Gastro Flashcards

1
Q

What is primary biliary cirrhosis?

A

An autoimmune disease of the liver with destruction of the bile ducts within the liver

It leads to cholestasis, scarring, fibrosis, and cirrhosis.

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2
Q

What complications can occur with primary biliary cirrhosis?

A

Osteoporosis and sicca syndrome

Sicca syndrome is characterized by dry eyes and mouth.

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3
Q

Who is more commonly affected by primary biliary cirrhosis?

A

Women, particularly those aged 30-65 years

The disease is significantly more prevalent in women.

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4
Q

What are common symptoms of primary biliary cirrhosis?

A

Fatigue, pruritus, steatorrhoea, and jaundice

Steatorrhoea refers to fatty stools due to malabsorption.

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5
Q

What examination findings may indicate primary biliary cirrhosis?

A

Complications of cirrhosis, portal hypertension, xanthelasmata, xanthomata, skin hyperpigmentation, hepatomegaly (70%), splenomegaly (35%)

.

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6
Q

In which patient demographic should primary biliary cirrhosis be suspected?

A

Middle-aged women presenting with fatigue, itching, jaundice, or right upper quadrant discomfort

These symptoms are indicative of liver dysfunction.

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7
Q

What is the hallmark of primary biliary cirrhosis?

A

The presence of antimitochondrial antibodies

These antibodies are found in 90-95% of patients with a specificity of 98% for the disease.

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8
Q

What are the goals of management for primary biliary cirrhosis?

A

To slow disease progression and alleviate symptoms such as pruritus, osteoporosis, and sicca syndrome

Management focuses on improving quality of life.

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9
Q

What is the only life-saving procedure for primary biliary cirrhosis?

A

Liver transplantation

It is indicated in advanced cases of liver failure.

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10
Q

Fill in the blank: The presence of _______ is a key indicator of primary biliary cirrhosis.

A

antimitochondrial antibodies

These antibodies help confirm the diagnosis.

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11
Q

True or False: Primary biliary cirrhosis can lead to fibrosis and cirrhosis of the liver.

A

True

The disease progresses to serious liver damage if left untreated.

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12
Q

Calculation for plasma osmolality

A

2Na+ urea+glucose

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13
Q

Drugs to use with caution in Gilbert’s

A

Atazanavir/ indinavir (HIV)
Gemfibrozil (lipids)
Irinotecann
Statins when combined with gemfibrozil
(Drugs that inhibit UDP- glucuronyl transferase)

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14
Q

Which condition causes a combination of pigmented lesions in the buccal mucosa +GI polyps?

A

Peutz-Jeghers’ syndrome

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15
Q

What is the inheritance of Peutz-Jeghers’ syndrome

A

Autosomal dominant

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16
Q

What are complications of Peutz-Jeghers’ syndrome?

A

Intestinal lesions: hamartomas
Increased risk of intestinal cancer
Bowel obstruction from intussusception
Lower GI bleeding
Prolapse of polyps

17
Q

What is Gardner syndrome

A

Familial colorectal polyposis
Autosomal dominant condition characterised by multiple polyps in the colon + tumours outside colon

18
Q

What characterises juvenile polyposis syndrome

A

Multiple polyps in GI tract of kids
Most benign but some increased risk of adenocarcinoma