Histopathology 16: Lower GI Flashcards

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. Didnt pass meconium in first 24h of life

What is the most likely diagnosis ?

A

Hirschsprung’s disease - most common congenital GI abnormality

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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 ? diagnosis?

A

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

TOXIN STOOL ASSAY

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4
Q

List 5 features of Crohn’s disease ?

A
Transmural inflammation 
Skip lesions 
Non-caseating granulomas 
Cobblestone mucosa 
Can affect anus to mouth
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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
Inflammation is continuous, no skip lesions
Backwash ileitis- terminal ileum gets involved
Can cause toxic megacolon

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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

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 cancer ? describe the stages?

A

Duke’s staging

A - confined to mucosa

B1 - Extends to muscularis propia
B2 - Transmural invasion

B1 - Extends to muscularis propia + LN INVOLVEMENT
B2 - Transmural invasion + LN INVOLVEMENT

D = Distant Mets

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15
Q

Which tumour marker identifies colorectal cancer ?

A

CEA

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16
Q

Where does ischaemic colitis occur usually?

A

watershed zones - supplied by 2 vessels

Splenic flexure + rectosigmoid areas

17
Q

What are the complications associated w/ UC?

A

Toxic megacolon

20-30x risk of adenocarcinoma

18
Q

What are some extra-intestinal manifestations of IBD?

A
Arthritis
Uveitis
Stomatitis/ chelitis
Pyoderma gangrenosum
Erythema nodosum
19
Q

What are the different polyp types?

A

Polyps = benign dysplastic lesions that are often precursors to adenocarcinomas

tubular
tubulovillous
villous - greatest risk of malignant transformation

20
Q

What factors determine the risk of malignant transformation in a polyp?

A

Polyp type - villous (greatest risk)

Polyp size

Polyp degree of dysplasia

21
Q

What are colorectal cancers, how common in UK?

A

98% = adenocarcinomas

2nd most common cancer death in UK

22
Q

RFs for colorectal cancer?

A

Low fibre, high fat diet, no exercise, obesity, chronic IBD

23
Q

What are the inherited lower GI conditions that increase risk of colorectal cancer? inheritance? mx?

A

FAP

Gardeners syndrome

Hereditary Non-polyposis Colorectal Cancer / Lynch Syndrome

inheritance = AD

mx = MONITORING + TOTAL COLECTOMY

24
Q

What are the main features of FAP?

A

Lots of polyps - ~1000

APC tumour suppressor geneonchromosome 5q21

100% will have cancer within 10-15 years

25
Q

What are the main features of gardeners syndrome?

A

Subtype of FAP with extra-intestinal manifestations:

Osteomas of the skull and mandible, epidermoid cysts, desmoid tumours, dental caries, unerupted supernumerary teeth

NB QUESTIONS MAY DESCRIBE POOR DENTITION

26
Q

What are the main features of Hereditary Non-polyposis Colorectal Cancer / Lynch Syndrome (AD)?

A

Defective DNA mismatch repair

Another extra-colonic cancer at the same time – endometrium, breast, prostate, stomach

27
Q

VSA1: A 20 year old man was admitted following a 6 day history of diarrhoea, abdominal pain and weight loss. A colon biopsy revealed granulomata.

What is the most likely diagnosis?

A

Crohn’s Disease

No non-caseating granulomas in ulcerative colitis

28
Q

VSA2: What is the diagnostic test for C. diff infection?

A

Toxin stool assay

29
Q

VSA3: Mutation in which gene is present in Familial Adenomatous Polyposis?

A

APC (Adenomatous polyposis coli) – tumour suppressor gene