKA melanosis coli.
Main article: Pseudomelanosis coli

Angiodysplasia

General

  • Causes (lower) GI haemorrhage.
  • Generally, not a problem pathologists see.
  • May be associated with aortic stenosis; known as Heyde syndrome.[21]

Epidemiology:

  • Older people.

Etiology:

  • Thought to be caused by the higher wall tension of cecum (due to larger diameter) and result from (intermittent) venous occlusion/focal dilation of vessels.[22]

Gross

  • Cecum - classic location.

Note:

Microscopic

Features:[23]

  • Dilated vessels in mucosa and submucosa.

Drugs

Main article: Drug toxicity

Sodium polystyrene sulfonate

  • AKA Kayexalate.

General

  • Used to treat hyperkalemia - as may be seen in renal failure.

Microscopic

Features:[24]

Image

  • Adenocarcinoma and sodium polystyrene crystals (WC/Nephron)

Graft-versus host disease

Main article: Graft-versus-host disease
  • Abbreviated as GVHD.
  • Seen in the context of bone marrow transplants.

Bowel transplant

The histology of bowel transplant rejection is identical to GVHD - see GVHD.

Chronic constipation

This section deals with chronic constipation that has no apparent cause.

General

General differential diagnosis for constipation:

Gross

  • No changes.

Microscopic

Features:

  • Colon within normal limits.
    • Look for the Ganglion cells (submucosal plexus, myenteric plexus).
    • Look for interstitial cells of Cajal (with CD117) - typically most common around the myenteric plexus.[26]

Negatives:

  • No significant vascular disease.
  • No fibrosis.
  • No loss of muscle.

Stains & IHC

Work-up if no tumour is identified:[27][28]

  • Routine H&E.
  • Smooth muscle actin - confirm myocyte loss.
  • Gomori trichrome - examine connective tissue.
  • CD117 - to look for the interstitial cells of Cajal.
    • <50% the expected = abnormal.[28]
      • Normal numbers not defined.
  • HU - neuronal marker.[29]

Sign out

  • A long list of things to report is contained the recommendation of a working group.[28]
    • Most pathology practises do not report much.
TERMINAL ILEUM, CECUM, COLON (ASCENDING, TRANSVERSE AND SIGMOID), COLECTOMY:
- SMALL BOWEL, CECUM, AND COLON WITHIN NORMAL LIMITS.
- FOUR LYMPH NODES NEGATIVE FOR MALIGNANCY ( 0 POSITIVE / 4 ).
- NEGATIVE FOR DYSPLASIA AND NEGATIVE FOR MALIGNANCY.

COMMENT:
Several stains were done:
 CD117: interstitial cells of Cajal present, no apparent decrease.
 SMA: no significant myocyte loss.
 Gomori trichrome: no abnormal fibrosis apparent.
 Tau: no abnormalities apparent.

See also

References

  1. ↑ URL: http://www.emedicine.com/EMERG/topic65.htm. Accessed on: 28 June 2011.
  2. ↑ TN 2007 G29.
  3. ↑ Golden MP, Hammer SM, Wanke CA, Albrecht MA (September 1994). "Cytomegalovirus vasculitis. Case reports and review of the literature". Medicine (Baltimore) 73 (5): 246–55. PMID 7934809.
  4. ↑ Kandiel A, Lashner B (December 2006). "Cytomegalovirus colitis complicating inflammatory bowel disease". Am. J. Gastroenterol. 101 (12): 2857–65. doi:10.1111/j.1572-0241.2006.00869.x. PMID 17026558.
  5. ↑ http://www.allaboutbowelsurgery.com/shared/stoma_care/stoma_surgery/procedures/surgery_colon/subtotal.htm
  6. ↑ Arbman, G.; Nilsson, E.; Hallböök, O.; Sjödahl, R. (Mar 1996). "Local recurrence following total mesorectal excision for rectal cancer.". Br J Surg 83 (3): 375-9. PMID 8665198.
  7. ↑ Lester, Susan Carole (2010). Manual of Surgical Pathology (3rd ed.). Saunders. pp. 339. ISBN 978-0-323-06516-0.
  8. ↑ URL: http://www.bartleby.com/107/249.html. Accessed on: 19 October 2012.
  9. ↑ Bilimoria KY, Bentrem DJ, Stewart AK, et al. (September 2008). "Lymph node evaluation as a colon cancer quality measure: a national hospital report card". J. Natl. Cancer Inst. 100 (18): 1310–7. doi:10.1093/jnci/djn293. PMID 18780863. http://www.medscape.com/viewarticle/581463.
  10. ↑ West NP, Morris EJ, Rotimi O, Cairns A, Finan PJ, Quirke P (September 2008). "Pathology grading of colon cancer surgical resection and its association with survival: a retrospective observational study". Lancet Oncol. 9 (9): 857–65. doi:10.1016/S1470-2045(08)70181-5. PMID 18667357.
  11. ↑ West NP, Finan PJ, Anderin C, Lindholm J, Holm T, Quirke P (July 2008). "Evidence of the oncologic superiority of cylindrical abdominoperineal excision for low rectal cancer". J. Clin. Oncol. 26 (21): 3517–22. doi:10.1200/JCO.2007.14.5961. PMID 18541901.
  12. ↑ Tanaka M, Riddell RH, Saito H, Soma Y, Hidaka H, Kudo H (January 1999). "Morphologic criteria applicable to biopsy specimens for effective distinction of inflammatory bowel disease from other forms of colitis and of Crohn's disease from ulcerative colitis". Scand. J. Gastroenterol. 34 (1): 55–67. PMID 10048734.
  13. ↑ Tanaka M, Saito H, Kusumi T, et al (December 2001). "Spatial distribution and histogenesis of colorectal Paneth cell metaplasia in idiopathic inflammatory bowel disease". J. Gastroenterol. Hepatol. 16 (12): 1353–9. PMID 11851832. http://www3.interscience.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0815-9319&date=2001&volume=16&issue=12&spage=1353.
  14. ↑ Rubio CA, Nesi G (2003). "A simple method to demonstrate normal and metaplastic Paneth cells in tissue sections". In Vivo 17 (1): 67–71. PMID 12655793.
  15. ↑ 15.0 15.1 Iacobuzio-Donahue, Christine A.; Montgomery, Elizabeth A. (2005). Gastrointestinal and Liver Pathology: A Volume in the Foundations in Diagnostic Pathology Series (1st ed.). Churchill Livingstone. pp. 324. ISBN 978-0443066573.
  16. ↑ Karlitz, JJ.; Li, ST.; Holman, RP.; Rice, MC. (Jan 2011). "EBV-associated colitis mimicking IBD in an immunocompetent individual.". Nat Rev Gastroenterol Hepatol 8 (1): 50-4. doi:10.1038/nrgastro.2010.192. PMID 21119609.
  17. ↑ Abid, S.; Khawaja, A.; Bhimani, SA.; Ahmad, Z.; Hamid, S.; Jafri, W. (2012). "The clinical, endoscopic and histological spectrum of the solitary rectal ulcer syndrome: a single-center experience of 116 cases.". BMC Gastroenterol 12: 72. doi:10.1186/1471-230X-12-72. PMID 22697798.
  18. ↑ 18.0 18.1 18.2 Crespo Pérez L, Moreira Vicente V, Redondo Verge C, López San Román A, Milicua Salamero JM (November 2007). "["The three-lies disease": solitary rectal ulcer syndrome"] (in Spanish; Castilian). Rev Esp Enferm Dig 99 (11): 663–6. PMID 18271667. http://www.grupoaran.com/mrmUpdate/lecturaPDFfromXML.asp?IdArt=459864&TO=RVN&Eng=1.
  19. ↑ 19.0 19.1 19.2 Chong VH, Jalihal A (December 2006). "Solitary rectal ulcer syndrome: characteristics, outcomes and predictive profiles for persistent bleeding per rectum". Singapore Med J 47 (12): 1063–8. PMID 17139403. http://www.sma.org.sg/smj/4712/4712a7.pdf.
  20. ↑ Malik, AK.; Bhaskar, KV.; Kochhar, R.; Bhasin, DK.; Singh, K.; Mehta, SK.; Datta, BN. (Jul 1990). "Solitary ulcer syndrome of the rectum--a histopathologic characterisation of 33 biopsies.". Indian J Pathol Microbiol 33 (3): 216-20. PMID 2091997.
  21. ↑ Hui YT, Lam WM, Fong NM, Yuen PK, Lam JT (August 2009). "Heyde's syndrome: diagnosis and management by the novel single-balloon enteroscopy". Hong Kong Med J 15 (4): 301–3. PMID 19652242. http://www.hkmj.org/abstracts/v15n4/301.htm.
  22. ↑ 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. 854. ISBN 0-7216-0187-1.
  23. ↑ 23.0 23.1 Hemingway, AP. (Apr 1988). "Angiodysplasia: current concepts.". Postgrad Med J 64 (750): 259-63. PMID 3054852.
  24. ↑ Abraham SC, Bhagavan BS, Lee LA, Rashid A, Wu TT (May 2001). "Upper gastrointestinal tract injury in patients receiving kayexalate (sodium polystyrene sulfonate) in sorbitol: clinical, endoscopic, and histopathologic findings". Am. J. Surg. Pathol. 25 (5): 637-44. PMID 11342776. http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0147-5185&volume=25&issue=5&spage=637.
  25. ↑ 25.0 25.1 25.2 Knowles, CH.; Farrugia, G. (Feb 2011). "Gastrointestinal neuromuscular pathology in chronic constipation.". Best Pract Res Clin Gastroenterol 25 (1): 43-57. doi:10.1016/j.bpg.2010.12.001. PMID 21382578.
  26. ↑ Streutker, CJ.; Huizinga, JD.; Driman, DK.; Riddell, RH. (Jan 2007). "Interstitial cells of Cajal in health and disease. Part I: normal ICC structure and function with associated motility disorders.". Histopathology 50 (2): 176-89. doi:10.1111/j.1365-2559.2006.02493.x. PMID 17222246. http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2559.2006.02493.x/pdf.
  27. ↑ IAV. 15 December 2009.
  28. ↑ 28.0 28.1 28.2 Knowles, CH.; De Giorgio, R.; Kapur, RP.; Bruder, E.; Farrugia, G.; Geboes, K.; Gershon, MD.; Hutson, J. et al. (Aug 2009). "Gastrointestinal neuromuscular pathology: guidelines for histological techniques and reporting on behalf of the Gastro 2009 International Working Group.". Acta Neuropathol 118 (2): 271-301. doi:10.1007/s00401-009-0527-y. PMID 19360428.
  29. ↑ Barami K, Iversen K, Furneaux H, Goldman SA (September 1995). "Hu protein as an early marker of neuronal phenotypic differentiation by subependymal zone cells of the adult songbird forebrain". J. Neurobiol. 28 (1): 82–101. doi:10.1002/neu.480280108. PMID 8586967.
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