Biliary strictures
Appearance
Workup for cholestatic pattern, with suspected stricture
[edit | edit source]- USS
- MRI (CT considered better by some for distal duct obstruction)
- FBE, CA19-9, CEA, IgG, IgG4, HIV
- If still no clear cause, probably going to need ERCP
Benign biliary strictures - end result of either traumatic injury or inflammatory processes.
[edit | edit source]Iatrogenic injury (most common cause)
[edit | edit source]- Usually cholecystectomy - see 'cholecystectomy' page for how to avoid, and classification (Strasberg)
- Management
- PTC and downstream dilatation
- Use an angioplasty balloon catheter then leave a transhepatic stent
- ERCP
- Hepaticojejunostomy with transanastamotic stent, which stay in for 2-3 months
- PTC and downstream dilatation
- Specific situations
- Strasberg A - ERCP and biliary stent placement
- Strasberg B or C - often do not require operative intervention, but if they get recurrent sepsis/cholangitis, a right posterior hepatic sectionectomy is typically the best option
- Strasberg D - variable - endoscopic vs IR dilation and stenting. Primary end to end will likely fail if it's a thermal injury due to fibrosis and retraction, so excising a portion of the duct and performing hepaticojejunostomy may be necessary.
- Strasberg E - always requires biliary-enteric reconstruction
- Management
PSC
[edit | edit source]- See separate topic
Recurrent pyogenic cholangitis
[edit | edit source]- A syndrome of repeated attacks of cholangitis secondary to biliary stones and strictures that involve the extra- and intra-hepatic ducts
- Also known as oriental cholangiohepatitis or hepatolithiasis
- Epidemiology
- Almost exclusively seen in Asians (in Asia and diaspora)
- Men and women equal
- Most commonly strikes at 20-40yo in lower SES
- Aetiology
- Unknown
- Pathophysiology
- Stones and strictures develop in the biliary tree, but not known which occurs first
- Stones are bilirubinate stones
- Association with Clonorchis sinensis and Ascaris lumbricoides
- Strictures usually involve the intrahepatic main hepatic ducts, most often the left hepatic duct
- GB can be involved (20%)
- Complications
- Cirrhosis can develop secondary to strictures
- Choledochoduodenal fistula
- Acute pancreatitis
- Increased incidence of cholangiocarcinoma
- Presentation
- Repeated bouts of cholangitis
- Diagnosis
- Favoured if there are multiple ductal stones, abscesses
- Use combination of USS, CT and ERCP
- Treatment
- Acute
- A syndrome of repeated attacks of cholangitis secondary to biliary stones and strictures that involve the extra- and intra-hepatic ducts
- Focus on decompression
- Surgical has historically been favoured - open CBD exploration or endoscopic papillotomy with stenting
- PTC reserved for poor-risk surgical patients
- Chronic
- Surgery is often indicated
- Hepatic resection if it's within an isolated segment (for intra-hepatic strictures, hepatic atrophy, liver abscess, or suspicion of cholangiocarcinoma)
- All the way through to liver transplant
IgG4-related sclerosing cholangitis
[edit | edit source]- A/w AIP
- Most frequently presents as painless obstructive jaundice
- Most widely-used diagnostic criteria are HISORt
Ischaemic cholangiopathy
[edit | edit source]AIDS-associated cholangiopathy
[edit | edit source]Secondary sclerosing cholangitis in critically ill patients
[edit | edit source]Acute/chronic pancreatitis
[edit | edit source]- Pancreatic fibrosis results in distal biliary strictures involving the entire intra-pancreatic portion of CBD and causing proximal dilation
- Serum ALP is most sensitive marker
- Diagnosed on MRCP or ERCP (long, smooth, gradual tapering of distal CBD)
- Need to exclude periampullary tumour
- Treatment:
- Most commonly biliary bypass - either choledochodeodenostomy or choledochojejunostomy
- If malignancy can't be excluded, or chronic pain is a feature, pancreaticoduodenectomy is possible
- Endoscopic therapy is generally not as good - can be trialled, but guidelines say if it's ineffective after 12 months, need surgery/hypass
Autoimmune pancreatitis
[edit | edit source]- Rare inflammatory disease almost uniformly responsive to steroids
- Often have obstructive jaundice and pancreatic mass
- Types
- Type I - IgG4-related, relapsing, not limited to pancreas
- Type II - limited to pancreas, rarely relapsing
Post-surgical biliary strictures
[edit | edit source]- Post-cholecystectomy
- Post-liver transplantation
Malignant
[edit | edit source]- Pancreatic cancer
- CA19-9 is best tumour marker, but can also do CEA
- Cholangiocarcinoma
Features that support malignancy:
- Long-segment
- Irregular
- Early enhancement
- Associated soft tissue mass
- Direct invasion/infiltrative features
- DWI