Histopathology - Lower GI tutorial Flashcards
Hirschsprung’s disease: what is it? how is it diagnosed? how is it managed?
Absence of ganglion cells in the myenteric plexus
Ix: rectal biopsy
Mx: anorectal pull through
Ix of choice for pseudomembranous colitis
C.difficile stool assay
Which areas of the GIT does ischaemic colitis tend to efffect?
Watershed areas e.g. splenic flexure (SMA and IMA) and rectosigmoid (IMA and internal iliac artery)
Causes of lower GI obstruction
Adhesions
Volvulus
External mass
Hernia
Difference between UC and crohn’s
crohn’s: can affect anywhere from mouth to anus, skip lesions, transmural inflammation, non-caseating granulomas
UC: large bowel only, anus upwards, inflammation confined to mucosa
Histology of Crohn’s
Non-caseating granulomas
Fat wrapping
Cobblestone mucosa
Linear ulcers
Extra GI manifestations of IBD
Arthritis Uveitis Stomatitis Pyoderma gangrenosum, erythema multiforme, erythema nodosum PSC (UC)
Main complications of UC
Toxic megacolon
Haemorrhage
Adenocarcinoma (20-30x risk)
How can polyps be classified?
Non-neoplastic and neoplastic
Non-neoplastic polyps (3)
Hamartomatous (Peutz Jeghers), hyperlastic, inflammatory
Neoplastic polyps
Tubular adenoma
Villous adenoma
Tubulovilous adenoma
Feature of neoplastic polyps
Dysplastic
Which kind of polyp do we worry about and why
Adenoma - adenocarcinoma
Risk factors for adenomas to develop into adenocarcinomas?
Size of polyp
Proportion of villous component
Degree of dysplastic change within polyp
Process in which adenomatous polyp results in adenocarcinoma
Adenoma-carcinoma sequence