GI Flashcards

(66 cards)

1
Q

Incompetent LOS, Barrier impairment, delayed oespahgeal clearance, heartburn and waterbrash

A

GORD

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2
Q

Dyasphagia that is worse for solids than liquids

A

Benign osesphageal stricture

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3
Q

Treatment for GORD

A

1) Antacid
2) Full dose PPI
3) Step down to H2 receptor antagonists then antacids

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4
Q

More common in children, mucosal ring strictures or narrow calibrated oesophagus

A

Eosinophilic oesphagitis

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5
Q

Halitosis, gurgling and barium swallow

A

Pharyngeal Pouch

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6
Q

Manometry

A

Achalasia

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7
Q

Episodic chest pain may mimic angina, treat using PPE

A

Oesophageal spasm

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8
Q

Schatzki rings

A

Found at oesophago-gastric function–> benign strictures

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9
Q

Most common benign tumour of the oesphagus

A

Leiomyoma

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10
Q

Pathogenesis of oesophageal adenocarcinoma

A

Normal–> Oesophagitis–> Barrett’s–> Adenocarcinoma

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11
Q

HLA DQ8, Small bowel, blunting of villi, flattening of epithelium, Marsh Score, Antibody test then biopsy, Dermatitis Herpetiformis

A

Coeliac

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12
Q

Chronic, progressive malabsorption from the tropics, India, Malaysia, Indonesia, treat using tetracycline, presents similarly to coeliac disease, adults more than children

A

Tropical Sprue

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13
Q

High numbers of coliforms, watery diarrhoea and steatorrhea due to vitamin B12 deficiency, hydrogen breath tests, tetracycline

A

Small bowel overgrowth

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14
Q

Infiltration of small intestinal mucosa by “foamy” macrophages, middle aged men, PCR diagnosis, PAS positive macrophages, joint pain, arthritis, fevers, diaroea and lymphadenopathy

A

Whipple’s Disease

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15
Q

Malaborption of vitamin B12 and bile salts, need parenteral nutrition and vitamin B12 supplements. Jejunum-colon or Jejunostomy.

A

Ileal Resection and short bowel syndrome

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16
Q

Nausea, vomiting, adominal distension, alternating constipation and diarrhoea but no mechanical obstruction

A

Pseudoobstruction

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17
Q

Most common congenital abnormality of the GI tract, failure of closure of the vitelline duct, 100cm of ileocaecal valve. complications in first 2 years of life. Can mimic appenditis

A

Meckel’s Diverticulum

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18
Q

Can affect any part of GI tract, usually results from swallowing after coughing, PCR, RIPE, Granulomatous hepatitis occurs

A

Abdominal TB

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19
Q

Patient with AF and abdominal pain. “Angina of the guts”, metabolic acidosis. Most commonly embolus from heart lodges and blocks the mesenteric artery. Complications: resolution, gangrene, fibrous stricture

A

Small bowel Ichaemia

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20
Q

Acute sever abdominal pain, no abdominal signs, rapid hypovolaemia–> shock

A

Acute Small bowel Ischaemia

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21
Q

When inflammation goes into the muscle layers, it loses tone and starts to distend

A

Toxic Megacolon

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22
Q

Projective mad of scar tissue which develops from granulation tissue during healing process. Failed attempt of wall to heal naturally. Signs of previous intense inflammation

A

Pseudopolyps

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23
Q

Rome Criteria and FODMAP

A

IBS

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24
Q

Uncommon, autosomal dominant, APC gene, 90% of patients develop CRC by age 50

A

Familial Ademomatous Polyps

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25
Multiple hamartomatous polyps can occur in intestine and colon. Melanin pigementation of lips, mouth and digits. Autosomal dominant
Peutz-Jeghers Syndrome
26
1/3rd inherited in autosomal recessve manner, harmatous polyps, 20% develop CRC before age 40
Juvenile Polyps
27
Gastric pits elongated with replacement of parietal and chief cells with mucus secreting cells
Menetrier's Disease
28
Autoimmune damage to parietal cells, gastric atrophy and loss of intrinsic factor leading to pernicious anaemia. Most commonly caused by H.pylori
Autoimmune Chronic Gastritis
29
Ulcer at first part of duodenum on anterior wall
Chronic Duodenal ulcer
30
Ulcer where 90% are located at the lesser curve within the antrum or at the junction between the body and astral mucosa
Chronic Gastric Ulcer
31
Gram negative spiral bacteria, lives between mucus layers, gastric type epithelium, provokes local inflammatory response, causes depletion of somatostatin and increased G cell secretion
H.pylori
32
Board like rigitity, sever, sudden pain, upper abdomen generally, free air under diaphragm
Peritonitis
33
Abdominal discomfort, satiety and loading after meals. Overlap between peptic ulcers and IBS
Dyspepsia
34
Defective gastric emptying wihtout mechanical obstruction
Gastroparesis
35
Pathogenesis of Stomach cancer
Normal--> Chronic Gastritis--> Chronic Gastritis Atropy, Intestinal Metaplasia, Dysplasia, Neoplasia
36
Grey Turner's Sign or Cullen's Sign, GETSMASHED, Enzyme mediated autodigestion
Acute Pancreatitis
37
A collection of fluid may accumulate in the lesser sac following inflammatory rupture of the pancreatic duct. After 6 weeks, this matures to form a fibrous cap. This can compress into surrounding structures
Pancreatic fluid collection develops into Pseudocyst causing pseudoaneurysm
38
Raised serum amylase
Acute Pancreatitis
39
Fibrosis and destruction of exocrine pancreatic tissue. Diabetes mellitus occurs in later stages. Alcohol misuse, middle ages men. Loss of exocrine function. Thin, malnourished with epigastric pain and skin pigmentation (chronic use of hot water bottle)
Chronic Pancreatitis
40
Most cpmmon Pancreatic carcinoma
Adenocarcinoma
41
Palpable gallbladder
Courvoiser's Sign
42
Disrupted and dilated anal cushions, typically at 3,7,11 o'clock. Fresh bright red blood, painless. Band ligation, sclerosants.
Haemorrhoids
43
Tear in the anal canal due to passage of a constipated stool, "like passing glass through pack passage". GTN ointment to relax sphincter
Anal Fissure
44
A tract communictaes between the skin and anal canal and presents as an abscess which doesn't heal. Glued or "Laid open"
Anal Fistula
45
The mucosa may protrude through the anal canal. Bleeding and mucus PR. Incontinence and poor anal tone
Rectal Prolapse
46
Abdominal pain, rebound tenderness, absent bowel sounds, high neutrophil count, broad spectrum antibiotics,, paracentesis required for diagnosis
Spontanous Bacterial Peritonitis
47
Faecal oral, over crowding and poor sanitation. No chronic infection. Gold top serology.
Hepatitis A
48
Chronic infection is common. Progression from chronic hepatitis to cirrhosis occurs 20-40 years
Hepatitis C
49
Similar presentation to Hepatitis A
Hep C
50
Liver is enlarged, even in presence of cirrhosis
Alcoholic Liver Disease
51
Syndromes of Alcoholic Liver disease
Fatty Liver, Alcoholi Liver Disease and Cirrhosis
52
2 hit pathogenesis
1) Steatosis 2) Steatohepatitis -NAFLD
53
Insidious onset, ASMA and AMA
Autoimmune Type 1
54
Anti LKM
Autoimmune Type 2
55
Middle aged women, insidious onset, IgM elevation. AMA. Ursodexycholic acid
Primary Biliary Cirrhosis
56
Onion skin fibrosis, young men, high risk of CRC
Primary Sclerosing Cholangitis
57
Malignant hepatocytes surrounded by dense fibrous storm, no Hep B or Cirrhosis. Surgical Resection
Fibrolamellar Hepatocellular carcinoma
58
Most common benign liver tumours, asymptotic, diagnosis by US then CT
Haemangiomas
59
Fever, rigors, leukocytosis, abdominal pain in RUQ. Due to biliary obstruction or empyema of gallbladder. Needle aspiration under US. Empirical broad spectrum antibiotics with pus drainage.
Liver Abscess
60
Requires weekly venesection
Haemochromatosis
61
Requires lifelong Penicillamine
Wilsons
62
Autosomal dominant, mutation in promoter region of UDP-glucuonyl transferase. Decreased conjugation of bilirubin and accumulation of unconjugated bilirubin
Gilbert's Syndrome
63
Large bowel: TH1 and TH2 mediated TH1 mediated
- 1&2 UC | - 1 Crohn's
64
ROME criteria
Used in IBS
65
- Bleeding PR - Obstruction occurs early - Tenesmus and altered bowel habit
Left sided colorectal cancer
66
- Weight loss | - Anaemia
Right sided colorectal cancer