Difference between revisions of "Stomach"
(→Hyperplastic polyp: more) |
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*S100 -ve. | *S100 -ve. | ||
== | ==Gastric hyperplastic polyp== | ||
===General=== | ===General=== | ||
*Benign. | *Benign. | ||
*Most common gastric polyp.<ref name=pmid19037727/> | |||
===Microscopic=== | ===Microscopic=== | ||
Line 507: | Line 508: | ||
*No hyperchromasia. | *No hyperchromasia. | ||
*No loss of pseudostratification. | *No loss of pseudostratification. | ||
Notes: | |||
*No serrations - as in the colon. | |||
DDx: | DDx: | ||
*[[Ménétrier's disease]]<ref name=pmid18384215>{{Cite journal | last1 = Park | first1 = do Y. | last2 = Lauwers | first2 = GY. | title = Gastric polyps: classification and management. | journal = Arch Pathol Lab Med | volume = 132 | issue = 4 | pages = 633-40 | month = Apr | year = 2008 | doi = 10.1043/1543-2165(2008)132[633:GPCAM]2.0.CO;2 | PMID = 18384215 | url=http://www.archivesofpathology.org/doi/full/10.1043/1543-2165(2008)132%5B633:GPCAM%5D2.0.CO;2 }}</ref> (hyperplastic hypersecretory gastropathy). | *[[Ménétrier's disease]]<ref name=pmid18384215>{{Cite journal | last1 = Park | first1 = do Y. | last2 = Lauwers | first2 = GY. | title = Gastric polyps: classification and management. | journal = Arch Pathol Lab Med | volume = 132 | issue = 4 | pages = 633-40 | month = Apr | year = 2008 | doi = 10.1043/1543-2165(2008)132[633:GPCAM]2.0.CO;2 | PMID = 18384215 | url=http://www.archivesofpathology.org/doi/full/10.1043/1543-2165(2008)132%5B633:GPCAM%5D2.0.CO;2 }}</ref> (hyperplastic hypersecretory gastropathy). | ||
*[[Juvenile polyp]].<ref name=pmid19037727>{{Cite journal | last1 = Jain | first1 = R. | last2 = Chetty | first2 = R. | title = Gastric hyperplastic polyps: a review. | journal = Dig Dis Sci | volume = 54 | issue = 9 | pages = 1839-46 | month = Sep | year = 2009 | doi = 10.1007/s10620-008-0572-8 | PMID = 19037727 }}</ref> | |||
*[[Peutz-Jeghers polyp]]. | *[[Peutz-Jeghers polyp]]. | ||
Images: | |||
*www: | |||
**[http://www.flickr.com/photos/jian-hua_qiao_md/3953137621/ Gastric hyperplastic polyp (flickr.com)]. | |||
**[http://www.flickr.com/photos/jian-hua_qiao_md/3953138195/in/photostream/ Gastric hyperplastic polyp (flickr.com)]. | |||
*[[WC]]: | |||
**[http://en.wikipedia.org/wiki/File:Gastric_hyperplastic_polyp_%281%29_foveolar_type.jpg Gastric hyperplasia - low mag. (WC)]. | |||
**[http://en.wikipedia.org/wiki/File:Gastric_hyperplastic_polyp_%283%29_foveolar_type.jpg Gastric hyperplasia - high mag. (WC)]. | |||
==Adenomatous polyps== | ==Adenomatous polyps== |
Revision as of 00:49, 7 December 2011
Stomach is an important organ for pathologists. It is often inflamed and may be a site that cancer arises from. Gastroenterologists often biopsy the organ. Surgeon take-out the organ. It connects the esophagus to the duodenum. An introduction to gastrointestinal pathology is in the gastrointestinal pathology article.
Normal
Gross anatomy
- Cardia - first part of the stomach; joins with esophagus.
- Fundus - superior portion - not attached directly to the esophagus.
- Body - contains parietal cells.
- Pylorus - distal (think pyloric stenosis); it joins with the duodenum.
- AKA antrum.
Image: Stomach anatomy (WP).
Microscopic
Foveolar cells vs. intestinal goblet cells
- Intestinal goblet cells - clear mucin.
- Foveolar cells - eosinophilic contents.
Stomach vs. intestine[1]
Intestine | Stomach | |
Spacing | Goblets cell - spaced | Foveolar cells - beside one another |
Morphology of epithelial cells | columnar | tall columnar (Champagne flute) |
Vesicle at luminal surface | touching/small opening | wide open |
PAS-D | -ve (???) | +ve (???) |
Villin stain[2] | +ve | -ve |
Images | Tubular adenoma - goblet cells on right of image (WC) |
Gastric biopsy (microscopy-uk.org.uk) |
Notes:
- Intraepithelial lymphocytes in the gastric mucosa have a clear halo around 'em.[3]
- Memory device: Folveolar cells have friends, i.e. they are close to other foveolar cells.
Ref.
- PMID 11984877.
Gastric antrum vs. gastric body
Body | Antrum | Histology | Image | |
Parietal cells | abundant | few or none | parietal cells: intensely eosinophilic cytoplasm |
[1], [2] |
Chief cells | present | absent | chief cells: basophilic cytoplasm, IHC: +ve for pepsinogen I |
[3] |
G cells | absent | present | fried egg appearance (clear cytoplasm, round nucleus); look at high power - usu. middle 1/3 of gland,[4] IHC: +ve for gastrin. |
[4] |
Surface | flat | blunted villi | antrum is somewhat duodenum-like |
body - flat |
Gastric glands / mucosa |
thick | thin | not so useful for discrimination |
body - thick, body & antrum |
Notes:
- G cells may superficially resemble intraepithelial lymphocytes.
- G cell nucleus is usu. perfectly round and slightly larger (diameter of 12 micrometers?) than a lymphocyte nucleus (diameter ~ 9-10 micrometers?).
Introduction
Useful stains for stomach
- Cresyl violet stain[5] - used to find H. pylori.[6]
- Alcian blue - used to find mucin[7] which is present in intestinal metaplasia
- Other mucins stains:[8] mucicarmine, PAS, PASD (doesn't stain glycogen)
Things to look for...
- Parietal cells (indicate you're in the body of the stomach) - pink (eosinophilic) cytoplasm.
- Lack of parietal cells -- DDx: Bx of antrum (pylorus), Bx of cardia, pernicious anemia.
- Goblet cells = intestinal metaplasia.
- Architectural distortion of gastric glands - suspect cancer.
- Signet ring cells = (usually) gastric carcinoma.
- Can be very easy to miss in some biopsies.
- Inflammation + small bacteria = suspect H. pylori gastritis.
Non-neoplastic disease
Gastritis
Etiology
A specific cause is uncommonly identified histologically.
Gastritis causes:[9]
- Infectious:
- H. pylori infection.
- Tuberculosis.
- Salmonellosis.
- CMV.
- Endocrine-related:
- Pernicious anemia.
- Diabetes - gastric atony.
- Trauma, e.g. NG tube.
- Vascular, ischemia.
- Autoimmune:
- Toxins:
- Radiation.
Endoscopic appearance
- Erythematous.
Microscopic
- Inflammatory cells - see below.
Acute gastritis
- AKA active gastritis.
Features:
- Neutrophils - especially when intraepithelial.
Chronic gastritis
Features:
- Plasma cells (in lamina propria).
- Various criteria:
- Two plasma cells kissing, i.e. two plasma cells touching/overlapping.
- Three is a crowd, i.e. three plasma cells in close proximity.
- Various criteria:
Lymphocytic gastritis
The DDx is limited:
- Helicobacter gastritis.
- Celiac disease.
- NSAIDs.
- Idiopathic.
Sydney criteria for gastritis
A bunch of pathologists in Sydney came-up with criteria... and these were revised in Houston.[10]
Classification
Updated Sydney classification:[10]
Non-atrophic Helicobacter | Atrophic Helicobacter | Autoimmune | |
Inflammation pattern | antral or diffuse | antrum & corpus, mild inflammation | corpus only |
Atrophy & metaplasia | nil | atrophy present, metaplasia at incisura | corpus only |
Notes:
- Corpus = gastric body.
- Incisura = angular incisure, incisura angularis (Latin) - notched transition point on lesser curvature of the stomach between pylorus and body.[11]
Severity
The Sydney group suggests grading severity with the following language:[10]
- Mild.
- Moderate.
- Marked.
These terms are applied to the parameters described in a biopsy. The Sydney criteria lists H. pylori, neutrophils, mononuclear cells, antrum (atrophy), corpus (atrophy) and intestinal metaplasia. The paper that discusses this also give a visual analogue scale.
Parameters & Severity (adapted from Dixon et al.[10]):
Mild | Moderate | Marked | |
H. pylori | few touching | many touching | piles |
Neutrophils | few | bunches | crowded |
Mononuclear cells | not touching | kissing | partying |
Helicobacter gastritis
General
- Several Helicobacter species can cause gastritis; H. pylori most common
Finding Helicobacter
- Small - smaller than the nucleus of the gastric foveolar cell.
- On 400x they are still possible to miss.
- Commonly have a "v" shape.
- Look close to the opening of the gastric glands.
- Are often are found in groups.
- Location - can be antrum and/or body.[12]
- Helicobacter don't like the intestinal mucosa or mucosa that has undergone intestinal metaplasia -- you're unlikely to find 'em there.
Images:
- H. pylori - IHC (WC).
- Helicobacter gastritis:
- Set of images - HP gastritis (WC).
Epidemiologic associations
Helicobacter infections are associated with:[13]
- Gastritis.
- Peptic ulcers.
- Cancer.
- Carcinoma.
- MALT lymphoma.
Intestinal metaplasia
General
- Often part of surgical pathology report, e.g. "negative for intestinal metaplasia" or "intestinal metaplasia present".
- May be associated with Helicobacter spp. infection -- though Helicobacter don't like intestinal type mucosa, i.e. H. pylori are not typically found in regions with intestinal metaplasia.
Significance
- Moderate risk increase for carcinoma; risk less than for Barrett's esophagus.[14]
Microscopic
Features:
- Goblet cells are present in the stomach.[15]
- With cresyl violet vacuole stains blue.
- With H&E vacuole may stain greyish.
Image:
Inflammatory bowel disease & the stomach
- Histopathologic findings are usually non-specific.
- Conventional thinking was upper GI involvement = Crohn's disease; this is changing.[16]
Microscopic
Features:[17]
- Focal inflammation.
- Common finding - non-specific.
- +/-Granulomas.
Miscellaneous
This is a grab bag of stuff seen in the stomach. Some of it is quite rare.
Gastric antral vascular ectasia
General
- Abbreviated GAVE.
- Antrum lesion - due dilated capillaries.
- AKA watermelon stomach - due to characteristic endoscopic appearance.[18]
Gross/endoscopic appearance
- Linear red streaks in antrum - oriented toward the pyloric valve... vaguely resembles a watermelon.
Endoscopic images:
Microscopic
Features:[19]
- Fibrin thrombi - characteristic feature.
- Dilated capillaries in lamina propria.
Images:
Reactive gastropathy
General
- AKA chemical gastropathy,[20] incorrectly referred to as chemical gastritis (see below).
- May be seen in the context of a previous resection/surgical reconstruction, e.g. Billroth II.
Epidemiology
Associated with:[21]
- Excess acid.
- EtOH.
- Bile.
- H. pylori.
- Drugs:[20]
- Iron (brown pigment on histology).
- NSAIDs - synergistic effect with corticosteroids.
Drugs that cause erosions and/or ulcers -- adapted from Genta:[20]
Drug | Comment | Indication for Rx |
---|---|---|
NSAIDs | common cause | pain, reduce cardiovascular risk |
Corticosteroids | synergistic effect with NSAIDs | rheumatologic diseases + others |
Potassium (KCl) | common cause | renal failure |
Bisphophonates | uncommon cause | osteoporosis |
Ferrous sulfate | very common if symptomatic | iron deficiency anemia |
Chloroquine | uncommon | only in the context of malaria |
Sodium polystyrene sulfonate (Kayexalate) | rare | renal failure patients |
Relation to gastritis
- May mimic a (true) gastritis symptomatically and visually in an endoscopic examination.
- "Chemical gastritis" is misnomer. Etymologically, the -itis in gastritis, implies an inflammatory process. Chemical gastropathy is not (predominantly) an inflammatory process.
- This type of confusion is not uncommon. Steatohepatitis is another example of this; it is not a process with significant inflammation yet, confusingly, carries the -itis ending.
Microscopic
- Foveolar hyperplasia.
- Tortuosity of glands in the "neck" region of the gastric glands.
- Associated with "mucin depletion" - cytoplasm not clear -- as is usual.
- Smooth muscle fibre hyperplasia.
- Abundant eosinophilic lamina propria.
- Scant acute & chronic inflammatory cells.
Additional features.
- +/-Edema.
- +/-Erosions.
Notes:
- Triad rarely present; mild inflammation common.
DDx:
Images:
Gastric atrophy
General
- Has a wide differential diagnosis.
Microscopic
Can take three general forms:
- Intestinal metaplasia - see intestinal metaplasia section.
- Pseudopyloric metaplasia; gastric body looks like gastric antrum.
- Characterized by foveolar hyperplasia.
- Cell loss without replacement.
- Clue is deep inflammation in the body.
Lymphocytic gastritis
General
DDx:
- Celiac disease.
- Check duodenum.
- H. pylori.
- HIV/AIDS.
Microscopic
Features:[23]
- 25 lymphocytes / 100 epithelial cells.
Pernicious anemia
General
- Gastric atrophy.
- Loss of parietal cells.
- Intrinsic factor antibodies present in serum.
- Intrinsic factor -- absorbs vitamin B12.
- Macrocytic anemia.
Microscopic
Features:
- Corpus predominant inflammation.
- Increased G cells in the antrum.
- Increased gastrin level to try and stimulate (missing) parietal cells.
- See gastric atrophy section.
Collagenous gastritis
General
- Very rare.
- Associated with collagenous colitis.
Microscopic
Features:
- Eosinophilic material (collagen) expands lamina propria.
- Band of collagen must be ~thick as RBC diameter.
- Proven by trichrome stain that highlights collagen.
- Band of collagen must be ~thick as RBC diameter.
Granulomatous gastritis
- Usual DDx of granulomatous disease (see Basics article):
- DNF AAII:
- Drugs, Neoplasms, Foreign body, Autoimmune, Allergic, Infectious, Idiopathic.
- DNF AAII:
Important ones:
- Autoimmune - Crohn's disease.
- Infectious - Tuberculosis.
- Idiopathic - Sarcoidosis.
Plasma cells in the stomach
DDx of plasmacytosis:
- Plasma cell neoplasm.
- Syphilis.
- Chronic gastritis.
Gastritis cystitis profunda
General
- AKA Gastritic cystica profunda. (???)
- May be assoc. with glandular proliferation as well.[24] (???)
- Super rare.
- Similar to cystitis cystica.
Microscopic
Features:
- Cystic spaces lined by foveolar epithelium.
Ménétrier's disease
General
- Super rare.
- Increased risk of gastric adenocarcinoma.[25]
Microscopic
Features:[25]
- Foveolar cell hyperplasia - key feature.
DDx:
Gastric polyps
Similar to colonic polyps - see intestinal polyps.
DDx polyp (similar to colon & rectum):
- Hyperplastic - most common, characterised by abundant elongated foveola + glands.
- Hamartomatous - weriod stuff.
- Inflammatory fibroid polyp - inflammation, myxoid stroma.
- Fundic gland polyp - cystic dilation, flat epithelium.
- Adenomatous polyp.
Inflammatory fibroid polyp
General
- Benign.
- Through-out GI tract.
- Can be thought of as granulation tissue-like.[27]
Microscopic
Features:[28]
- Proliferating spindle cells (fibroid) - key feature.
- Inflammation:
- Eosinophils - often prominent.
- +/-Leiomyoma/schwannoma-like areas - with nuclear palisading.[27]
- +/-Vascular for fibrous tissue.
DDx:
Notes:
- Concentric = share the same centre.[30]
Images:
IHC
Features:[28]
- CD34 +ve.
- There is a CD34 -ve variant.
- Vimentin +ve -- diffuse.[31]
Others:
- CD117 -ve.
- S100 -ve.
Gastric hyperplastic polyp
General
- Benign.
- Most common gastric polyp.[32]
Microscopic
Features:[33]
- Abundant foveolar cells and elongated glands - key features.
Negatives:
- No atypical nuclei.
- No hyperchromasia.
- No loss of pseudostratification.
Notes:
- No serrations - as in the colon.
DDx:
- Ménétrier's disease[34] (hyperplastic hypersecretory gastropathy).
- Juvenile polyp.[32]
- Peutz-Jeghers polyp.
Images:
- www:
- WC:
Adenomatous polyps
General
- Divided into "gastric" and "intestinal type". (???)
- Can be grouped various ways.[34] (???)
Microscopic
- Type.
- Intestinal: goblet cells or Paneth cells.
- Gastric: foveolar epithelium. (???)
- Architectural crowding of glands.
- Hyperchromasia of cytoplasm.
- Nuclear changes:
- Loss of nuclear polarity.
- Incr. NC ratio.
- Elongation of nucleus.
Fundic gland polyp
General
- Fundic location - duh!
Clinical significance
- Weak association with FAP (familial adenomatous polyposis).[35]
- Associated with chronic proton pump inhibitors (PPI) use -- approximately 4x risk.[36]
Notes:
- Animal studies suggested PPIs cause neuroendocrine tumours -- but this has not been found in humans.[37]
Microscopic
Features:[38]
- Polypoid shape (may not be appreciated on microscopy).
- Dilated gastric glands.
- Flatted epithelial lining (consisting of normal foveolar epithelium) - key feature.
Image:
Notes:
- The presence of dysplastic changes should prompt consideration of FAP.
Neoplastic
Gastric dysplasia
General
- Criteria similar to those in adenomatous colonic polyps (see Microscopic).
- Divided into:
- Low grade.
- High grade.
- Nuclei no longer stratified.
Microscopic
Features:
- Nuclear changes.
- Nuclear crowding/pseudostratification.
- Elongation of nuclei (cigar-shaped nuclei).
- Cytoplasm - hyperchromatic.
- Mitosis - particularly above the basement membrane.
Images:
- High grade gastric dysplasia - low mag. (WC).
- High grade gastric dysplasia - very high mag. (WC).
- Gastric adenoma (WC).
Neoplastic rare
Gastric calcifying fibrous tumour
Gastric cancer
Gastric lymphoma
General
- Associated with helicobacter infection.[39]
- Usually MALT lymphoma (mucosa-associated lymphoid tissue lymphoma).
Microscopic
Features:
- Sheets of lymphoid cells.
- "Lymphoepithelial lesion" - gastric crypts invaded by a monomorphous population of lymphocytes.[40]
- Features:
- Cluster of lymphocytes - three cells or more - key feature.
- Single lymphocytes don't count.
- Clearing around the lymphocyte cluster.
- Cluster of lymphocytes - three cells or more - key feature.
- Associated with MALT lymphoma;[41] however, not specific.
- Features:
IHC - work-up
- Panker -- most useful.
Others:
- CD3, CD20, CD138, kappa, lambda, BCL2.
Treatment
- Triple therapy (two antibiotics, proton pump inhibitor (PPI)).[42]
- Surgery - if triple therapy fails.
Review paper: PMID 16950858.
Familial gastric carcinoma
Gastric carcinoma
General
Epidemiology:
- Associated with helicobacter infections, i.e. helicobacter gastritis.
- Prognosis is often poor as it is discovered at a late stage.
- Higher prevalence in countries in the far east (e.g. Japan) - thought to be environmental, e.g. diet.
Treatment:
- Surgical excision.
- Proximal tumours may require a complete gastrectomy as the stomach is innervated from its proximal part.
Classification
- Two different classification schemes.
Microscopic
Features - variable, either of the two following:
- "Typical adenocarcinoma":
- Gland-forming lesion that infiltrates into the lamina propria or beyond.
- Nuclear pleomorphism - common.
- +/-Signet ring carcinoma.
- Scattered single cells in the lamina propria or beyond with:
- Abundant cytoplasm containing one large (mucin-filled) vacuole.
- A peripheral nucleus (displaced by the vacuole).
- Scattered single cells in the lamina propria or beyond with:
Images:
IHC
CK7 +ve. CK20 -ve, occasionally +ve.
See also
References
- ↑ ALS. 4 Feb 2009.
- ↑ Osborn M, Mazzoleni G, Santini D, Marrano D, Martinelli G, Weber K (1988). "Villin, intestinal brush border hydrolases and keratin polypeptides in intestinal metaplasia and gastric cancer; an immunohistologic study emphasizing the different degrees of intestinal and gastric differentiation in signet ring cell carcinomas". Virchows Arch A Pathol Anat Histopathol 413 (4): 303–12. PMID 2459839.
- ↑ Sternberg H4P 2nd Ed., P.484
- ↑ URL: http://www.lab.anhb.uwa.edu.au/mb140/CorePages/GIT/git.htm. Accessed on: 3 December 2010.
- ↑ http://www.histology-world.com/stains/stains.htm
- ↑ Goggin N, Rowland M, Imrie C, Walsh D, Clyne M, Drumm B (December 1998). "Effect of Helicobacter pylori eradication on the natural history of duodenal ulcer disease". Arch. Dis. Child. 79 (6): 502-5. PMC 1717771. PMID 10210995. http://adc.bmj.com/cgi/pmidlookup?view=long&pmid=10210995.
- ↑ http://www.histology-world.com/stains/stains.htm
- ↑ http://www.histology-world.com/stains/stains.htm
- ↑ 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. 812-3. ISBN 0-7216-0187-1.
- ↑ 10.0 10.1 10.2 10.3 Dixon MF, Genta RM, Yardley JH, Correa P (October 1996). "Classification and grading of gastritis. The updated Sydney System. International Workshop on the Histopathology of Gastritis, Houston 1994". Am. J. Surg. Pathol. 20 (10): 1161-81. PMID 8827022. http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0147-5185&volume=20&issue=10&spage=1161.
- ↑ http://en.wikipedia.org/wiki/Angular_incisure
- ↑ Maaroos HI, Kekki M, Villako K, Sipponen P, Tamm A, Sadeniemi L (October 1990). "The occurrence and extent of Helicobacter pylori colonization and antral and body gastritis profiles in an Estonian population sample". Scand. J. Gastroenterol. 25 (10): 1010-7. PMID 2263873.
- ↑ 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. 814. ISBN 0-7216-0187-1.
- ↑ Correa P, Piazuelo MB, Wilson KT (March 2010). "Pathology of gastric intestinal metaplasia: clinical implications". Am. J. Gastroenterol. 105 (3): 493–8. doi:10.1038/ajg.2009.728. PMC 2895407. PMID 20203636. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2895407/?tool=pubmed.
- ↑ URL: http://esynopsis.uchc.edu/eAtlas/GI/1280.htm. Accessed on: 16 August 2010.
- ↑ 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.
- ↑ RK. 13 December 2010.
- ↑ Chatterjee S (July 2008). "Watermelon stomach". CMAJ 179 (2): 162. doi:10.1503/cmaj.080461. PMC 2443230. PMID 18625989. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=18625989.
- ↑ 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. 118. ISBN 978-0443066573.
- ↑ 20.0 20.1 20.2 20.3 Genta, RM. (Nov 2005). "Differential diagnosis of reactive gastropathy.". Semin Diagn Pathol 22 (4): 273-83. PMID 16939055.
- ↑ ALS. 5 February 2009.
- ↑ El-Zimaity. 18 October 2010.
- ↑ El-Zimaity. 18 October 2010.
- ↑ URL: http://www.springerlink.com/content/u2v2525241754557/ Accessed on: 19 November 2010.
- ↑ 25.0 25.1 25.2 Mitchell, Richard; Kumar, Vinay; Fausto, Nelson; Abbas, Abul K.; Aster, Jon (2011). Pocket Companion to Robbins & Cotran Pathologic Basis of Disease (8th ed.). Elsevier Saunders. pp. 410. ISBN 978-1416054542.
- ↑ Junnarkar SP, Sloan JM, Johnston BT, Laird JD, Irwin ST (May 2001). "Cronkhite-Canada syndrome". The Ulster medical journal 70 (1): 56–8. PMC 2449205. PMID 11428328. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2449205/.
- ↑ 27.0 27.1 27.2 Tadrous, Paul.J. Diagnostic Criteria Handbook in Histopathology: A Surgical Pathology Vade Mecum (1st ed.). Wiley. pp. 138. ISBN 978-0470519035.
- ↑ 28.0 28.1 Daum, O.; Hatlova, J.; Mandys, V.; Grossmann, P.; Mukensnabl, P.; Benes, Z.; Michal, M. (May 2010). "Comparison of morphological, immunohistochemical, and molecular genetic features of inflammatory fibroid polyps (Vanek's tumors).". Virchows Arch 456 (5): 491-7. doi:10.1007/s00428-010-0914-8. PMID 20393746.
- ↑ Template:Ref GI
- ↑ URL: http://dictionary.reference.com/browse/concentric. Accessed on: 29 November 2011.
- ↑ Kolodziejczyk, P.; Yao, T.; Tsuneyoshi, M. (Nov 1993). "Inflammatory fibroid polyp of the stomach. A special reference to an immunohistochemical profile of 42 cases.". Am J Surg Pathol 17 (11): 1159-68. PMID 8214261.
- ↑ 32.0 32.1 Jain, R.; Chetty, R. (Sep 2009). "Gastric hyperplastic polyps: a review.". Dig Dis Sci 54 (9): 1839-46. doi:10.1007/s10620-008-0572-8. PMID 19037727.
- ↑ URL: http://pathologyoutlines.com/stomach.html#hyperplastic. Accessed on: 26 July 2011.
- ↑ 34.0 34.1 Park, do Y.; Lauwers, GY. (Apr 2008). "Gastric polyps: classification and management.". Arch Pathol Lab Med 132 (4): 633-40. doi:10.1043/1543-2165(2008)132[633:GPCAM]2.0.CO;2. PMID 18384215. http://www.archivesofpathology.org/doi/full/10.1043/1543-2165(2008)132%5B633:GPCAM%5D2.0.CO;2.
- ↑ Freeman HJ (March 2008). "Proton pump inhibitors and an emerging epidemic of gastric fundic gland polyposis". World J. Gastroenterol. 14 (9): 1318-20. PMID 18322941. http://www.wjgnet.com/1007-9327/14/1318.asp.
- ↑ Jalving M, Koornstra JJ, Wesseling J, Boezen HM, DE Jong S, Kleibeuker JH (November 2006). "Increased risk of fundic gland polyps during long-term proton pump inhibitor therapy". Aliment. Pharmacol. Ther. 24 (9): 1341-8. doi:10.1111/j.1365-2036.2006.03127.x. PMID 17059515.
- ↑ Masaoka T, Suzuki H, Hibi T (May 2008). "Gastric epithelial cell modality and proton pump inhibitor". J Clin Biochem Nutr 42 (3): 191-6. doi:10.3164/jcbn.2008028. PMC 2386521. PMID 18545640. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386521/.
- ↑ URL: http://moon.ouhsc.edu/kfung/jty1/opaq/PathQuiz/A2B001-PQ01-M.htm. Accessed on: 19 October 2010.
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- ↑ LAUREN P (1965). "THE TWO HISTOLOGICAL MAIN TYPES OF GASTRIC CARCINOMA: DIFFUSE AND SO-CALLED INTESTINAL-TYPE CARCINOMA. AN ATTEMPT AT A HISTO-CLINICAL CLASSIFICATION". Acta Pathol Microbiol Scand 64: 31–49. PMID 14320675.
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