Histopathology 16: Lower GI Flashcards

(37 cards)

1
Q

A 2 year old boy with down syndrome presents with symptoms of constipation with overflow diarrhoea and vomiting. There are signs of abdominal distension.

What is the most likely diagnosis ?

A

Hirschsprung’s disease

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2
Q

Where does Volvulus tend to occur in children? Where does it occur in adults ?

A
Children= small bowel 
Adults = Sigmoid colon
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3
Q

Which organism causes pseudomembranous colitis ?

A

C.difficile

antibiotics kill commensal bacteria and allow C.diff to flourish. It’s endotoxins cause Pseudomembranous colitis

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4
Q

List features of Crohn’s disease ?

A
  • ENTIRE GIT affected (mainly terminal ileum and large bowel)
  • Transmural inflammation (all the way through the wall)
  • Skip lesions
  • Non-caseating granulomas
  • Cobblestone mucosa
  • Can affect anus to mouth
  • Fistula formation

Extra-intestinal (NB also get these in UC):

  • Arthritis
  • Uveitis
  • Stomatitis/ cheilitis
  • Skin lesions: erythema multiforme, nodosum
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5
Q

List 5 features of Ulcerative colitis ?

A
  • Involves rectum and Colon but not small bowel
  • Inflammation confined to the mucosa (NOT transmural like Crohn’s)
  • Inflammation is continuous, no skip lesions
  • Backwash ileitis- terminal ileum gets involved
  • Can cause toxic megacolon
  • ULCERS
  • mucosa regenerates forming pseudopolyps
  • Crypt abscesses
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6
Q

List 3 skin lesions seen in Crohn’s ?

A

Erythema multiforme
Erythema nodosum
Pyoderma gangrenosum

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7
Q

List 3 familial syndromes characterised by polyps ?

A

Familial adenomatous polyposis
Peutz-jeghers syndrome
Hereditary non polyposis colorectal cancer (HNPCC)

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8
Q

Name 2 subtypes of FAP ?

A

Gardner’s syndrome
Turcot syndrome

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9
Q

List 5 extra-intestinal manifestations of Gardner’s syndrome ?

A

Gardner’s syndrome: pathological and aetiological features of FAP with a high cancer risk

  • Multiple Osteomas of the skull and mandible
  • Epidermal cysts
  • Desmoid tumours
  • Dental carries/ unerrupted supernumerary teeth
  • Post surgical mesenteric fibromatoses
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10
Q

List 3 features seen in carcinoid syndrome ?

A
  • Flushing
  • Diarrhoea
  • Bronchoconstriction / tachycardia
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11
Q

Which test is used to diagnose carcinoid syndrome ?

A
  • 24 hour urine 5-HIAA
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12
Q

Which paediatric disease presents with up to 100 hamartomatous polyps in children <5 years old ?

A

Juvenile polyposis

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13
Q

List 3 features of peutz-jeghers syndrome ?

A
  • multiple hamartomatous polyps
  • freckles around mouth
  • mucocutaenous hyperpigmentation
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14
Q

Which staging system is used to stage colorectal adenocarcinoma?

A

Duke’s staging

  • A= confined to bowel wall
  • B= through wall of bowel
  • C= lymph node metastases
  • D= distant metastases
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15
Q

Which tumour marker identifies colorectal cancer ?

A

CEA

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16
Q

where do 90% of diverticuli occur

17
Q

therapy for pseudomembranous colitis

A

metronidazole or vancomycin

18
Q

at what sites do ischaemic colitis/ infarction occur

A
  • segments in ‘watershed’ zones
  • such as splenic flexure (SMA and IMA), rectosigmoid (IMA and IIA)
19
Q

list causes of ischaemic colitis

A
  • arterial occlusion
  • venous occlusion
  • small vessel disease - DM, cholesterol, emboli, vasculitis
  • low flow states - shock, haemorrhage
  • obstruction - hernia, intussusception, adhesions
20
Q

list 3 complications of UC

A
  • severe haemorrhage
  • toxic megacolon
  • adenocarcinoma
21
Q

list some extra-intestinal features of UC (5)

A

arthritis
myositis
uveitis/iritis
Erythema Nodosum, PG
PSC

22
Q

list 3 non neoplastic polyps of the colon and rectum

A

hyperplastic
inflammatory (pseudo-polyps)
hamartomatous (juvenile, peutz jeghers)

23
Q

list 3 neoplastic polyps (increase R of cancer) of the colon and rectum

A

tubular adenoma
tubulovillous adenoma
villous adenoma

24
Q

list risk factors for the development of cancer from a polyp

A

size of polyp (>4cm - 455 have invasive malignancy)
proportion of villous component (more villousy = more R)
degree of dysplastic change within the polyp

25
what is FAP/APC
AD average age of onset = 25 yrs minimum 100 polyps (average 1000) chromosome 5q21, APC TS gene nearly 100% develop cancer within 10 years
26
What is Hereditary Non-Polyposis Colorectal Cancer (HNPCC)?
* autosomal DOMINANT condition (uncommon) * Numerous DNA replication errors * Get Onset of colorectal cancer at an early age * High frequency of carcinomas proximal to the splenic flexure * Multiple synchronous cancers (also endometrium, prostate, breast, stomach) * Do NOT necessarily get polyps
27
Is UC or Crohn's more common?
UC (slightly more)
28
Mutation causing Familial Adenomatous Polyposis (FAP)
APC tumour suppressor gene on Chromosome 5q21 (FAP gene)
29
Where is high frequency of carcinomas in HNPCC found?
proximal to the splenic flexure
30
Most colon cancers are what type? Sx
adenocarcinoma (98%) - means they come from the glands * Bleeding * Change in bowel habit * Anaemia * Weight loss * Pain * Fistula
31
Big RF for diverticular disease
low-fibre diet High intraluminal pressure leads to herniation of the bowel mucosa through weak points in the bowel wall
32
How to detect C. difficile toxin in Pseudomembranous Colitis
toxin stool assay
33
Most common vascular disorder of the intestinal tract
Ischaemic Colitis/ Infarction
34
What are GIT adenomas?
* excessive epithelial proliferations with dysplasia (moving towards cancer) * has lost control but it has NOT invaded yet so it is not cancer
35
Histology of Tubular Adenoma
Has stalk + not invaded basement membrane
36
On histology, difference between pink and purple
Pink = good Purple = bad
37
Progression of normal cells to carcinoma in GIT
* Normal -\> adenoma -\> carcinoma * Adenomas tend to appear about 10 years before carcinoma * Risk of cancer is proportional to the number of the adenomas * Screening and removal of adenoma reduces risk of carcinoma