Biliary Tract Disease* Flashcards

1
Q

What is the anatomy of the biliary tree? (10 key steps to remember)

A

1) Intrahepatic bile ducts, drain bile from the hepatocytes into
2) L and R hepatic duct, drain bile into
3) Common hepatic duct, drains bile into
4) Cystic duct, a two way duct which is connected to the
5) Gall bladder, a sac used to store bile and contract to release it once stimulated by leptin release in the stomach upon eating fatty foods. This releases bile back into 4, which drains into
6) Common bile duct, which joins the,
7) Pancreatic duct, responsible for draining pancreatic enzymes amylase/lipase/trypsinogen etc. Together they join in a space called
8) Ampulla of Vater, which opens via the
9) Sphincter of Oddi into
10) 2nd part of the duodenum

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2
Q

What is the epidemiology and risk factors for gall stones?

A

One of the most common admissions to general surgeons
- Multiple different presentations

Risk factors:
- ‘fat fair fertile female forty’ = BMI >30, Caucasian, 1+ children = typical demographic
SOLID:
- Sudden weight loss (rapid fat metabolism = liver secretes extra cholesterol into bile = stones)
- OCP (progesterone + oestrogen effects)
- Loss of bile salts (i.e. following ileal resection, terminal ileitis - from Crohn’s - pigment/oxalate stones)
- Increasing age
- Diabetes

Smoking

(Crohn’s gives you Stones)

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3
Q

What is the pathophysiology of gallstones?

A

Bile contents:

  • Water
  • Bile salts (facilitate digestion of fats/oils by forming micelle-based surfactants)
  • Bile pigments (Bilirubin + biliverdin - from Hb degeneration)
  • Cholesterol and phospholipids

Stone types:

  • Cholesterol stones = most common, large, often solitary
  • Pigment stones = small, irregular
  • Mixed stones = least common (cholesterol + pigments)
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4
Q

How can gallstones present?

A

1) Asymptomatic
- Very common incidental finding on scans
2) Biliary colic
3) Cholecystitis
4) Ascending cholangitis
(+biliary sepsis)
5) Pancreatitis
6) Gall stone ileus

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5
Q

What is biliary colic and how does it present?

A

Gall stone temporarily blocking the cystic duct

Colicky RUQ pain

  • Lasting 15-60+mins
  • Often occurring after a heavy fatty/greasy meal or during the night
  • Repeated attacks are common
  • May radiate to the R shoulder
  • Possible N+V
  • Normal vital signs
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6
Q

What is cholecystitis and how does it present?

A

Gall stone lodged in the cystic duct (or CBD) leading to gall bladder inflammation and swelling

Constant RUQ pain

  • More painful than colic
  • Lasting longer than colic
  • Again possibly triggered initially by fatty/greasy meal or during the night
  • May radiate to R shoulder
  • N+V very common
  • Fever is also common
  • Triad:
  • Murphy’s sign +ve
  • Possible mild jaundice (if CBD (partial) obstruction)
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7
Q

What is ascending cholangitis and how does it present?

A

Inflammation of the bile ducts as a result of an ascending infection from bacteria (E.coli*, Klebsiella spp., Enterococcus) in the the duodenum, often in the context of a partial/complete blockage of the biliary tree (often the CBD) by a gallstone
- May also happen if biliary strictures or tumour compression

Presents in the same way as cholecystitis/in a person with known stones

  • RUQ pain + fever/rigors + jaundice = Charcot’s triad
  • ” + septic shock + confusion = Reynold’s pentad

A medical emergency

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8
Q

What is gallstone pancreatitis?

A

Blockage of the pancreatic duct with a gall stone leading to back pressure within the duct and inflammation

FOR MORE CARDS SEE PANCREATITIS DECK

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9
Q

What is gallstone ileus and how does it present?

A

Not directly a gallbladder problem, nor a true ileus

Chronic gallstone in gall bladder > rubbing between duodenum and gall bladder > fistula formation > stone into small bowel lumen > passage until the next point of narrowing = ileocecal valve > obstruction

Presents like an obstruction
- SEE OBSTRUCTION DECK

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10
Q

What blood tests are useful in biliary disease?

A

WCC:

  • Colic = normal
  • Acute cholecystitis = +
  • Acute cholangitis = +++

Bilirubin:

  • (>50-may also complain of itching)
  • Colic = normal
  • Acute cholecystitis = +
  • Acute cholangitis = +++

ALP:

  • Colic = +
  • Acute cholecystitis = ++
  • Acute cholangitis = +++

Blood cultures in cholangitis

Lipids:
- Might be useful

Amylase/lipase:
- To rule in/out pancreatitis

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11
Q

What role do USS and XR play in investigating biliary disease?

A

USS

  • Best first line - can spot 90+% of stones, measure CBD diameter (dilated in obstruction)
  • Thickened GB wall >3mm in cholecystitis

A/CXR
- Not first line as not all stones are radiolucent cholesterol stones above a certain size are however - may stones are found incidentally in this manner

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12
Q

What special tests are used in biliary disease?

A

MRCP

  • Magnetic retrograde cholangiopancreatography
  • MR of the biliary tree

ERCP
- Endoscopic retrograde cholangiopancreatography - for diagnosis in absence of positive USS findings and for therapeutic extraction

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13
Q

What management is needed for biliary colic, cholecystitis and cholangitis?

A

Analgesia:

  • Paracetamol +/- NSAIDs (incl. PR diclofenac) +/- opiates
  • Often parentral as may be N+V

Antibiotics:

  • For cholecystitis
  • IV Abx e.g. co-amox + metronidazole

Lifestyle factor modification advice

Laparoscopic cholecystectomy +/- open conversion
- Indicated within 1wk of presentation of acute cholecystitis; can be done elective for cholelithiasis

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14
Q

What is aclaculus cholecystitis?

A

Cholecystitis picture that result from biliary stasis and/or gallbladder ischaemia

Aetiology:

  • severe tissue in jury, including post-op
  • DM
  • Malignancy
  • CCF, cardiac arrest, shock

Managed in the same way

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15
Q

What is primary biliary cholangiti/cirrhosis?

A

Progressive, autoimmune condition involving the destruction of interlobular bile ducts
- Subsequent intrahepatic cholestasis, cell damage, fibrosis and eventually cirrhosis

Aetiology
- Unknown, multifactorial; FHx strong

Rare:

  • 35/100,000
  • F>M at 10:1
  • Median age of onset 65yrs
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16
Q

How does PBC present?

A

25% of diagnoses are incidental due other bloods taken at the time

Should be suspected where chronic cholestasis is found after excluding other liver disease

Fatigue and pruritis = most common symptoms

RUQ pain/discomfort

Jaundice with dark urine and pale stool

Hepatomegaly, hyperpigmentation

Sjogren’s syndrome - common co-incidence
- also thyroid disease, CREST, coeliac, HCC, sero+ve/-ve arthritis’, gallstones, osteoporosis, hyperlipidaemia

Signs of liver cirrhosis in later stages

17
Q

What do investigations show in PBC?

A

ESR - raised

LFTs - ALP raised, bilirubin rises with disease progression

IgM - raised

Autoantibodies are characteristic:

  • Antimicrobial Abs = >90% - most significant
  • ANA
  • Other autoAbs e.g. to thyroid

TFTs

Fibroscan (for degree of fibrosis)

18
Q

How do you manage PBC?

A

No treatments are very effective but may help symptoms

Ursodeoxycholic acid

  • Immunomodulatory effect
  • Also reduces cholesterol absorption and is used to dissolve cholesterol gallstones

Modafinil
- for fatigue

Colestyramine
- Bile sequesterant

Liver transplant = only cure (but can recur in transplant)

ADEK supplementation

Avoid oestrogen containing drugs

19
Q

What is primary sclerosing cholangitis?

A

Chronic cholestatic disorder resulting from inflammation and fibrosis of intra- and extrahepatic bile ducts

Aetiology unknown

M>F, median age 35yrs

Significant association with IBD, notably UC

20
Q

How does PSC present?

A

Asymptomatic and incidental

Jaundice, pruritis

RUQ pain, hepatomegaly

Fever, weight loss, sweats

21
Q

How do you investigate PSC and what are the findings?

A

LFT:

  • ALP and GGT raised
  • transaminases normal or elevated
  • Bili = raised in advanced

Perineutrophil cytoplasmic antibodies (p-ANCA), antocardiolipin (aCL) and ANA

IgG and IgM

Hypergammaglobulinaemia

USS + MRCP

Biopsy for histological staging

22
Q

How do you manage PSC?

A

Drugs dont really improve mortality or morbidity; transplant remains only cure

Ursodeoxycholic acid
- May slow progression

Colestyramine - for pruritis

ADEK supplementation

Increased risk of cholangiocarcinoma and colorectal cancer - colonoscopy indicated

23
Q

What are the 3 main differences between PBC and PSC?

A

Sclerosis of bile ducts:

  • PBC = small interlobular
  • PSC = intra and extra-hepatic ducts

Sex:

  • PBC = F
  • PSC = M

Associations:

  • PBC = AMA Abs
  • PSC = UC/IBD