Biliary System Flashcards

1
Q

Contraindications of Cholecystectomy

A
  • Acute cholecystitis if present for more than 72 hours
  • Cholangitis
  • Peritonitis
  • sepsis
  • Pancreatitis
    • after pancreatitis has resolved, laparoscopic cholecystectomy is indicated to prevent future pancreatitis.
  • Bowel distension
  • Portal hypertension
  • Morbid obesity
  • GB Cancer
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2
Q

what are the locations of this disease?

A
  • Cholangiocarcinoma
    • Hilar
      • originates from epithlium of main hepatic ducts or junction
      • KLATSKIN TUMOUR (image)
    • peripheral
      • originates from the epithlium of intralobular ducts
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3
Q

Von meyenburg Complex

A
  • AKA bile duct hamartoma/adenoma
    • Benign tumour composed of disorganised bile ducts and ductules and fibrocollagenous stroma.
  • usually small 1-5mm
  • however the nodules may coalesce into larger masses.
  • Bile duct hamartoma is benign, however, there have been reports of an association of cholangioca with multiple bile duct hamartomas
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4
Q

Types of biliary enteric fistulae

A
  • Biliary gastric
  • biliary duodenal - most common, may cause gallstone ileus
  • biliary-colonic
  • Bouveret syndrome: obstruction of stomach or duodenum by stone
  • Iatrogenic
    • ERCP, Surgical
    • most common cause for biliary ductal gas
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5
Q

What is this?

Two types?

A
  • Cholangiocarcinoma
  • adenocarcinoma of the biliary tree
  • Two types
    • scirrhous type
      • worse prognosis
    • Polypoid type
  • Clincal
    • jaundice
    • pruritus
    • weigh loss
  • Rx
    • pancreaticodyodenecticomy (whipples)
    • palliative procedures
      • stent
      • biliary bypass
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6
Q

what is this?

A

Biliary cystadenoma

  • uncommon, multilocular cystic liver mass that originates in the bile duct and usually occurs in the right hepatic lobe.
  • Typically occurs in women
  • h/o chronic abdominal pain
  • it may represent a congenital anomaly of the biliary anlage
  • COMPLICATIONS
    • Malignant transformation cystadenocarcinoma occurs
  • IMAGING FEATURES
    • well defined and cystic
    • internal sepations
    • The cyst walls and any other soft tissue components typically enhance with contrast
    • variable appearance on MRI depending on the protein content of the fluid and the presence of an intracystic soft tissue component.
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7
Q

Name 3 cystic diseases of the biliary tract

A
  1. Choledochal cyst: cyst in the main duct
  2. Choledochocele: cysts in the main duct at the duodenal opening
  3. Caroli Disease: Cysts in the small biliary branches within the liver
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8
Q

What is MRCP

A
  • Fat sat T2 imagines of the upper abdo
  • bile is hyper intense
  • images of the biliary and pancreatic ducts can be rendered by maximum signal intensity projection recons (MIPS)
  • Common indications
    • unsuccessful ERCP
    • ERCP contraindicated
    • biliary-enteric anastomoses
      • chledochojejunostomy
      • billroth II
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9
Q

How common are biliary cancers?

A

Bilary cancers (adenocarcinoma and cholangiocarcinoma) are the 5th most common GI malignancy

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10
Q

What are the Imaging features of Sclerosing Cholangitis?

A
  • Irregular dilatation
  • stenosis
  • beading of intrahepatic and extrahepatic bile ducts (seen best on cholangiogram)
  • string of beads appearance
  • small ‘diverticula’ of biliary tree are PATHOGNOMONIC
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11
Q

What is this?

A

Adenomyomatosis

  • most comon form of hyperplastic cholesterolosis
  • marked hyperplasia of the GB wall
  • Epithelium herniates into the wall
  • forms rokitansky-Aschoff sinuses
  • May be focal or diffuse
  • IMAGING FINDINGS
    • Rokitansky-Ashkoff sinues
      • hypoechoic if contain bile
      • hyperechoic if contain sludge or calculi
    • High amplitude foic in the wall (cholesterol crystals) that produce comet tail artifacts (V shpaed ring down artifacts)
    • Thickening of GB wall is common but non specific
    • inflammation is not typical
    • hypercontractility
  • MRI
    • Rokitansky-aschoff sinuses
      • T1 hypo
      • T2 hyper
      • non enhancing
    • Thickening of GB wall Nonspecific
    • Inflammation is not typical
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12
Q

Imaging Features for Acalculus Cholecystitis

A
  • No calc
  • sludge and debris
  • usually in critically ill patients
  • same findings as calculous cholecystitis
    • Murphys positive
    • GB wall thickening
    • Pericholecystic fluid
    • GB distension
  • Hepatic iminodiacetic acid derivative (HIDA) scanning:
    • non visualisation of the GB
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13
Q

Name the Ductal anatomy

A
  • Right Hepatic duct
    • Right Anterior superior
    • Right anterior inferior
    • Right posterior superior
    • right posterior inferior
    • Caudate
  • left hepatic duct
    • left medial superior segment
    • left lateral superior
    • left medial inferior
    • left lateral inferior
  • the RHD and the LHD form the common hepatic duct (CHD) which receives the cystic duct from the GB to form the CBD.
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14
Q

What are the DDx of Sclerosing cholangitis?

3

A
  • Primary biliary cirrhosis
    • normal extrahepatic ducts
  • AIDS cholangiopathy
    • may be a/w ampullary stenosis
  • Sclerosing cholangiocarcinoma
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15
Q

whis is this?

what are the types and causes?

A

sclerosing cholangitis

  • Chronic inflammatory process of intrahepatic 20% and extrahepatic 80% bile ducts that causes progressive narrowing.
  • Chronic or intermittent obstructive jaundice is evident.
  • Types
    • Primary (idiopathic)
    • Secondary
      • IBD (usually UC) 65%
      • Cirrhosis
      • chronic active hepatitis
      • Retroperitoneal fibrosis
      • Pancreaittis
      • Riedel thyroiditis
      • peyronie disease
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16
Q

Imaging findings of Intrahepatic Cholangiocarcinoma

where geographically is it more common?

A
  • More common in asia than in the USA
  • Adenocarcinoma from the intrahepatic bile ducts
  • Biliary ductal dilatation distal to tumour
  • lesions have irregular borders with infiltrative margins
  • Delayed peripheral to central enhancement as a result of fibrosis and hypovascularity
  • Capsular retraction and vascular invasion.
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17
Q

ERCP/MRCP finding:

Smooth, thick wall, can have a short or long stricture

Association: 1

A

Autoimmune cholangitis

A/W : autoimmune pancreatitis

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18
Q

What is recurrent pyogenic cholangitis?

which lobes of the liver are most effected?

A

recurrent pyogenic cholangitis

  • endemic disease in asia
  • recurrent fever, jaundice, abdo pain
  • Cuase
    • Clonorchis sinensis and
    • Ascaris
    • bacterial super infection
  • COmmon in asia, young adults
  • imaging features
    • Biliary dilatation
      • extra and intra
      • Left lobe and posterior irhgt lobe most common
    • biliary strictures
    • Intrahepatic calculi
      • hepatolithiasis
        • contains calcium biilirubinate, cellular debris and mucinous substance
        • Typically hyperechoic and casts shaddows
        • stones may not be sufficiatnely hyper dense to be detectable by CT
  • Complications
    • intrahepatic abscess formation
    • hepatic atrophy as a result of PV occlusion
    • Cholangioca.
    • PD involvement
    • GB disease in 20%
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19
Q

Complications of cholecystectomy

what is this called?

A
  • 0.5-5%
  • biliary obstrction
    • clipping or thermal injury to CBD
    • Postoperative fibrosis
    • usually requires percutaneous drainage
  • Biliary leak causing peritonitis and/or biloma
    • CD stump leak,
    • injury to CBD,
    • leak from small luschka bile ducts draining directly in GB
  • Detection of bile leaks
    • HIDA scan
    • ERCP
    • Transhepatic cholangiogram
    • MR with heaptobiliary contrast
  • Other
    • retained stones
    • stones dropped in peritoneal cavity (Morison Pouch)
    • Bowel perforation
    • Hemorrhage
    • infection
  • The bile ducts of Luschka, or subvesical ducts, are small ducts which originate from the right hepatic lobe, course along the gallbladder fossa, and usually drain in the extrahepatic bile ducts. Injuries to these ducts are the second most frequent cause of postcholecystectomy bile leaks
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20
Q

Caroli disease

A
  • Segmental cystic dilation of intrahepatic (only) bile ducts
  • ie the type 5 subset of choledochal cysts
  • Cause unknown
  • autosomal recessive
  • Sequence of events
    • bile stasis predisposes to intrahepatic calculi
    • secondary pyogenic cholangitis
    • intrahepatic abscesses
    • increased risk of cholangiocarcinoma
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21
Q

describe the location of the HA relative to the CBD

A
  • Most common 80%
    • HA is between the CBD and the PV
    • HA medial to the main PV and
    • CBD lateral to the PV
  • Less common 20%
    • HA anterior to CBD
    • HA posterior to PV
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22
Q

ERCP/MRCP finding:

Smoothly narrowed biliary duct, even with stricture

RFs: 2

A

benign stricture

Risk factors:

recurrent cholangitis

surgical intervention

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23
Q

What are the associations of GB carcinoma?

5

A
  1. Cholelithiasis 90%
  2. IBD (UC > CD)
  3. Porcelain GB 1%
  4. familial polyposis
  5. Chronic cholecystisis
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24
Q

where is the CHD measured on US?

What are the normal measurements?

A
  • CHD measurements (inner wall to inner wall) are performed at the level of the hepatic artery
  • Normal measurements
    • <7mm in normal fasting patients <60yo
    • <10 mm in normal fasting patients >60yo
    • <11mm in pts with previous
      • surgery
      • CBD obstruction
  • Fatty meal challenge
    • if CHD enlarges more than 2mm after fatty meal, it indicates obstruciton
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25
Q

Complications of Cholecystitis

what is this?

A
  • Gangrenous cholecystitis
    • rupture of GB
    • mortality 20%
    • Gangrene causes nerve death so that 65% of pts have a negative murphy sign.
  • Emphysematous cholecysitis
    • rare
    • 40% occur in diabetics
  • Empyema

https://radiopaedia.org/cases/gangrenous-cholecystitis-3

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26
Q

what is this?

what are the complications?

A
  • xanthogranulomatous cholecystitis
    • women begtween 60-70
    • RUQ pain
    • vomiting leukocytosis
    • Postive Murphies
    • Gallstones
    • marked thickening of GB wall
    • Inflammatory changes in contiguous hepatic parenchyma
    • difficult to differentiation from adenocarcinoma
  • Complications
    • perforation
    • abscess formation
    • fistulous tracts to the duodenum or skin
    • extension of the inflammatory process to the liver, colon or surrounding soft tissues
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27
Q

US features of Gall stones

what sign is this?

A
  • posterior shaddow.
    • very small stones may not shadow, reposition the patient to heap up calculi
  • Mobility of stones
    • gravity dependant movememnt
    • stones impacted in the neck or stones adherent to the wall will not move
  • Wall-echo-shaddow (WES triad, double arc sign) is seen if the GB is contracted (type II) and completely filled with stones
  • WES can also be seen with
    • porcelain GB
    • emphysematous cholecystitis
  • highly reflective echo originating from the anterior surface of the calculus
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28
Q

What conditions are a/w this tumour?

A

cholangiocarcinoma associations

  • Image = klatskin tumour
  • ASSCIATIONS
    • UC
    • Chlonorchis exposure in Asian population
    • Caroli Disease
    • Benzene and toluene exposure
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29
Q

Bismuth classification of bile duct injury

name the types

A
  • Based on the level of traumatic injury in relation to the confluence of the LHD and the RHD
    • type 1: Injury >2cm distal to the confluence
    • type 2: injury < 2cm distal to confluence
    • Type 3: Injury immediately distal to confluence but with intact confluence
    • Type 4: A destroyed confluence
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30
Q

Causes and Imaging features of Acute Cholecystitis

A
  • Gallstone obstruction 95%
  • Acalculous cholecystitis 5%
  • USS features
    • Luminal distension > 4cm
    • Wall thickening > 5mm edema, congestion
    • thickening is usually worse on the hepatic side
    • Gall stones
    • Cystic duct stones may be difficult to detect if they are not surrounded by bile
    • +ve murphy sign
    • pericholecystivc fluid
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31
Q

Name variations of papillary insertion

A
  • Ducts within Papillar = ampulla
  • the CBD drains into the duodenum through the ampula
    • Y type
      • CBD and pancreatic duct combine before insertion into ampulla
      • 75%
    • V type
      • CBD and PD insert jointly into ampulla
      • 25%
    • U type
      • CBD and PD insert separately into ampulla
      • 5%
    • long common channel:
      • CBD and PD merge > 1.5cm proximal to ampulla
      • increased risk of biliary tract ca.
32
Q

GB Adenoma

A
  • single
  • multiple 10%
  • 5-20mm
  • 60% a/w cholelithiasis
  • found in 0.5% of cholecystectomy patients (F > M)
  • more common in
    • peutz-jeghers
    • familial adenomatous polyposis
  • Polys >1cm require a careful search for features a/w malignancy
    • thickening or nodularity of the GB wall
    • evidence of hepatic invasion
      • indistinct margin between liver and GB
    • bilary duct dilatation
    • peripancreatic or hepatoduodenal ligament adenopathy
  • GB adenomas are usually smoothly marginated.
  • Intraluminal polyploid masse should raise concern for malignancy
  • homogeneously hyper echoic
  • Can be difficult to distinguish from non calcified gall stones.

Pathology

A wide variety of entities appear as polyps and histology is variable:

  • benign polyps: 95% of all polyps
    • cholesterol polyps: >50% of all polyps 3,7,14
    • adenoma: ~30%, possibly premalignant 4
    • inflammatory polyps: ~10% 14
    • other rare entities (see benign tumours and tumour-like lesions of the gallbladder)
  • malignant polyps: 5% of all polyps
    • adenocarcinoma: ~90% of malignant polyps
    • other rare entities including
    • metastases to gallbladder
    • squamous cell carcinoma
    • angiosarcoma
  • Case Discussion

The management and follow-up of gallbladder polyps is controversial and practice varies between centres. However, due to the increased risk of malignancy, polyps measuring 10mm or greater should be considered for cholecystectomy 1.

This patient underwent cholecystectomy and a gallbladder adenoma with low-grade dysplasia was confirmed by histopathology.

33
Q

What are the imaging features of GB cancer?

A
  • Intraluminal soft tissue density
    • polypoid
    • fungating
  • asymmetrically thickened GB wall
  • Usually no bilary dilatation
  • Cholelithiasis
  • Direct invasion of liver
    • direct extension 50%
    • distant liver mets 5%
  • Gastrohepatic and hepatoduodenal ligaments
    • ligamentous extension 75%
    • direct invasion into duodenum 50%
    • LN mets 70%
  • LN’s
    • Foramen of winslow node
    • superior and posterior pancreaticoduodenal nodes
    • hepatic and celiac nodes
    • peritoneal spread
    • carcinomatosis 50%
    • intestinal obstruction
34
Q

frequency of gall stones?

% of these that are calcified

% that are asymptomatic

A
  • 10-20% of pop have gallstones
  • 30% are calcified
  • 30-50% are asymptomatic
35
Q

what is this?

A

Mirizzi syndrome is a rare complication of gallstone disease in which a gallstone becomes impacted in the cystic duct or neck of the gallbladder causing compression of the common bile duct (CBD) or common hepatic duct, resulting in proximal obstruction.

The patient may present initially with colicky epigastric pain or manifest with hyperbilirubinaemia (jaundice).

The obstructive jaundice can be caused by direct extrinsic compression of CHD/CBD by the stone or from fibrosis of the same caused by chronic inflammation.

A cholecystocholedochal fistula can occur as a further complication to this condition if left untreated.

36
Q

Imaging features of Cholangiocarcinoma

A
  • Dilated intrahepatic ducts with normal extra hepatic ducts
  • hilar lesions
    • central obstruction
    • lesions are usually infiltrative so that a mass is not usually apparent
    • encasement of PVs causes irregular enhancement by CT
  • Peripheral lesions
    • may present as a focal mass or be diffusely infiltrative
    • retain contrast material on delayed scans
    • occasionally invade veins
  • ERCP patterns
    • short annular constricting lesion 70%
    • long stricture 10%
    • intraluminal polyploid mass 5%
37
Q

Ongoing Management post Cholecystostomy

A
  • if there is no cholelithiasis, the catheter is usually left for 3 weeks.
  • at this point, the catheter is clamped to make sure that there is adequate internal drainage.
  • if the patient tolerates clamping the catheter can be removed,
  • if there is cholecystitis, the catheter is left in place until the patient is stable and can undergo a surgical cholecystectomy
  • Unlike pts with acalulous cholecystitis, pts with cholelithiasis have an irritant in the GB and thus a reason for inflammation to recur.
38
Q

what is this?

A

Bilomas refer to extrabiliary collections of bile. They can be either intra- or extrahepatic.

Terminology

There is a slight discrepancy in the reported literature in the use of the term “biloma”. Many authors have used it exclusively to refer to intrahepatic bile collections or other bilious collections which are discretely organised rather than free biliary leak into the peritoneum (choleperitoneum: a rarely used term).

Clinical presentation

Although usually asymptomatic, they may present with symptomatic bile peritonitis 7.

Pathology

They can result from a number of causes:

spontaneous

trauma

postinstrumentation

transcatheter arterial chemoembolisation (TACE)

percutaneous ethanol injection

microwave ablation

percutaneous biliary drainage

post surgical, e.g. injury to duct of Luschka following cholecystectomy 6

Seventy percent of bilomas are localised to the right upper quadrant, whereas the remaining 30% develop in the left upper quadrant. A biloma may wall off or may continue to demonstrate active bile leakage.

39
Q

Imaging features of this condition

A

AKA bile duct hamartoma/adenoma

Von Meyenburg complex

  • Can simulate metastases or microabscesses
  • therefore histo dx is needed.
  • Multiple bile duct hamartomas may simulate mets or hepatic abscesses
  • small well-defined hypoattenuating or isoattenuating mass
  • little if any hancement
  • MRI:
    • usually hypo on T1 and
    • iso or hyper on T2
    • No enhancement post Gd
  • USS
    • hypoechoic lesions contained central echogenic focus with ring down artifact as a result of cholesterol crystals
40
Q

ERCP/MRCP finding:

Multifocal intrahepatic strictures and dilatations

RFs: 1

A

Primary sclerosing cholangitis

RFs: UC

41
Q

What is chemotherapy cholangitis?

what is the disease hallmark?

A
  • Iatrogenic cholangitis after intraarterial chemotherapy
  • ischaemic cholangiopathy
  • floxuridine has been used
  • strictures of CHD, frequently involving the biliary bifurcation
  • sparing of the distal CBD (disease Hallmark)
42
Q

what is this?

A
  • Choledocholithiasis
  • stone in the CBD
  • Typically a/w high grade obstection and jaundice
  • 75% diagnostic accuracy
43
Q

What are the advantages of MRCP over ERCP?

A
  1. non invasive
  2. cheaper
  3. no radiation
  4. no anesthesia
  5. less operator dependant
  6. allows better visualisation of the ducts proximal to obstruction
  7. allows for observation of extraductal disease
44
Q

Describe the steps of a Cholecystostomy

A
  1. Scan liver with USS and choose appropriate entry site
  2. Go through the liver to minimize the occurrence of a bile leak
  3. Anesthetise skin
  4. Place 22-gauge need into GB under US guidance
  5. Place catheter in GB in Tandem.
  6. Visualize catheter tip by the US before deploying catheter
  7. Aspirate bile for culture.
  8. Connect the catheter to the collecting bag
45
Q

WHat is this??

A

Bouveret syndrome is a gastric outlet obstruction produced by a gallstone impacted in the distal stomach or proximal duodenum. It was described by Leon Bouveret in 1896 (,1) and occurs most commonly in elderly women with a mean age of 68.6 years (,2).

46
Q

ERCP/MRCP finding:

irregular biliary duct with abrupt luminal narrowing

RFs: 4

A

cholangiocarcinoma

Risk factors:

PSC

UC

Liver parasites

choledochal cysts

47
Q

Pit falls of MRCP

A
  • Pseudofilling defects
  • pseudodilatations
  • nonvisualisation of the ducts
  • Filling defects are usually due to stones (dependant)
    • air (non-dependant_
    • tumours hemorrhage (dependant) or
    • sludge (dependant)
  • Infrequent causes of filing defects include
    • susceptibility artifact from adjacent clips,
    • metallic bile duct stents,
    • folds, or
    • flow voids (central
48
Q

Name variants of Cystic Duct Insertion

A
  • Normal
  • low union
  • parallel course
  • anterior spiral course
  • posterior spiral course
49
Q

what is this?

A

Peribiliary Cysts

  • Peribiliary cysts occur in the setting of chronic liver disease where it is a rare, benign, and often asymptomatic disorder. They consist of cystic formations around the intrahepatic biliary ducts, primarily in a hilar distribution. Unlike choledochal cysts (for example in Caroli disease), peribiliary cysts do not communicate with the biliary tree.
  • Related to the peribiliary glands.

Differential diagnosis

Imaging differential considerations include:

  • von Meyenburg complexes: although in this setting biliary hamartomas are more diffuse throughout the liver rather than hilar in distribution and would be more space out
  • Caroli disease: a congenital disorder involving multifocal intrahepatic choledochal cysts of the segmental intrahepatic bile ducts
50
Q

What are the indications for cholecystostomy?

A
  • Unexplained fever
  • suspected cholecytitis
    • rationale for catheter placement is to decompress an inflamed GB.
  • GB must be distended
51
Q

what is this?

What is the clinical triad

What types/forms of this are there?

A
  • Choledochal cysts
    • cystic dilatation of the CBD
      • type I fusiform
      • Type II saccular/diverticulum
    • lined with duodenal mucosa
    • Tupically occur in children and young adults
    • most common in Japan/asia
    • 20 fold increased risk of bile duct malignancy they are usually excised.
  • Clinical triad
    • jaundice
    • abdopain (infection of bile)
    • Palapble mass.
52
Q

What is the indication for percutaneous Biliary drainage?

What are the steps?

A
  • Indication: Biliary obstruction
  • steps after transhepatic cholangiogram:
    1. after cannulation of the bile duct, advance a nitinol guidewire (or the guide wire that comes with the one-stick access set) through the needle into the biliary system.
    2. Obtain as much purchase as possible.
    3. Remove needle
    4. Pass plastic catheter over guidewire.
    5. exchange guide wire for a 0.038 metal wire or Terumo, pass guidewire indo duodenum
    6. Dilate skin tract up to 12 Fr
    7. Place drainge catheter over guide wire (Cope, Ring catheters)
    8. Perform catheter injection with contrast material to adjust placement of side holes.
53
Q

what is this

A

Cholesterolosis Strawberry GB

  • Triglucerides and cholesterol are deponsitied in macrophages of the GB wall.
  • The cholesterol nodues stud the wall and give the GB the appearance of a strawberry
  • lipd deposits are echogenic and <1mm
  • no shadowing
  • inflammation is not a prominent feature
  • a/w multiple 0.5-1mm polyps
  • https://www.ultrasoundcases.info/unusual-cases-3748/
54
Q

Definition of Sludge

A
  • Sludge is echogenic bile
  • layering of particulate material within bile
    • calcium bilirubinate
    • cholesteral crystals
  • no posterior shaddowing
  • Causes
    • fasting (bc of decreased cholecystokinin CCK)
      • 10 days 30% of pts have sludge
      • 6 weeks 100% of pts
    • Hyper alimentation (decreased CCK)
    • Infection
    • obstruction
    • Stasis of GB

Cholecystokinin (CCK or CCK-PZ; from Greek chole, “bile”; cysto, “sac”; kinin, “move”; hence, move the bile-sac (gallbladder)) is a peptide hormone of the gastrointestinal system responsible for stimulating the digestion of fat and protein. Cholecystokinin, officially called pancreozymin, is synthesized and secreted by enteroendocrine cells in the duodenum, the first segment of the small intestine. Its presence causes the release of digestive enzymes and bile from the pancreas and gallbladder, respectively, and also acts as a hunger suppressant.[5][6]

55
Q

What is ERCP?

what are the complications 3

A
  • Contrast agent injection is performed thought the endoscope after cannulation of papilla of CBD
  • Complications
    • pancreatitis 5%
    • duodenal perforation
    • GI bleed
56
Q

What is papillary stenosis

how is it treated?

what are the 4 causes?

A
  • Sphincter of Oddi spasm
  • Treated with papillotomy
  • Causes
    • cholecystectomy
    • stones
    • trauma
    • AIDS cholangiopathy
57
Q

What are the indications for Transhepatic Cholangiogram?

A
  • Demonstration of biliary anatomy.
  • the first step before biliary drainage or stent placement.
  • PROCEDURE
    • RIGHT HEPATIC LOBE
      • Antibiotic coverage is routine
      • use a lateral midaxillary approach, advance one-stick system into the liver
      • attach extension tubing and syringe filled with contrast
      • slowly inject contrast while retracting the needly under fluoroscopy
      • repeat until opacification of bile ducts
    • LEFT HEPATIC LOBE
      • Antibiotic coverage is routine
      • use a midline approach, advance one stick system into a biliary radical under US guidance.
      • attach extension tubing and syringe filled with contrast
      • slowly inject contrast during fluoroscopy to confirm the biliary placement of the needle
      • Ensure the syringe is air-free in order to not obscure the view for future attempts.
58
Q

what is this?

A

The concentration of intravesicular calcium salts in longstanding cystic duct obstruction.

Radiographically, GB contents appear dense

59
Q

What sign is this and what are the other

Imaging features of Caroli disease?

A
  • Multiple cystic structures converging toward porta hepatis
  • beaded appearance of intrahepatic bile ducts
  • most of the cysts arranged in a branching pattern
  • central dot sign
    • very specific sign of Caroli disease in which portal radicals are partially or completely surrounded by abnormally dilated and ectatic bile ducts on both sonography and CT
  • Sludge, calculi in dilated ducts
60
Q

ERCP/MRCP finding:

round filling defects

A
  • Biliary stones
61
Q

Name the 3 complications of Sclerosisng cholangitis

A
  1. Cholangio ca 10%
  2. Biliary cirrhosis
  3. Portal hypertension
62
Q

Name the types of gall stones

A
  1. cholesterol stones are caused by preciptiation of supersaturated bile (western pop)
  2. pigment stones are the precipitate of calcium bilirubinate (asian pop)
  3. Mixed stones are the most common.
63
Q

associations of caroli disease

2

A
  • Medullary sponge kidney 80%
  • Infantile polycystic kidney disease
64
Q

What is the definition of Hyperplastic cholecystoses?

A
  • benign group of disease
  • accumulation of cholesterol and fats in the GB
  • Two forms
    • adenomyomatosis
    • cholesterolosis
  • no neoplastic potential
  • uncertain clinical significance
  • Commonly seen in cholecystectomy specimen
  • less commonly identified by US or cholecystogram

Gallbladder cholecystoses are conditions characterised by the accumulation of cholesterol (and other fats) in the gallbladder. There are two main forms:

adenomyomatosis: mucosal hyperplasia with growth toward the muscular layer - thickened muscular layer. Cholesterol accumulation is intraluminal (within the Rokitansky-Aschoff sinuses), therefore, lined by mucosal epithelium 2,3
cholesterolosis: mucosal hyperplasia with the accumulation of cholesterol esters and triglycerides in the macrophages of the lamina propria - appearance is known as “strawberry gallbladder” 2,3

65
Q

What are the disadvantages of MRCP over ERCP?

A
  • decreased spatial res, making MRCP less sensitive to abnormalites of the peripheral intrahepatic ducts (eg Sclerosing cholangitis) and pancreatic ductal side branches (chronic pancreatitis)
  • imaging in the physiologic, nondistened state which decreased the sensitive to detect subtle ductal anomalies
  • Cant perform therapeutic endoscopic or percut intervention for obstructing bile duct lesions.
  • therefore in pts with high clinical suspicion of CBD obstruction, ERCP should be the initial imaging modality to provide timely intervention
    • eg sphincterotomy
    • dilation
    • stent placement
    • stone removal
66
Q

Risk factors for Gall stones

6

A
  • Obesity
  • hemolytic anemia (pigment stones)
  • Abnormal enterohepatic circulation of bile salts (CD, SB resection)
  • Diabetes
  • Cirrhosis
  • Hyperparathyroidism
67
Q

Gall Bladder variants

A
  • Phrygian cap
  • junctional fold
    • fold between infundibulum and body. May be hyperechoic and cause posterior shaddowing
  • Agenesis of the GB Rare
  • more common causes of nonvisualised GB
    • previous cholecystectomy
    • non fasting
    • chronic cholecystitis
68
Q
A
69
Q

Causes of Biliary Enteric Fistulas

A
  • Chronic cholecystitis with erosion of a gall stone into the GIT 90%
  • Penetration of a posterior duodenal ulcer into the CHD 5%
  • Tumour
  • Trauma
70
Q

% of AIDS patients with Biliary abnormalities

A
  • 20%
    • GB wall thickening
    • cholelithiasis
    • Sludge
    • Biliary dilatation
    • Lymphadenopathy
    • Asctits
  • GB wall thickening is relatively common and may be marked. Cause unknown. Only symptomatic patients should be treated for acalculous cholecystitis which may be due to Cryptosporidium +/- CMV
71
Q

Name variations in Hepatic duct anatomy

A
  • normal in 60%
  • Right posterior ducts drain directly into LHD 20%
  • RIght posterior duct right anterior duct and LHD form the CHD 10%
72
Q

What is a cholecystostomy and who is it performed in?

A
  • Percutaneous cholecystostomy is often performed for acalculous cholecystitis in ICU patients with unexplained sepsis.
  • In these patients USS findings are not helpful in making the dx of acute cholecystitis and a trial of cholecystostomy is often warranted
  • clinical response is typically seen in 60% of pts
73
Q

Risk factors for Acalculus Cholecystitis

A
  • Trauma
  • Burns
  • Prolonged fasting
  • hyperalimentation
  • diabetes
  • AIDS
  • COlitis
  • hepatic arterial chemo
  • post partum
  • vascular insufficiency

overview

Acalculous cholecystitis is defined as cholecystitis that occurs without a gallstone.

This typically occurs in critically ill patients due to a combination of factors (e.g. bile stasis and hypoperfusion).

Acalculous cholecystitis often goes unrecognized initially, because of intubation and sedation. This can lead to a high rate of progression to gallbladder necrosis (50%) and perforation (10%).

The term “necrotizing cholecystitis” has been proposed for this disease, to emphasize its potentially malignant course.

pathogenesis

Pathogenesis may be summarized roughly as follows. In some ways, this may be conceptualized as a paralytic ileus of the gallbladder.

(1) Lack of enteral nutrition and hypoperfusion create a hypotonic, dilated gallbladder.

Distension of the gallbladder increases wall tension, further impairing perfusion of the gallbladder wall.

Biliary stasis causes concentration of biliary detergents, which may damage the gallbladder wall.

(2) Further complications ensue:

Necrosis and perforation of the gallbladder may occur.

Superinfection with enteric bacteria may occur (empyema of the gallbladder). Note that many cases of acalculous cholecystitis occur without bacterial infection.

https://emcrit.org/ibcc/acalculous-cholecystitis/

74
Q

USS features of Chronic Cholecystitis

A
  • GB wall thickening
    • fibrosis
    • chronic inflammation
  • Rokitansky-Aschoff sinuses (intramural epithelial crypts)
  • Gallstones
  • Failure of GB to contract in response to CCK
  • Porcelain GB:
    • wall calcifications
    • increased risk of GB carcinoma
  • Thickened gallbladder wall. Streaky echogenic lines from the anterior GB wall in keeping with comet-tail artifact. No gallstones.

Case Discussion

The comet-tail artifact is a type of ultrasound reverberation artifact caused by cholesterol crystals being trapped within Rokitansky-Aschoff sinuses in gallbladder adenomyomatosis.

75
Q

What are the indications and steps of Biliary Stent Placement?

A
  • Biliary stent placement
  • Indication:
    • malignant biliary stricture
    • inability to place an endoscopic stent
  • Steps post catheterization and decompression
    1. Inject existing catheter to determine exact site of stricture
    2. choose appropriate stent lengths
      • 42mm, 64mm, 94mm
    3. place ultra-stiff guide wire
    4. remove indwelling catheter
    5. place 8 Fr peel away sheath
    6. Deploy expandable stent (eg wall stent, 10mm diameter)
    7. Inject to confirm the location
    8. leave safety catheter in.
    9. Remove guidewire.
76
Q

What is this??

A
    • acute cholangitis
  • Infection of obstructed bile ducts
  • Ecoli > klebsiella > pseudomonas
  • Causes
    • choledocholithiasis
    • stricture
    • Sclerosing cholangitis
    • Infected drainage Catheter
    • Ampullary Carcinoma
  • Imaging features
    • Dialtation of intrahepatic ducts
      • dialted CBD
    • pigment stones and sludge in intrahepatic bile ducts
      • pathognomonic
    • Segmental hepatic atrophy
    • Liver abscess, pancreatitis

Figure 2 BAC in a patient with CBD stones. Coronal image from contrast material–enhanced multidetector computed tomography (CT) shows pus (arrowhead) layering within one of several dilated intrahepatic ducts (arrows). Intra-ductal sludge could have the same appearance. The patient underwent biliary drainage; abundant pus was aspirated.

https://pubs.rsna.org/doi/10.1148/rg.297095051