General Gastrointestinal Medicine Flashcards

1
Q

What are the causes of dysphagia?

A

They fall into 3 broad categories; mechanical block, motility disorders and others.

Mechanical Block:
Malignant strictures (oesophageal, gastric or pharyngeal cancer)
Benign strictures (oesophageal web or peptic stricture)
Extrinsic pressure (lung cancer, mediastinal lymph nodes, retrosternal goitre, aortic aneurysm or left atrial enlargement)
Pharyngeal pouch
Motility Disorders:
Achalasia
Diffuse oesophageal spasm
Systemic sclerosis
Neurological bulbar palsy
pseudobulbar palsy
Wilson's or Parkinson's Disease
Syringobulbia
Bulbar poliomyelitis
Chagas' Disease
Myasthenia gravis

Others:
Oesophagitis
Globus

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2
Q

What is dysphagia?

A

Difficulty swallowing.

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3
Q

What is odynophagia?

A

Painful swallowing.

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4
Q

What is Zollinger-Ellison syndrome?

A

Zollinger-Ellison syndrome is condition characterised by excessive levels of gastrin, usually from a gastrin secreting tumour usually of the duodenum or pancreas. Around 30% occur as part of MEN type I syndrome

Features
multiple gastroduodenal ulcers
diarrhoea
malabsorption

Diagnosis
fasting gastrin levels: the single best screen test
secretin stimulation test

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5
Q

What are the organs affected in MEN- type 1?

A

parathyroid (95%): hyperparathyroidism due to parathyroid hyperplasia
pituitary (70%)
pancreas (50%, e.g. Insulinoma, gastrinoma)
also: adrenal and thyroid

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6
Q

What are the differences between Crohn’s and ulcerative colitis?

A

Crohn’s disease (CD)

Features

  • Diarrhoea usually non-bloody
  • Weight loss more prominent
  • Upper gastrointestinal symptoms, mouth ulcers, perianal disease
  • Abdominal mass palpable in the right iliac fossa

Extra-intestinal

  • Gallstones are more common secondary to reduced bile acid reabsorption
  • Oxalate renal stones*

Complications

  • Obstruction
  • fistula
  • colorectal cancer

Pathology

  • Lesions may be seen anywhere from the mouth to anus
  • Skip lesions may be present

Histology
- Inflammation in all layers from mucosa to serosa
increased goblet cells
- granulomas

Endoscopy

  • Deep ulcers
  • skip lesions
  • ‘cobble-stone’ appearance
Radiology	
- Small bowel enema
- high sensitivity and specificity for examination of the terminal ileum
strictures: 
- 'Kantor's string sign'
proximal bowel dilation
- 'rose thorn' ulcers
- fistulae

Ulcerative colitis (UC)

Features

  • Bloody diarrhoea more common
  • Abdominal pain in the left lower quadrant
  • Tenesmus

Extra-intestinal
- Primary sclerosing cholangitis more common

Complications
- Risk of colorectal cancer high in UC than CD

Pathology

  • Inflammation always starts at rectum and never spreads beyond ileocaecal valve
  • Continuous disease

Histology
- No inflammation beyond submucosa (unless fulminant disease) - inflammatory cell infiltrate in lamina propria
neutrophils migrate through the walls of glands to form crypt abscesses
- depletion of goblet cells and mucin from gland epithelium
- granulomas are infrequent

Endoscopy
- Widespread ulceration with preservation of adjacent mucosa which has the appearance of polyps (‘pseudopolyps’)

Radiology

  • Barium enema
  • loss of haustrations
  • superficial ulceration
  • ‘pseudopolyps’
  • long standing disease: colon is narrow and short -‘drainpipe colon’
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7
Q

What is Whipple’s disease?

A

Whipple’s disease is a rare multi-system disorder caused by Tropheryma whippelii infection. It is more common in those who are HLA-B27 positive and in middle-aged men

Features

  • malabsorption: diarrhoea, weight loss
  • large-joint arthralgia
  • lymphadenopathy
  • skin: hyperpigmentation and photosensitivity
  • pleurisy
  • pericarditis
  • neurological symptoms (rare): ophthalmoplegia, dementia, seizures, ataxia, myoclonus

Investigation
- jejunal biopsy shows deposition of macrophages containing Periodic acid-Schiff (PAS) granules

Management
- guidelines vary: oral co-trimoxazole for a year is thought to have the lowest relapse rate, sometimes preceded by a course of IV penicillin

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8
Q

How should a paracetamol overdose be managed?

A

Acetylcysteine should be given if:
there is a staggered overdose or there is doubt over the time of paracetamol ingestion, regardless of the plasma paracetamol concentration; or
the plasma paracetamol concentration is on or above a single treatment line joining points of 100 mg/L at 4 hours and 15 mg/L at 15 hours, regardless of risk factors of hepatotoxicity

Acetylcysteine is now infused over 1 hour (rather than the previous 15 minutes) to reduce the number of adverse effects.

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9
Q

What is the King’s College Hospital criteria for liver transplantation in paracetamol overdose?

A

Arterial pH < 7.3, 24 hours after ingestion

or all of the following:
prothrombin time > 100 seconds
creatinine > 300 µmol/l
grade III or IV encephalopathy

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10
Q

What is the presentation of congestive hepatomegaly?

A

The liver only usually causes pain if stretched. One common way this can occur is as a consequence of congestive heart failure. In severe cases cirrhosis may occur.

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11
Q

What is the presentation of biliary colic?

A

RUQ pain, intermittent, usually begins abruptly and subsides gradually. Attacks often occur after eating. Nausea is common.

It is sometimes taught that patients are female, forties, fat and fair although this is obviously a generalisation.

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12
Q

What is the presentation of acute cholecysitits?

A

Pain similar to biliary colic but more severe and persistent. The pain may radiate to the back or right shoulder.

The patient may be pyrexial and Murphy’s sign positive (arrest of inspiration on palpation of the RUQ)

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13
Q

What is the presentation of ascending cholangitis?

A

An infection of the bile ducts commonly secondary to gallstones. Classically presents with a triad of:

  • fever (rigors are common)
  • RUQ pain
  • jaundice
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14
Q

What is the presentation of gallstone ileus?

A

This describes small bowel obstruction secondary to an impacted gallstone. It may develop if a fistula forms between a gangrenous gallbladder and the duodenum.

Abdominal pain, distension and vomiting are seen.

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15
Q

What is the presentation of cholangiocarcinoma?

A

Persistent biliary colic symptoms, associated with anorexia, jaundice and weight loss. A palpable mass in the right upper quadrant (Courvoisier sign), periumbilical lymphadenopathy (Sister Mary Joseph nodes) and left supraclavicular adenopathy (Virchow node) may be seen

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16
Q

What is the presentation of acute pancreatitis?

A

Usually due to alcohol or gallstones
Severe epigastric pain
Vomiting is common
Examination may reveal tenderness, ileus and low-grade fever
Periumbilical discolouration (Cullen’s sign) and flank discolouration (Grey-Turner’s sign) is described but rare

17
Q

What is the presentation of pancreatic cancer?

A

Painless jaundice is the classical presentation of pancreatic cancer. However pain is actually a relatively common presenting symptom of pancreatic cancer. Anorexia and weight loss are common

18
Q

What is the presentation of amoebic liver abscess?

A

Typical symptoms are malaise, anorexia and weight loss. The associated RUQ pain tends to be mild and jaundice is uncommon.

19
Q

Clostridium difficile features?

A
  • diarrhoea
  • abdominal pain
  • a raised white blood cell count is characteristic
  • if severe toxic megacolon may develop
20
Q

Clostridium difficile treatment?

A
  • first-line therapy is oral metronidazole for 10-14 days
  • if severe or not responding to metronidazole then oral vancomycin may be used
  • for life-threatening infections a combination of oral vancomycin and intravenous metronidazole should be used
21
Q

Wilson’s disease features?

A
  • liver: hepatitis, cirrhosis
  • neurological: basal ganglia degeneration, speech and behavioural problems are often the first manifestations.
  • Also: asterixis, chorea, dementia
    Kayser-Fleischer rings
    renal tubular acidosis (esp. Fanconi syndrome)
    haemolysis
    blue nails
22
Q

Wilson’s disease diagnosis?

A
  • reduced serum caeruloplasmin

- increased 24hr urinary copper excretion

23
Q

Wilson’s disease management?

A
  • penicillamine (chelates copper) has been the traditional first-line treatment
  • trientine hydrochloride is an alternative chelating agent which may become first-line treatment in the future
  • tetrathiomolybdate is a newer agent that is currently under investigation
24
Q

What is the most common cause of traveller’s diarrhoea?

A

Escherichia coli

25
Q

What are the typical causes of acute food poisoning?

A
  • Staphylococcus aureus
  • Bacillus cereus
  • Clostridium perfringens