Gi Flashcards

(50 cards)

1
Q

Classification used for GORD

A

Los Angeles classification

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2
Q

Metaplasia of squamous to columnar epithelium following chronic GORD

A

Barrett’s oesophagus

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3
Q

Risk factors of oesophageal adenocarcinoma

A

Male
Caucasian
Barett’s oesophagus

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4
Q

Risk factors for squamous cell carcinoma

A
Alcohol and smoking 
Achalasia of cardia 
Plummer vinson syndrome 
Nutritional deficiencies 
Nitrosamines 
HPV
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5
Q

Ethnicity risk factor for Squamous cell oesophageal carcinoma

A

Afrocarribean

M>f

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6
Q

What is stomach lined by?

A

Gastric mucosa
Columnar epithelium
Glands

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7
Q

MHC class of coeliac disease

A

DQ2

Dq8 HLA

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8
Q

Rash seen in coeliac disease

A

Dermatitis herpetiforms

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9
Q

Serological tests to do in coeliac disease

A

Anti endomysial (best spec and sen)

Anti tissue transglutaminase (IgA)
Anti gliadin (Poor marker of disease control)
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10
Q

Gold standard ix of coeliac disease

A

Upper GI endoscopy and duodenal biopsy

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11
Q

What is seen on duodenal biopsy of coeliac disease

A

Villous atrophy
Crypt hyperplasia
Lymphocyte infiltrate

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12
Q

Cancer associated with coeliac disease

A

Duodenal T cell lymphoma

10% progress to this

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13
Q

Location of volvulus in elderly

A

Sigmoid > caecal

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14
Q

Location of volvulus in infants

A

Small bowel

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15
Q

Common location of bowel is charm is

A

Water shed areas
Eg splenic flexure (where the superior mesenteric artery transitions into the inferior mesenteric artery)

Rectosigmoid (where the inferior mesenteric artery transitions into the internal iliac artery)

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16
Q

Abx that increase risk of C. difficile

A

Cipro

Ceph

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17
Q

Tx of C. difficile

A

Metronidazole

2nd line is vancomycin

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18
Q

Investigation for C. difficile

A

Stool culture

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19
Q

Cell origin of tumours causing carcinoid syndrome

A

Enterochromaffin cell origin

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20
Q

What do enterchronaffin cells produce in carcinoid syndrome which causes the symptoms

A

Serotonin (5HT3)

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21
Q

Investigation of choice for carcinoid syndrome

A

24 hour urine 5-HIAA (which is a metabolite of serotonin)

22
Q

Treatment of carcinoid syndrome

A

Octreotide

This is a somatostatin analogue

23
Q

What do villous adenomas cause

A

Hypoproteinasmjc hypokalaemia

Because they leak large amounts of protein and potassium

24
Q

Risk factors for malignancy in adenomas

A

Large size (over 3.4cm)
Degree of dysplasia
Increased villous component

25
Adenoma to carcinoma sequence
Normal colon is at risk after first hit mutation in the 1st APC gene (those born with FAP have this mutation) Second hit to the remaining APC gene Progression to carcinoma following activation of KRAS, LOF, mutations of p53
26
Juvenile polyposis - autosomal dominant and recessive
Autosomal dominant
27
Mutated gene in Peutz Jeghers syndrome
LKB1 | Autosomal dominant
28
Symptoms and signs of Peutz Jeghers syndrome
Multiple polyps Mucocutaneous hyperpigmentation Freckles around mouth, palm and soles
29
What are those with Peutz Jeghers syndrome at risk of
Intussuception | Malignancy so regular surveillance of GI tract, pelvis, and gonads
30
Age group hyperplastic polyp seems in
50-60 years
31
What type of cancer are the majority of colorectal cancers
98% adenocarcinoma
32
Most colorectal carcinoma’s are located in
Rectum (45%)
33
What is protective for colorectal carcinoma
NSAIDs | COX2 is overexpressed in 90% of cases
34
Clinical feature of right sided colorectal cancer
Anaemia (iron deficiency) | Weight loss
35
Clinical features of left sided colorectal cancer
Weight loss Change in bowel habit Crampy LLQ pain
36
What can be measured after diagnosis of colorectal cancer to monitor disease
``` Carcinoembryonic antigen (CEA) This is raised But not very specific or sensitive to be used as a screening tool ```
37
Staging used for colorectal cancer
Duke’s staging TNM can also be used A, B1-2, C1-2, D
38
Type of surgery carried out for colorectal cancer if tumour is <1-2cm above anal sphincter (lower 1/3 of rectum)
Abdominoperineal resection
39
Type of surgery carried out to remove colorectal cancer tumour >1-2 cm above anal sphincter
Anterior resection
40
Operation for sigmoid cancer
Sigmoid colectomy
41
What treatment given post op for colorectal cancer to decrease local recurrence
Radiotherapy
42
What chemo drug used to tx colorectal cancer
5-FU | Fluorouracil
43
Autosomal DOm or recessive - familial adenomatous polyposis
Autosomal dominant
44
Gene commonly affected in familial adenomatous polyposis
APC gene (70%) - C5q1 A.R. mutation in DNA Mismatch repair genes in 30% cases
45
Number of polyps required for diagnosis of familial adenomatous polyps
>100 adenomatous polyps
46
At birth, what is seen in patients with familial adenomatous polyposis
Hypertrophy of retinal pigment epithelium
47
What is Gardner’s
Familial syndrome similar to familial adenomatous polyposis but also with extra GI features eg Dental carries Osteomas
48
Hereditary non polyposis colorectal cancer / lynch syndrome - AD or AR
Autosomal dominant | Mutation in DNA mismatch repair genes
49
Where do carcinomas usually arise in HNPCC
Right colon | There are few polyps but they Rogers to malignancy fast (<50 years)
50
Cancers associated with HNPCC
Endometrial Ovarian Small bowel Transitional cell and stomach carcinoma