Difference between revisions of "Gastrointestinal tract polyps"

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'''Intestinal polyps''' are often the bread & butter of a GI pathologists workload.  Some of 'em are benign... some pre-malignant... some malignant... some weird.
'''Intestinal polyps''' are often the bread & butter of a GI pathologists workload.  Some of 'em are benign... some pre-malignant... some malignant... some weird.


Overview - there are four basic types:<ref>PBoD P.856</ref>
Overview - there are four basic types:<ref>{{Ref PBoD|856}}</ref>
*Hyperplastic - harmless, most common - 90% of all colonic polyps.<ref>PBoD P.858.</ref>
*Hyperplastic - harmless, most common - 90% of all colonic polyps.<ref>{{Ref PBoD|858}}</ref>
*Hamartomatous - weriod stuff, syndromic things.
*Hamartomatous - weriod stuff, syndromic things.
*Inflammatory - think [[inflammatory bowel disease]], aka ''pseudopolyps''.
*Inflammatory - think [[inflammatory bowel disease]], aka ''pseudopolyps''.
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{{familytree | | | | | H | | I | | J |H=TA|I=TVA|J=VA}}
{{familytree | | | | | H | | I | | J |H=TA|I=TVA|J=VA}}
{{familytree/end}}
{{familytree/end}}
Notes:<ref>PBoD P.860.</ref>  
Notes:<ref>{{Ref PBoD|860}}</ref>  
*TA, tubular component >75%.
*TA, tubular component >75%.
*VA, villous component >50%.
*VA, villous component >50%.
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==Hyperplastic polyp==
==Hyperplastic polyp==
*Most common colonic polyp (90% of all colonic polyps<ref>PBoD P.858.</ref>).
*Most common colonic polyp (90% of all colonic polyps<ref>{{Ref PBoD|858}}</ref>).


===Microscopy===
===Microscopy===
Features:<ref>PBoD P.858</ref>
Features:<ref>{{Ref PBoD|858}}</ref>
*Irregular crypt architecture - tortuosity.
*Irregular crypt architecture - tortuosity.
*Serrated epithelial cells (at the surface of the gland).
*Serrated epithelial cells (at the surface of the gland).
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====Typing====
====Typing====
Subclassified as:<ref name=pbod860>PBoD P.860.</ref>
Subclassified as:<ref name=pbod860>{{Ref PBoD|860}}</ref>
*Tubular (most common), tubular component >75%.
*Tubular (most common), tubular component >75%.
*Villous (least common ~= 1% of (traditional) adenomas), villous component >50%.
*Villous (least common ~= 1% of (traditional) adenomas), villous component >50%.
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====Microscopic====
====Microscopic====
Features:<ref>PBoD P.859</ref><ref>[http://www.nature.com/modpathol/journal/v16/n4/fig_tab/3880773f4.html http://www.nature.com/modpathol/journal/v16/n4/fig_tab/3880773f4.html]</ref>
Features:<ref>{{Ref PBoD|859}}</ref><ref>[http://www.nature.com/modpathol/journal/v16/n4/fig_tab/3880773f4.html http://www.nature.com/modpathol/journal/v16/n4/fig_tab/3880773f4.html]</ref>
*Eroded, smooth or lobulated surface.
*Eroded, smooth or lobulated surface.
*Pedunculated.
*Pedunculated.
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===Peutz-Jeghers polyp===
===Peutz-Jeghers polyp===
====Clinical/Epidemiology====
====Clinical/Epidemiology====
Features:<ref>PBoD P.859.</ref><ref>[http://www.nature.com/modpathol/journal/v16/n4/fig_tab/3880773f4.html http://www.nature.com/modpathol/journal/v16/n4/fig_tab/3880773f4.html]</ref>
Features:<ref>{{Ref PBoD|859}}</ref><ref>[http://www.nature.com/modpathol/journal/v16/n4/fig_tab/3880773f4.html http://www.nature.com/modpathol/journal/v16/n4/fig_tab/3880773f4.html]</ref>
*Peutz-Jeghers syndrome is autosomal dominant.
*Peutz-Jeghers syndrome is autosomal dominant.
*Altered gene: STK11.
*Altered gene: STK11.


====Microscopy====  
====Microscopy====  
Features:<ref>PBoD P.859.</ref><ref>[http://www.nature.com/modpathol/journal/v16/n4/fig_tab/3880773f4.html]</ref>
Features:<ref>{{Ref PBoD|859}}</ref><ref>[http://www.nature.com/modpathol/journal/v16/n4/fig_tab/3880773f4.html]</ref>
*Frond-like polyp with all three components of mucosa:
*Frond-like polyp with all three components of mucosa:
*# Muscosal epithelium (melanotic mucosa, goblet cells).
*# Muscosal epithelium (melanotic mucosa, goblet cells).
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===Cowden disease===
===Cowden disease===
Features:<ref>PBoD P.858-9.</ref>
Features:<ref>{{Ref PBoD|858-9}}</ref>
*Hamartomatous polyps  
*Hamartomatous polyps  
*Facial trichilemmomas (hair follicle root sheath epithelium tumour),  
*Facial trichilemmomas (hair follicle root sheath epithelium tumour),  
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===Cronkhite-Canada syndrome===  
===Cronkhite-Canada syndrome===  
Features:<ref>PBoD P.858-9.</ref>
Features:<ref>{{Ref PBoD|858-9}}</ref>
*Hamartomatous polyps,  
*Hamartomatous polyps,  
*Ectodermal abnormalities (nail atrophy, skin pigment, alopecia).
*Ectodermal abnormalities (nail atrophy, skin pigment, alopecia).
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