7.6 Cancers of the Digestive System Flashcards

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1
Q

True or false: the mechanism of chronic liver disease is thought to be entirely separate from hepatocellular carcinoma

A
  • False
  • Most HCC arises on a background of chronic liver disease, and emerges with development of cirrhosis
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2
Q

List three classes of factors that are thought to occur with the onset of HCC, and give examples

A
  1. Toxicity (alcohol, aflatoxin)
  2. Viral infection (Hep B/C)
  3. Metabolic disease (hereditary haemochromatosis, alpha 1 antitrypsin deficiency)
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3
Q

List three mutations that may cause Hepatocellular Carcinoma

A
  • Activation of B-catenin
  • Inactivation of p53
  • Increase in IL-6
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4
Q

List three kinds of lesions that may act as precursors for HCC

A
  • Hepatocellular adenoma
  • Dysplastic nodules
  • Diffuse cell changes
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5
Q

What are hepatocellular adenomas? Are they more common in men or women? What medication are they associated with?

A
  • Benign lesions of the liver; arise in non-cirrhotic liver
  • More common in women
  • Associated w/ OCP
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6
Q

What are the two types of dysplastic nodules in the liver? Which is more likely to progress to HCC?

A
  • High grade and low grade nodules
  • High grade is more likely to progress
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7
Q

CRC is the _____ most common type of cancer in Australia. It is more common in men/women, and almost all are _______carcinomas

A
  • Third most common
  • More common in men
  • Almost all are adenocarcinomas
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8
Q

Modifiable risk factors for CRC

A
  • Smoking
  • Obesity
  • Processed meat
  • Alcohol
  • Low fibre, high refined carbs
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9
Q

List three protective factors for colorectal cancer

A
  1. Vegetarian diet
  2. High fibre diet
  3. NSAIDs
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10
Q

What is familial adenomatous polyposis (FAP)? What is its genetic nature? What is the prognosis?

A
  • Genetically, it is autosomal dominant (caused by mutation in APC gene)
  • Causes many adenomas of the colon, prophylactic colectomy indicated
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11
Q

Explain the pathophys of Lynch Syndrome. What is it also called?

A
  • Mutation in mismatch repair, causing mutations in microsatellite DNA regions affecting areas of DNA that control cell replication
  • Also called Hereditary Non-Polyposis Colorectal Cancer (HNPCC)
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12
Q

What is the genetic basis of HNPCC/Lynch Syndrome?

A
  • Patients inherit one mutant gene (usually of MSH2 or MLH1
  • These are mismatch repair genes (what’s the link to pathophysiology?)
  • When the second copy is lost, cell growth becomes out of control
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13
Q

Familial Adenomatous Polyposis typifies which aetiological mechanism of CRC?

A

Adenoma-carcinoma progression

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14
Q

What is the most common mechanism of CRC pathogenesis?

A

Progression from adenomatous polyps

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15
Q

List some non-modifiable risk factors for colorectal cancer

A
  • Family history (closer = worse)
  • FAP/HNPCC
  • IBD
  • Increasing age
  • African descent
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16
Q

General presentation symptoms for all crc

A
  • Changes in bowel habit
  • Unexpected weight loss
  • Rectal bleeding
  • Abdo pain
17
Q

Common symptoms/signs for right sided crc

A
  • Signs of anaemia (stealthy occult bleeding in proximal colon)
  • Right sided abdo pain
  • Ielocaecal valve obstruction (late)
18
Q

Common symptoms/signs for left sided crc

A
  • Rectal bleeding more common
  • Rectal mucous
  • Lower abdo colic
  • Abdo distension (late)
19
Q

CRC Ix

A
  • Bloods: CBC, EUC, LFT, ?Carcinoembryonic Antigen test (after diagnosis)
  • Foecal occult blood test (no point if bleeding)
  • Colonoscopy
  • Imaging (MRI/CT)
20
Q

Why do we resect widely in surgical management of colorectal cancer?

A
  • Tumours will drain in lymphovascular manner
  • Need to perform lymphovascular clearance (by resecting) as well
21
Q

What is one consideration if we want to ensure the colon anastomoses after CRC resection?

A

Must ensure adequate blood supply to prevent necrosis

22
Q

True or false: due to improvement in surgical tech, stoma are almost never indicated in CRC patients nowadays

A
  • False
  • Stoma may be required; not exactly uncommon
23
Q

Under what circumstances do we screen for a disease?

A
  • Can be detected early
  • Accepted treatment exists
  • Can be done acceptably, inexpensively, and sensitively