4- Abdominal cancer Flashcards

1
Q

Colorectal (bowel) cancer background

A
  • 4th most prevalent cancer in UK (behind breast, prostate and lung)
  • Anywhere from colon to rectum
  • Small bowel and anal cancers less common
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2
Q

types of colorectal cancer

A

Types
- Adenocarcinomas (rarer types inc lymphoma, carcinoid (think flushing) and sarcoma)
- Adenomas may be present for 10 years before becoming cancerous

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3
Q

risk factors for colorectal cancer

A

Hereditary factors

  • Family history of bowel cancer
  • Familial adenomatous polyposis (FAP)
  • Hereditary nonpolyposis colorectal cancer (HNPCC), also known as Lynch syndrome
  • Inflammatory bowel disease (Crohn’s or ulcerative colitis)
  • Increased age

Modifiable

  • Diet (high in red and processed meat and low in fibre)
  • Obesity and sedentary lifestyle
  • Smoking
  • Alcohol

Protective

  • aspirin or NSAIDS
  • HRT
  • statin use
  • physical activirty
  • whole grains
  • dietary fibre
  • fish intake
  • tree nuts
  • vitamins D,C and others
  • calcium supplements
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4
Q

presentation of colorectal cancer

A
  • Change in bowel habit (usually to more loose and frequent stools)
  • Unexplained weight loss
  • Rectal bleeding
  • Unexplained abdominal pain
  • Iron deficiency anaemia (microcytic anaemia with low ferritin)
  • Abdominal or rectal mass on examination
  • Presenting with obstruction
    o Tumour blocks passage through bowel- surgical emergency
  • Right side colon cancer: abdominal pain, iron def anaemia, palpable mass in RIF or on PR exam
  • Left side colon cancer: rectal bleeding, change in bowel habit, tenesmus, palpable mass in LIF
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5
Q

Red flags for colorectal cancer

A
  • Change in bowel habit (usually to more loose and frequent stools)
  • Unexplained weight loss
  • Rectal bleeding
  • Unexplained abdominal pain
  • Iron deficiency anaemia (microcytic anaemia with low ferritin)
  • Abdominal or rectal mass on examination
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6
Q

referral for colorectal cancer

A

2- week wait
- Over 40 years with abdominal pain and unexplained weight loss
- Over 50 years with unexplained rectal bleeding
- Over 60 years with a change in bowel habit or iron deficiency anaemia

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7
Q

Familial adenomatous polyposis (FAP)

A
  • Autosomal dominant condition involving malfunctioning of the tumour suppressor genes called adenomatous polyposis coli (APC).
  • It results in many polyps (adenomas) developing along the large intestine.
  • These polyps have the potential to become cancerous (usually before the age of 40).

Management
- Patients have their entire large intestine removed prophylactically to prevent the development of bowel cancer (panproctocolectomy).

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8
Q

Hereditary nonpolyposis colorectal cancer (HNPCC)

A
  • Lynch syndrome.
  • Autosomal dominant condition that results from mutations in DNA mismatch repair (MMR) genes.
  • Patients are at a higher risk of a number of cancers, but particularly colorectal cancer.
  • Unlikely FAP, it does not cause adenomas and tumours develop in isolation.
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9
Q

people with FAP or Lynch are offered

A

These patients offered FIT screening at regular intervals

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10
Q

classification for bowel cancer

A

Dukes’ Classification
Dukes’ classification is the system previously used for bowel cancer. It has now been replaced in clinical practice by the TNM classification, but you may come across it in older textbooks or question banks. A brief summary is:
* Dukes A – confined to mucosa and part of the muscle of the bowel wall
* Dukes B – extending through the muscle of the bowel wall
* Dukes C – lymph node involvement
* Dukes D – metastatic disease

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11
Q

Investigations for colorectal cancer

A
  • Bloods- FBC (microcytic – iron def anaemia), LFTs, clotting, carcinoembryonic antigen (CEA)- tumour marker
    o CEA tumour marker for bowel cancer
    o Not helpful in screening, but can be used for predicting relapse
  • Colonoscopy with biopsy- gold standard- biopsy if lesion found
  • Sigmoidoscopy (if only features of rectal bleeding)

- CT colonography- pts less fit for colonoscopy- less detailed doesn’t allow for biopsy

- Staging CT scan
o CT thorax, abdomen and pelvis (CT TAP)

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12
Q

management of colorectal cancer

A

MDT approach
* Surgeons
* Oncologists
* Radiologists
* Histopathology
* Specialist nurse

Choice of managed depends on
* Clinical condition
* General health
* Stage
* Histology
* Patient wishes

Options (in any combination)
* Surgical resection
* Chemotherapy
* Radiotherapy
* Palliative care- stenting

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13
Q

Screening for colorectal cancer

A

Faecal Immunochemical Test (FIT) for asymptomatic
- Ages 60-74yo every 2 years
- If results positive –>colonoscopy

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14
Q

how does FIT testing work

A
  • Faecal immunochemical tests (FIT) look very specifically for the amount of human haemoglobin in the stool.
  • FIT replaced the older stool test called the faecal occult blood (FOB) test, which detected blood in the stool but could give false positives by detecting blood in food (e.g., from red meats).
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15
Q

how are FIT tests also used in GP

A
  • FIT tests can be used as a test in general practice to help assess for bowel cancer in specific patients who do not meet the criteria for a two week wait referral, for example:
  • Over 50 with unexplained weight loss and no other symptoms
  • Under 60 with a change in bowel habit
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16
Q

surgical resection of colorectal cancer

A

Ideal to surgically remove entire tumour – potentially curative. Can also be used palliatively- reduce size of tumour and improve symptoms
- Laparoscopic surgery gives better recovery and few complications than open surgery
- Robotic surgery used increasingly

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17
Q

what does colorectal cancer surgery involve

A
  • Identify tumour (may have been tattooed in endoscopy)
  • Remove section of bowel containing tumour
  • Creating an end-to- end anastomosis (sewing the remaining ends back together)
  • Creating a stoma if end to end not possible
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18
Q

Complications of colorectal bowel resection

A

There is a long list of potential complications of surgery for bowel cancer:

  • Bleeding, infection and pain
  • Damage to nerves, bladder, ureter or bowel
  • Post-operative ileus
  • Anaesthetic risks
  • Laparoscopic surgery converted during the operation to open surgery (laparotomy)
  • Leakage or failure of the anastomosis
  • Requirement for a stoma
  • Failure to remove the tumour
  • Change in bowel habit
  • Venous thromboembolism (DVT and PE)
  • Incisional hernias
  • Intra-abdominal adhesions
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19
Q

Right hemicolectomy

A

involves removal of the caecum, ascending and proximal transverse colon.

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20
Q

left hemicolectomy

A

involves removal of the distal transverse and descending colon.

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21
Q

High anterior resection

A

involves removing the sigmoid colon (may be called a sigmoid colectomy).

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22
Q

Low anterior resection

A

involves removing the sigmoid colon and upper rectum but sparing the lower rectum and anus.

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23
Q

Abdomino-perineal resection (APR)

A

involves removing the rectum and anus (plus or minus the sigmoid colon) and suturing over the anus. It leaves the patient with a permanent colostomy.

24
Q

Hartmann’s procedure

A

is usually an emergency procedure that involves the removal of the rectosigmoid colon and creation of an colostomy. The rectal stump is sutured closed. The colostomy may be permanent or reversed at a later date.

Common indications are acute obstruction by a tumour, or significant diverticular disease.

25
Q

Hartmann’s procedure

A

is usually an emergency procedure that involves the removal of the rectosigmoid colon and creation of an colostomy. The rectal stump is sutured closed. The colostomy may be permanent or reversed at a later date.

Common indications are acute obstruction by a tumour, or significant diverticular disease.

26
Q

Low Anterior Resection Syndrome

A

Low anterior resection syndrome may occur after resection of a portion of bowel from the rectum, with anastomosis between the colon and rectum. It can result in a number of symptoms, including:
* Urgency and frequency of bowel movements
* Faecal incontinence
* Difficulty controlling flatulence

27
Q

Follow-Up for colorectal cancer

A

Patients will be followed up for a period of time (e.g., 3 years) following curative surgery. This includes:
* Serum carcinoembryonic antigen (CEA)
* CT thorax, abdomen and pelvis

28
Q

Stomach (gastric) cancer background

A
  • 5th most common cancer globally
  • Presents with advanced disease
  • Majority of gastric cancers arise from gastric mucosa as adenocarcinomas.
  • The rest are a mixture of connective tissue, lymphoid or neuroendocrine malignancies
29
Q

RF for gastric cancer

A

rate has improved in the west due to H.pylori eradication therapy and improved diet
- H.pylori
- Male
- Age
- Smoking
- Alcohol
- Positive family history
- Pernicious anaemia

30
Q

presentation of gastric cancer

A
  • Vague and non-specific – pts present at advanced stage
  • Dyspepsia
  • Dysphagia
  • Early satiety
  • Vomiting (haematemesis
  • Melaena

Non-specific cancer SYMPTOMS
- ANOREXIA
- WEIGHT LOSS
- ANAEMIA

  • Clinical signs usually absent
  • Epigastric mass in late disease
  • Troisiers sign- palpable left supraclavicular node (Virchow node)- metastatic abdominal malignancy

Metastatic signs
- Hepatomegaly
- Ascites
- Jaundice
- Acanthosis nigricans (hyper pigmentation of skin creases e.g. axilla)

31
Q

sign assoicated with gastric cancer

A

palpable left supraclavicular node (Virchow node)- metastatic abdominal malignancy

32
Q

investigations for gastric cancer

A

Bloods: FBC, LFT

Imaging
- Urgent upper GI endoscopy (OGD) with biopsy- any patients presenting with new-onset dysphagia or aged >55 years presenting with weight loss and either upper abdominal pain, reflux, or dyspepsia.- signet ring cells
- CT may show thickening of gastric wall but does not allow direct visualisation or biopsy hence OGD

Biopsy
- Histology- neoplasia classification and grading
- CLO test- H.pylori
- HER2/neu protein expression (targeted monoclonal therapies)

Staging- CT chest-abdomen-pelvis and staging laparoscopy (looking for peritoneal metastases)- TNM staging

33
Q

Management of gastric cancer

A
  • MDT approach
  • Adequate nutrition e.g. NG, RIG may be needed

Curative treatment: surgery
- Peri-operative chemotherapy
- 3 cycles neoadjuvant and 3 cycles adjuvant

  • Palliative care
34
Q

Endoscopic Mucosal Resection (EMR)

A
  • Patients with early T1a tumours (tumours confined to the muscularis mucosa) may be offered an Endoscopic Mucosal Resection (EMR). This has the advantage of a greatly reduced morbidity, mortality, and quality of life impact, however is only used in early tumours therefore current use in clinical practice is rare.
35
Q

surgery for gastric cancer

A

Gastrectomy
The aim of surgery is to achieve loco-regional control by removing the tumour and its local lymph nodes. The type of operation performed depends on the region of the malignancy:
* Proximal gastric cancers – total gastrectomy
* Distal gastric cancers (antrum or pylorus) – subtotal gastrectomy

36
Q

reconstruction after gastrectomy

A

Roux-en-Y reconstruction
gives the best functional result, in particular with less bile reflux.
- Post-gastrectomy, distal oesophagus is end-to-end anastomosed directly to the small bowel, and the proximal small bowel is end-to-side anastomosed also to the small bowel

37
Q

Palliative management of gastric cancer

A

Most patients will be offered only a palliative approach due to the extent of disease at time of presentation. This may include :
- Chemotherapy
- Best supportive care
- Stenting (for patients who have gastric outlet obstruction secondary to an obstructing cancer).

**Palliative surgery **(usually distal gastrectomy or bypass surgery (a gastro-jejunostomy)) can be used when stenting fails or is not available. It can also be used cautiously in the palliation of bleeding gastric tumours.

38
Q

pancreatic cancer background

A
  • 4th most common cause of cancer-related deaths
  • Rare in <40s
  • Diagnosed late and very poor prognosis due to late presentation
39
Q

types of pancreatic cancer

A

vast majority adenocarcinomas

Ductal carcinoma (most common)
- From exocrine portion

Pancreatic cystic carcinoma
- From exocrine protion

Endocrine tumours
Derived from islet cells of the pancreas (better prognosis)

40
Q

Location of pancreatic cancer

A
  • Most occur in head of pancreas (as opposed to body or tail)
  • Once large enough will press on bile duct- obstructive jaundice
  • Tumours located in the body and tail are diagnosed later due to obstructive symptoms occurring later
41
Q

metastasis in pancreatic cancer

A

Metastasis (early)
- Liver
- Peritoneum
- Lungs
- Bones

42
Q

Risk factors for pancreatic cancer

A
  • Age (60-80)
  • Male
  • Smoking
  • Obesity, diet (red meat, low fruit), alcohol
  • Diabetes
  • Fx
43
Q

presentation of pancreatic cancer

A

RED FLAG: Painless obstructive jaundice is a key presenting feature that should make you immediately consider pancreatic cancer (the key differential is cholangiocarcinoma)
* Yellow skin and sclera
* Pale stools
* Dark urine
* Generalised itching

The other presenting features for pancreatic cancer can be vague:
* Non-specific upper abdominal or back pain
* Unintentional weight loss
* Palpable mass in the epigastric region
* Change in bowel habit
* Nausea or vomiting
* New onset diabetes or worsening of type 2 diabetes

44
Q

examination findings of someone with pancreatici cancer

A
  • Cachetic, malnourished, jaundiced
  • Abdominal mass in epigastric region
45
Q

pancreatic cancer investigations

A

Initial bloods
- FBC and LFTs

CA 19-9 (carbohydrate antigen) is a tumour maker raised in pancreatic cancer (also raised in cholangiocarcinoma)

Imaging
- Abdominal US
- Staging CT- CT TAP (Looks for metastasis and other cancers)
- Magnetic resonance cholangial pancreatography (MRCP)- assess biliary system
- Endoscopic retrograde cholangial-pancreatography (ERCP)- stent to relieve obstruction and biopsy tumour
- Endoscopic US for staging

Biopsy
- Through skin under US OR CT guidance

46
Q

refferal for pancreatic cancer

A

Referral
* Over 40 with jaundice – referred on a 2 week wait referral
* Over 60 with weight loss plus an additional symptom (see below) – referred for a direct access CT abdomen

The NICE guidelines suggest a GP referral for a direct access CT abdomen (or ultrasound if not available) to assess for pancreatic cancer if a patient has weight loss plus any of:
* Diarrhoea
* Back pain
* Abdominal pain
* Nausea
* Vomiting
* Constipation

47
Q

management of pancreatic cancer

A
  • HPB MDT meeting
  • Surgery
  • Palliative
48
Q

surgery for pancreatic cancer

A
  • Only curative procedure is radical resection (only 20% have resectable tumours)
  • More likely to be considered with small tumours isolated in the head of the pancreas
    –> Total pancreatectomy
    –> Distal pancreatectomy
    –>Pylorus-preserving pancreaticoduodenectomy (PPPD) (modified Whipple procedure)
    –>Radical pancreaticoduodenectomy (Whipple procedure)

Adjuvant chemotherapy e.g. gemcitabine or 5-fluorouracil (5-FU)

49
Q

whipples procedure

A

A Whipple procedure (pancreaticoduodenectomy) is a surgical operation to remove a tumour of the head of the pancreas that has not spread. A Whipple procedure is a massive operation so patients need to be in good baseline health. It involves the removal of the:

  • Head of the pancreas
  • Pylorus of the stomach
  • Duodenum
  • Gallbladder
  • Bile duct
  • Relevant lymph nodes
50
Q

Prognosis of pancreatic cancer

A
  • 6 months from diagnosis
  • High metastatic capacity even in small tumours
  • 5 year survival of 10%
51
Q

named signs for pancreatic cancer/ cholangiocarcinoma

A
  • Courvoisiers law
  • Trousseaus sign of malignancy
52
Q

Courvoisier’s law

A

states that a palpable, painless gallbladder along with jaundice is unlikely to be gallstones.

The cause is usually cholangiocarcinoma or pancreatic cancer

53
Q

Trousseau’s sign of malignancy

A

refers to migratory thrombophlebitis as a sign of malignancy, particularly pancreatic adenocarcinoma.
- Thrombophlebitis is where blood vessels become inflamed with an associated blood clot (thrombus) in that area.
- Migratory refers to the thrombophlebitis reoccurring in different locations over time.

54
Q

management of secondary liver cancer

A

Management
- Due to nature of metastasis surgery is more diff and less useful- resection not particularly useful
- Surgery may be considered if metastasis confined to the liver and the primary tumour is under control
- Oncological and palliative input important
- Alternatives
o Transarterial chemoembolization
o Selective interval radiotherapy

55
Q

carcinoid colon cancer

A

Gastrointestinal (GI) neuroendocrine tumors (also called gastrointestinal carcinoid tumors) form from a certain type of neuroendocrine cell (a type of cell that is like a nerve cell and a hormone-making cell). These cells are scattered throughout the chest and abdomen but most are found in the GI tract.

presentation
* a tumour in the bowel may cause tummy pain, a blocked bowel (diarrhoea, constipation, feeling sick or being sick) and bleeding from the bottom (rectal bleeding)
* Facial flushing
* a tumour in the lung may cause a cough, which may make you cough up blood, and cause wheezing, shortness of breath, chest pain and tiredness
* a tumour in the stomach may cause pain, weight loss, tiredness and weakness