Inflammatory bowel disease
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Inflammatory bowel disease, abbreviated IBD, is the bread 'n butter of gastroenterology, and a significant number of gastrointestinal pathology specimens.
It exists in two main flavours:
- Crohn's disease (CD).
- Ulcerative colitis (UC).
Both are associated with an increased risk of colorectal carcinoma.[1]
Clinical
- It is important to differentiate UC and CD as the management is different.
- UC patients get pouches... CD patients do not.
- It is said that: There 's nothing like a pouch to bring out Crohn's disease.[2]
- People with long standing IBD have an increased risk for:
- Carcinoma - usually colorectal carcinoma.[3]
- Small increased risk for small bowel adenocarcinoma in Crohn's disease.[3]
- Lymphoma - in association with thiopurine use.[4]
- Carcinoma - usually colorectal carcinoma.[3]
Extra-intestinal manifestations of inflammatory bowel disease
Mnemonic (family-rated version) excellent cardiac surgery is pleasant and appreciated:
- Erythema nodosum.
- Clubbing.
- Sclerosing cholangitis.
- Iritis.
- Pyoderma gangrenosum.
- Aphthous ulcers.
- Arthritis.
Molecular
- NOD2[5] (AKA CARD15) variants are associated with stricturing CD, early need for surgery and recurrence.[6]
General clinical differential diagnosis
- Crohn's disease.
- Ulcerative colitis.
- Infective colitis/enteritis.
- Ischemic colitis/enteritis.
- Radiation colitis.
Others:
Specimens
- Biopsies for diagnosis.
- Surveillance biopsies - to rule-out dysplasia.
- Resections of disease that has failed medical management.
- Resections for dysplasia associated with inflammatory bowel disease.
Note:
- Surveillance biopsies and biopsies for diagnosis should specify the site.
- Slight gradients exists in the large bowel that can be exploited for diagnostic purposes if the site information is known, for example:
- Paneth cell distal to the splenic flexure are abnormal.
- Ulcerative colitis is often more severe distally - even in a pancolitis, as the disease starts in the rectum and progresses toward the cecum.
- Slight gradients exists in the large bowel that can be exploited for diagnostic purposes if the site information is known, for example:
Spanking the clinician for submitting it all in one bottle
COLON (SITE NOT FURTHER SPECIFIED), BIOPSIES: - MODERATE CHRONIC ACTIVE COLITIS. - FOCALLY ABUNDANT EOSINOPHILS. - NEGATIVE FOR DYSPLASIA. - PLEASE SEE COMMENT. COMMENT: The sections show colorectal-type mucosa with focal cryptitis and rare neutrophilic crypt abscesses. There are up to 80 eosinophils per high power field (HPF), where one HPF is ~0.2376 mm*mm. No eosinophilic crypt abscesses are identified. Paneth cells are present focally; however, the significance of the paneth cells cannot determined as the biopsy sites are not known. Mild architectural changes, suggestive of a chronic colitis, are present. No granulomas are identified. Lymphoid aggregates with germinal centre formation are present in multiple fragments. The lamina propria has abundant plasma cells throughout the fragments; no fragments have apparent relative sparing. It is not possible to assess whether there is a mild gradient of less severe to more severe architectural changes from proximal to distal large bowel, as may be seen in individuals with ulcerative colitis. The findings are compatible with inflammatory bowel disease and chronic active infectious colitides. Clinical correlation is suggested.
Microscopic
Features helpful for the diagnosis of IBD - as based on a study:[7]
- Basal inflammation, i.e. crypt base, plasmacytosis with severe chronic inflammation.
- Crypt architectural abnormalities.
- Atrophy = less glands ~ 3-4 glands/mm (normal = 7-8 glands/mm).
- Branching = common (normal = very rare branching).
- Distortion = bent glands, marked size variation (normal = "rack of test tubes").
- Distal Paneth cell metaplasia.
- Paneth cells should not be in the left colon[10] - 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.[11]
- Paneth cells have basal nuclei and coarse luminal granules.[12]
- They should not be confused with endocrine cells -- these have apical nuclei and fine granules.
Notes:
- Microscopic features can be remembered by mnemonic CPP: Crypts (abnormal), Plasmacytosis, Paneth cells where they don't belong.
- If you see architectural distortion (e.g. crypt branching) in the left colon, look for Paneth cells.
- The hepatic flexure is considered the divider for normal paneth cells and abnormal paneth cells, i.e. paneth cells proximal to the hepatic flexure are normal; paneth cells distal to the hepatic flexure are abnormal.[13]
- Stretching of tissue may mimic atrophy; tip-off it is artefact: thinning of mucosa.[8]
Images:
- Crohn's disease - beautiful granulomas in the colon - high mag. (WC).
- Crohn's disease - duodenum - intermed. mag. (WC).
- Cryptitis - high mag. (WC).
- Crypt branching (WC).
Grading
Grading schemes for IBD in a table
| Nil | Mild | Moderate | Severe | |
| "A grading scheme"[8] | - | cryptitis | PMN abscesses | erosions |
| Gupta[14] | "0" (nil) | "1" (<50% of crypts have PMNs) |
"2" (>50% of crypts have PMNs) |
"3" (presence of ulcers or erosions) |
Crohn's disease vs. ulcerative colitis
- Some cases cannot be classified by the experts (see "indeterminate colitis").
Robbins
UC features:[15]
- Mucosal involvement -- sometimes submucosa.
- No skip lesions.
- Colon/rectum only.
- UC may have 'ileal backwash' -- mild ileal inflammation due to backwash of inflammatory soup from colon.
- "No granulomas".
- Superficial granulomas in the mucosa are non-specific, especially if they are beside an inflammed crypt, i.e. they may be present in UC.[16][17]
- Deep granulomas are specific for Crohn's disease.
- Superficial granulomas in the mucosa are non-specific, especially if they are beside an inflammed crypt, i.e. they may be present in UC.[16][17]
Example of a superficial granuloma that is non-specific, i.e. this could be UC or CD:
Kirsch
Features of UC[8] - memory device DDDR:
- Diffuse inflammation.
- Diffuse arch. changes.
- Diffuse atrophy.
- Rectal involvement.
Words of caution
The following may be present in UC:[8]
- Cecal patch (cecal involvement without pancolitis).
- Patchy involvement
- Esp. in Tx'ed patients.
- Esp. in children.
- Ileitis - esp. in the context of severe pancolitis; known as backwash ileitis.
- Deep inflammation (in a fissure).
- Upper GI tract involvement -- see below.
Upper gastrointestinal tract involvement
- The old dogma was upper GI tract = Crohn's disease.
Characteristics of upper GI tract UC:[18]
- Most common:
- Focal gastritis.
- Mixed basal inflammation and superficial plasmacytosis in the stomach.
- Unique:
- Diffuse chronic duodenitis.
- ~ 10% of UC patients.
- ~ 40% of UC + colectomy + pouchitis.
A tabular comparison
Gross pathology:
| Feature | Crohn's disease | Ulcerative colitis |
| Lesion distribution | patchy | diffuse |
| Strictures | maybe | no |
| Perianal disease | yes/no | no |
| Rectal involvement | no | yes |
| Ileal involvement | yes, classic | usu. no; seen in pancolitis |
| Upper GI tract involvement | yes | yes (gaining acceptance) |
| Associated with PSC | not classically | yes |
Ulcerative colitis
- Often abbreviated as UC.
General
- May be associated with toxic megacolon.
Epidemiology:
- Associated with primary sclerosing cholangitis.
- Appendicitis is considered protective against UC.[19][20]
- Smoking is protective; the opposite is true for Crohn's disease.[20]
Gross
- Conventionally considered to be contiguous, i.e. no "skip lesions", with rectal involvement being most severe.
- Dependent on the study one reads... rectal sparing may be seen in 15% of UC patients.[21]
Microscopic
Features:
- Inflammation:
- Active:
- Neutrophils:
- Intraepithelial (cryptitis).†
- Clusters in crypts (crypt abscesses).
- Erosions.
- Neutrophils:
- Chronic:
- Architectural distortion.
- Basal plasmacytosis.
- Foveolar metaplasia.
- Paneth cell metaplasia (distal).
- Lack of granulomas.
- Active:
Notes:
- †Neutrophils are usually numerous in the lamina propria in minimal/mild active inflammation.
- No full wall-thickness inflammation.
- Epithelial apoptosis correlated with inflammation.[22]
DDx:
- Crohn's disease.
- Infectious colitis.
- Ischemic colitis.
Sign out
SIGMOID COLON, BIOPSY: - MILD ACTIVE COLITIS, SEE COMMENT. - NEGATIVE FOR DYSPLASIA. COMMENT: No granulomata are identified.
A. RIGHT COLON, BIOPSY: - MODERATE ACTIVE COLITIS, SEE COMMENT. - NEGATIVE FOR DYSPLASIA. B. LEFT COLON, BIOPSY: - MODERATE-TO-SEVERE CHRONIC ACTIVE COLITIS, SEE COMMENT. - NEGATIVE FOR DYSPLASIA. COMMENT: No granulomata are identified. The mucosa is diffusely inflamed. Architectural distortion is present in the left colon. The findings are consistent with ulcerative colitis; however, an infectious etiology should be considered as a possibility.
Inactive disease
SIGMOID COLON, BIOPSY: - CHRONIC COLITIS, SEE COMMENT. - NEGATIVE FOR ACTIVE COLITIS. - NEGATIVE FOR DYSPLASIA. COMMENT: The sections show chronic changes (basal plasmacytosis, marked crypt architectural distortion, crypt branching); however, no active colitis is present. Also, lamina propria neutrophils, which are often easy to identify in an active colitis, are not apparent. Appreciable numbers of lamina propria eosinophils are present and focally intraepithelial. No granulomas are identified. Clinical correlation is required.
Surveillance
A. ASCENDING COLON, BIOPSY: - COLONIC MUCOSA WITHOUT APPARENT PATHOLOGY. - NEGATIVE FOR ACTIVE COLITIS. - NEGATIVE FOR DYSPLASIA. B. TRANSVERSE COLON, BIOPSY: - COLONIC MUCOSA WITHOUT APPARENT PATHOLOGY. - NEGATIVE FOR ACTIVE COLITIS. - NEGATIVE FOR DYSPLASIA. C. DESCENDING COLON, BIOPSY: - COLONIC MUCOSA WITHOUT APPARENT PATHOLOGY. - NEGATIVE FOR ACTIVE COLITIS. - NEGATIVE FOR DYSPLASIA. D. SIGMOID COLON, BIOPSY: - COLONIC MUCOSA WITHOUT APPARENT PATHOLOGY. - NEGATIVE FOR ACTIVE COLITIS. - NEGATIVE FOR DYSPLASIA. E. RECTUM, BIOPSY: - RECTAL MUCOSA WITHOUT APPARENT PATHOLOGY. - NEGATIVE FOR ACTIVE COLITIS. - NEGATIVE FOR DYSPLASIA. COMMENT: Morphologically benign lymphoid aggregates are found focally. No granulomas are identified. Minimal architectural changes are seen focally.
A. CECUM, BIOPSY: - QUIESCENT INFLAMMATORY BOWEL DISEASE. - NEGATIVE FOR DYSPLASIA. B. ASCENDING COLON, BIOPSY: - QUIESCENT INFLAMMATORY BOWEL DISEASE. - NEGATIVE FOR DYSPLASIA. C. COLON, HEPATIC FLEXURE, BIOPSY, - QUIESCENT INFLAMMATORY BOWEL DISEASE. - NEGATIVE FOR DYSPLASIA. D. TRANSVERSE COLON, BIOPSY: - QUIESCENT INFLAMMATORY BOWEL DISEASE. - NEGATIVE FOR DYSPLASIA. E. COLON, SPLENIC FLEXURE, BIOPSY: - QUIESCENT INFLAMMATORY BOWEL DISEASE. - NEGATIVE FOR DYSPLASIA. F. DESCENDING COLON, BIOPSY: - QUIESCENT INFLAMMATORY BOWEL DISEASE. - NEGATIVE FOR DYSPLASIA. G. SIGMOID COLON, BIOPSY: - QUIESCENT INFLAMMATORY BOWEL DISEASE. - NEGATIVE FOR DYSPLASIA. H. RECTUM, BIOPSY - QUIESCENT INFLAMMATORY BOWEL DISEASE. - NEGATIVE FOR DYSPLASIA. COMMENT: No granulomas are identified. Mild architectural distortion is present. No active inflammation is identified. Scattered mucosal lymphoid nodules with germinal center formation are present.
Micro
The sections show focal intraepithelial neutrophils (cryptitis). No crypt abscesses are identified. Granulation tissue is present. There is focal Paneth cell metaplasia and foveolar metaplasia. No granulomata are identified.
Crohn's disease
- Often abbreviated as CD.
General
- Autoimmune disease.
- Increased risk for cancer - usu. rectal cancer; classically mucinous adenocarcinoma.
Associations:[23]
- High socioeconomic status.
- Family history of IBD.
- City dwellers.
- Not breastfed.
Treatment:
- Immune suppression.
- Surgery considered treatment of last resort.
Gross
- Aphthous ulcer - first gross finding of IBD.
- Transmural inflammation, i.e. full thickness of bowel wall.
- Creeping fat (also "fat wrapping" and "fat hypertrophy"[24]) - abundant fat, fat on anti-mesenteric side of the bowel.[25]
- Definition: fat on more than 50% of the intestinal surface.[24]
- DDx of creeping fat: ulcerative colitis, sclerosing mesenteritis, mesenteric panniculitis, epiploic appendagitis, omental infarction, gastrointestinal complication a renal transplant, idiopathic segmental ureteritis.[26]
- Can be seen radiologically.
- Cobblestone appearance -- may be described as such on endoscopy; due to edema.
- Serpiginous ulcers.
Notes:
- Grossly, the margins should be clear of disease; the surgical clearance and microscopic involvement are not considered important.[27]
- The term creeping fat may be used in the context of a vasculitis outside of the abdominal cavity.[26]
Microscopic
Features:[7]
- Segmental crypt architectural abnormalities.
- Mucin depletion -- less goblet cells. (???)[28]
- Mucin preservation at the active sites.
- Focal chronic inflammation without crypt atrophy.
DDx:
- Infectious colitis:
- Ulcerative colitis.
- NSAID-induced small bowel injury.[29]
- Others - a long DDx is here.[30]
Sign-out
Biopsies
A. TERMINAL ILEUM, BIOPSY - MODERATE GRANULOMATOUS ILEITIS. B. CECUM, BIOPSY: - MILD PATCHY ACTIVE CECITIS. C. SIGMOID COLON, BIOPSY: - CHRONIC INFLAMMATORY CHANGES. NO ACTIVE COLITIS. COMMENT: The histomorphological findings (patchy inflammation, granulomas, ileitis, paneth cell metaplasia, crypt loss and crypt elongation) are suggestive of Crohn's disease. An infective etiology should be considered, as it cannot be definitely excluded on pathologic grounds.
Quiescent Crohn's disease
DESCENDING COLON, BIOPSY: - COLONIC MUCOSA WITH PROMINENT LAMINA PROPRIA PLASMA CELLS. - NEGATIVE FOR ACTIVE COLITIS. COMMENT: Minimal architectural changes consistent with chronic inflammation are present. There are no granulomas. No dysplasia is identified. The findings are compatible with quiescent Crohn's disease.
Resection
TERMINAL ILEUM, CECUM, AND APPENDIX, CECUM-ILEUM RESECTION: - CHRONIC ACTIVE GRANULOMATOUS ILEITIS -- INCLUDING: -- MURAL MICROABSCESS FORMATION. -- SEROSITIS. -- A STRICTURE. -- DEEP ULCERATION (AT LEAST THROUGH THE MUSCULARIS PROPRIA). - PERIAPPENDICITIS, NEGATIVE FOR APPENDICITIS. - CECUM WITHIN NORMAL LIMITS. - TEN LYMPH NODES NEGATIVE FOR MALIGNANCY ( 0 POSITIVE / 10 ). - NEGATIVE FOR DYSPLASIA AND NEGATIVE FOR MALIGNANCY. COMMENT: The sections show patchy transmural inflammation and skip lesions. The findings are consistent with Crohn's disease.
TERMINAL ILEUM, CECUM, APPENDIX, AND ASCENDING COLON, RIGHT HEMICOLECTOMY: - CHRONIC ACTIVE ILEITIS -- INCLUDING: -- INFLAMMATORY PSEUDOPOLYP. -- STRICTURE ASSOCIATED WITH LARGE LYMPHOID AGGREGATE. - THIRTEEN LYMPH NODES NEGATIVE FOR MALIGNANCY ( 0 POSITIVE / 13 ). - NEGATIVE FOR DYSPLASIA AND NEGATIVE FOR MALIGNANCY. COMMENT: The sections show patchy transmural inflammation and skip lesions. Submucosal fibrosis is present. Focal ulceration and abscess formation is identified. No granulomas are identified. The findings are consistent with Crohn's disease.
ILEUM, COLON, ILEO-COLIC RESECTION: - SEVERE FOCAL ILEITIS WITH ULCERATION AND TRANSMURAL INFLAMMATION. - BENIGN STRICTURE ASSOCIATED WITH A LARGE LYMPHOID AGGREGATE. - FIBROUS ADHESION. - COLON WITHIN NORMAL LIMITS. - ONE LYMPH NODE NEGATIVE FOR MALIGNANCY ( 0 POSITIVE / 1 ). - NEGATIVE FOR DYSPLASIA AND NEGATIVE FOR MALIGNANCY. COMMENT: The findings are consistent with chronic, active Crohn's disease.
"Indeterminate colitis"
- "Indeterminate colitis" is a confusing term and should be avoided.[31]
Terminology
- IBDU = IBD unclassified.
- CUTE = Colitis of uncertain type or etiology.
- Should be reserved for resection specimens only.
Dysplasia-associated lesion or mass
- Abbreviated DALM.
General
- Proving invasive malignancy (on histopathologic grounds alone) in the setting of chronic inflammation is difficult.[32]
- This diagnosis depends on correlation of endoscopy and histopathology - important.[33]
- Biopsies are usually taken of the lesion and around the base.
Microscopic
Features:
- Flat or polypoid.[32]
- Cytologic dysplasia - as in adenomatous polyps.
DDx:
- Sporadic adenomatous polyp -- favouring sporadic:
Image:
Pouchitis
General
- Inflammation of an ileal pouch - a treatment for ulcerative colitis.
- Chronic pouchitis seen in approximately 15% of patients.[35]
- May be assessed by fecal calprotectin.[36]
- Considered a clinico-pathologic diagnosis.[37][35]
Microscopic
Features:[38]
- Neutrophils.
- +/-Crypt abscess - indicator of moderate or severe.
- Ulceration.
Image:
Scoring system
Pouchitis disease activity index (PDAI) - based on clinical and pathologic factors:
- Active pouchitis >= 7.
- Remission < 7.
The histologic component of the PDAI:[38]
- Neutrophils.
- Mild.
- Moderate - crypt abscesses.
- Severe - crypt abscesses.
- Ulceration per LPF (mean).
- <25%.
- 25-50%.
- >50.
See also
- Colon.
- Colorectal tumours.
- Common variable immunodeficiency.
- Gastrointestinal pathology.
- Intestinal polyps.
References
- ↑ Schmidt C, Bielecki C, Felber J, Stallmach A (June 2010). "Surveillance strategies in inflammatory bowel disease". Minerva Gastroenterol Dietol 56 (2): 189–201. PMID 20485256.
- ↑ URL: http://www.gihealthfoundation.org/library/ppts/postcolectomypatient.pdf. 3 March 2011.
- ↑ 3.0 3.1 Claessen, MM.; Siersema, PD.; Vleggaar, FP. (Apr 2011). "IBD-related carcinoma.". Best Pract Res Clin Gastroenterol 25 Suppl 1: S27-38. doi:10.1016/S1521-6918(11)70007-5. PMID 21640928.
- ↑ Vos, AC.; Bakkal, N.; Minnee, RC.; Casparie, MK.; de Jong, DJ.; Dijkstra, G.; Stokkers, P.; van Bodegraven, AA. et al. (Sep 2011). "Risk of malignant lymphoma in patients with inflammatory bowel diseases: A Dutch nationwide study.". Inflamm Bowel Dis 17 (9): 1837-1845. doi:10.1002/ibd.21582. PMID 21830262.
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) 605956
- ↑ Alvarez-Lobos M, Arostegui JI, Sans M, et al. (November 2005). "Crohn's disease patients carrying Nod2/CARD15 gene variants have an increased and early need for first surgery due to stricturing disease and higher rate of surgical recurrence". Ann. Surg. 242 (5): 693–700. PMC 1409853. PMID 16244543. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1409853/.
- ↑ 7.0 7.1 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.
- ↑ 8.0 8.1 8.2 8.3 8.4 8.5 Kirsch, R. 13 December 2010.
- ↑ "Pathology of ulcerative colitis". http://www.histopathology-india.net/UlCol.htm. Retrieved 17 January 2011.
- ↑ 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.
- ↑ 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.
- ↑ Mills, Stacey E. (2006). Histology for Pathologists (3rd ed.). Lippincott Williams & Wilkins. pp. 631. ISBN 9780781762410.
- ↑ STC. 14 December 2009.
- ↑ 14.0 14.1 Gupta RB, Harpaz N, Itzkowitz S, et al. (October 2007). "Histologic inflammation is a risk factor for progression to colorectal neoplasia in ulcerative colitis: a cohort study". Gastroenterology 133 (4): 1099–105; quiz 1340–1. doi:10.1053/j.gastro.2007.08.001. PMC 2175077. PMID 17919486. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2175077/.
- ↑ 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. 850. ISBN 0-7216-0187-1.
- ↑ Shepherd, NA. (Aug 2002). "Granulomas in the diagnosis of intestinal Crohn's disease: a myth exploded?". Histopathology 41 (2): 166-8. PMID 12147095.
- ↑ Mahadeva, U.; Martin, JP.; Patel, NK.; Price, AB. (Jul 2002). "Granulomatous ulcerative colitis: a re-appraisal of the mucosal granuloma in the distinction of Crohn's disease from ulcerative colitis.". Histopathology 41 (1): 50-5. PMID 12121237.
- ↑ Lin J, McKenna BJ, Appelman HD (November 2010). "Morphologic findings in upper gastrointestinal biopsies of patients with ulcerative colitis: a controlled study". Am. J. Surg. Pathol. 34 (11): 1672–7. doi:10.1097/PAS.0b013e3181f3de93. PMID 20962621.
- ↑ Beaugerie, L.; Sokol, H. (Aug 2009). "Appendicitis, not appendectomy, is protective against ulcerative colitis, both in the general population and first-degree relatives of patients with IBD.". Inflamm Bowel Dis. doi:10.1002/ibd.21064. PMID 19685454.
- ↑ 20.0 20.1 Timmer, A.; Obermeier, F. (2009). "Reduced risk of ulcerative colitis after appendicectomy.". BMJ 338: b225. PMID 19273505.
- ↑ Bernstein CN, Shanahan F, Anton PA, Weinstein WM (September 1995). "Patchiness of mucosal inflammation in treated ulcerative colitis: a prospective study". Gastrointest. Endosc. 42 (3): 232-7. PMID 7498688.
- ↑ Seidelin, JB.; Nielsen, OH. (2009). "Epithelial apoptosis: cause or consequence of ulcerative colitis?". Scand J Gastroenterol 44 (12): 1429-34. doi:10.3109/00365520903301212. PMID 19958058.
- ↑ Gearry, RB.; Richardson, AK.; Frampton, CM.; Dodgshun, AJ.; Barclay, ML. (Feb 2010). "Population-based cases control study of inflammatory bowel disease risk factors.". J Gastroenterol Hepatol 25 (2): 325-33. doi:10.1111/j.1440-1746.2009.06140.x. PMID 20074146.
- ↑ 24.0 24.1 Schäffler, A.; Herfarth, H. (Jun 2005). "Creeping fat in Crohn's disease: travelling in a creeper lane of research?". Gut 54 (6): 742-4. doi:10.1136/gut.2004.061531. PMID 15888774.
- ↑ Schäffler, A.; Herfarth, H. (Jun 2005). "Creeping fat in Crohn's disease: travelling in a creeper lane of research?". Gut 54 (6): 742-4. doi:10.1136/gut.2004.061531. PMID 15888774.
- ↑ 26.0 26.1 Golder, WA. (Jan 2009). "The "creeping fat sign"-really diagnostic for Crohn's disease?". Int J Colorectal Dis 24 (1): 1-4. doi:10.1007/s00384-008-0585-y. PMID 18815796.
- ↑ Hamilton, SR. (1983). "Pathologic features of Crohn's disease associated with recrudescence after resection.". Pathol Annu 18 Pt 1: 191-203. PMID 6348672.
- ↑ McCormick DA, Horton LW, Mee AS (February 1990). "Mucin depletion in inflammatory bowel disease". J. Clin. Pathol. 43 (2): 143–6. PMC 502296. PMID 2318990. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC502296/.
- ↑ Hayashi, Y.; Yamamoto, H.; Taguchi, H.; Sunada, K.; Miyata, T.; Yano, T.; Arashiro, M.; Sugano, K. (2009). "Nonsteroidal anti-inflammatory drug-induced small-bowel lesions identified by double-balloon endoscopy: endoscopic features of the lesions and endoscopic treatments for diaphragm disease.". J Gastroenterol 44 Suppl 19: 57-63. doi:10.1007/s00535-008-2277-3. PMID 19148795.
- ↑ Dilauro, S.; Crum-Cianflone, NF. (Aug 2010). "Ileitis: when it is not Crohn's disease.". Curr Gastroenterol Rep 12 (4): 249-58. doi:10.1007/s11894-010-0112-5. PMID 20532706.
- ↑ Geboes K, Colombel JF, Greenstein A, et al. (June 2008). "Indeterminate colitis: a review of the concept--what's in a name?". Inflamm. Bowel Dis. 14 (6): 850–7. doi:10.1002/ibd.20361. PMID 18213696.
- ↑ 32.0 32.1 Blackstone, MO.; Riddell, RH.; Rogers, BH.; Levin, B. (Feb 1981). "Dysplasia-associated lesion or mass (DALM) detected by colonoscopy in long-standing ulcerative colitis: an indication for colectomy.". Gastroenterology 80 (2): 366-74. PMID 7450425.
- ↑ 33.0 33.1 33.2 Neumann, H.; Vieth, M.; Langner, C.; Neurath, MF.; Mudter, J. (Jul 2011). "Cancer risk in IBD: how to diagnose and how to manage DALM and ALM.". World J Gastroenterol 17 (27): 3184-91. doi:10.3748/wjg.v17.i27.3184. PMID 21912466.
- ↑ Fogt, F.; Urbanski, SJ.; Sanders, ME.; Furth, EE.; Zimmerman, RL.; Deren, JJ.; Noffsinger, AE.; Vortmeyer, AO. et al. (Mar 2000). "Distinction between dysplasia-associated lesion or mass (DALM) and adenoma in patients with ulcerative colitis.". Hum Pathol 31 (3): 288-91. PMID 10746669.
- ↑ 35.0 35.1 Gionchetti, P.; Amadini, C.; Rizzello, F.; Venturi, A.; Poggioli, G.; Campieri, M. (Feb 2003). "Diagnosis and treatment of pouchitis.". Best Pract Res Clin Gastroenterol 17 (1): 75-87. PMID 12617884.
- ↑ Johnson, MW.; Maestranzi, S.; Duffy, AM.; Dewar, DH.; Forbes, A.; Bjarnason, I.; Sherwood, RA.; Ciclitira, P. et al. (Mar 2008). "Faecal calprotectin: a noninvasive diagnostic tool and marker of severity in pouchitis.". Eur J Gastroenterol Hepatol 20 (3): 174-9. doi:10.1097/MEG.0b013e3282f1c9a7. PMID 18301296.
- ↑ Royston, DJ.; Warren, BF. (Nov 2011). "Are we reporting ileal pouch biopsies correctly?". Colorectal Dis 13 (11): 1285-9. doi:10.1111/j.1463-1318.2010.02452.x. PMID 20958905.
- ↑ 38.0 38.1 Shen, B.; Achkar, JP.; Connor, JT.; Ormsby, AH.; Remzi, FH.; Bevins, CL.; Brzezinski, A.; Bambrick, ML. et al. (Jun 2003). "Modified pouchitis disease activity index: a simplified approach to the diagnosis of pouchitis.". Dis Colon Rectum 46 (6): 748-53. doi:10.1097/01.DCR.0000070528.00563.D9. PMID 12794576.
- ↑ Arashiro, RT.; Teixeira, MG.; Rawet, V.; Quintanilha, AG.; Paula, HM.; Silva, AZ.; Nahas, SC.; Cecconello, I. (Jul 2012). "Histopathological evaluation and risk factors related to the development of pouchitis in patients with ileal pouches for ulcerative colitis.". Clinics (Sao Paulo) 67 (7): 705-10. PMC 3400158. PMID 22892912. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3400158/.