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Bililary ultrasound DR/ AMR SALAH 1 Dr /Amr Salah

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1 bililary ultrasound DR/ AMR SALAH 1 Dr /Amr Salah dramrsalah84@gmail.com

2 Contents 1- AnatomyNormal - Variant 2- CongenitalCholedochal cyst – caroli’s disease – biliary atresia 3- InfectiousAcute cholangitis – recurrent pyogenic cholangitis 4- IdiopathicPSC 5- StonesCholedocholithiasis – mirrizi’s syndrome 6- Benign neoplasmBiliary cystadenoma – bile duct adenoma- Biliary papillomatosis 7- Malignant neoplasmCholangiocarcinoma - Ampullary carcinoma – biliary cystadenocarcinoma 8- Trauma and postop Bile leak – Biloma – stent

3 Contents 3 Dr /Amr Salah dramrsalah84@gmail.com Anatomy and Anomalies- AtresiaBile duct wall thickeningContents : stone / mass / echogenicityDilatation : inside / outside / others Extra : estimation of jaundice Following : operation and stent

4 anatomy PART I Dr /Amr Salah dramrsalah84@gmail.com 4

5 5

6 Intra segmental Dr /Amr Salah dramrsalah84@gmail.com 6

7 7

8 8

9 9

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11 Dr /Amr Salah dramrsalah84@gmail.com 11

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13 Dr /Amr Salah dramrsalah84@gmail.com 13

14 Dr /Amr Salah dramrsalah84@gmail.com 14

15 Dr /Amr Salah dramrsalah84@gmail.com 15

16 Dr /Amr Salah dramrsalah84@gmail.com 16

17 Proximal >>>liver Distal >>>>pancreas and duodenum Order = division CHD >>>1 st order ( RT and LT)>>>>2 nd order Central >>>porta hepatis Peripheral >>>higher order Intra hepatic duct may be anterior or posterior or around the portal vein Dr /Amr Salah dramrsalah84@gmail.com 17

18 CHD :1 st – RT and LT 2 nd Dr /Amr Salah dramrsalah84@gmail.com 18

19 Dr /Amr Salah dramrsalah84@gmail.com 19

20 Visualization of 3 rd or higher order branches ?? Abnormal 2 nd to advanced higher less than 2 mm Dr /Amr Salah dramrsalah84@gmail.com 20

21 Dr /Amr Salah dramrsalah84@gmail.com 21

22 Dr /Amr Salah dramrsalah84@gmail.com 22 RP RA L 2

23 Normal The normal caliber of the CH/CBD max ~7mm May be 10 mm in older age and post surgical The site of insertion of the cystic duct to CHD>>>>CBD The common bile duct should measure less than 1 mm in neonates less than 2 mm in infants up to 1 year old less than 4 mm in older children and less than 7 mm in adolescents and adults. Dr /Amr Salah dramrsalah84@gmail.com 23

24 Biliary atresia Dr /Amr Salah dramrsalah84@gmail.com 24

25 Biliary atresia Congenital biliary disorder, which is characterized by an absence or severe deficiency of the extrahepatic biliary treebiliary tree It is one of the most common causes of neonatal cholestasis, causing cirrhosis immediately and leading to death and accounts for over half of children who undergo liver transplantation. cirrhosis Dr /Amr Salah dramrsalah84@gmail.com 25

26 Clinical presentation It precipitates within the first three months of life. Infants with biliary atresia may appear normal and healthy at birth. Most often, symptoms develop between two weeks to two months of life, and may include : jaundice (conjugated hyperbilirubinemia) jaundice dark yellow or brown urine pale or clay-colored (acholic) stools hepatomegaly Dr /Amr Salah dramrsalah84@gmail.com 26

27 Dr /Amr Salah dramrsalah84@gmail.com 27

28 Types There are two different forms of biliary atresia non-syndromic BA (~90%): isolated atresia of bile ducts syndromic BA (~10%): associated with various congenital anomalies such as polysplenia, asplenia, heterotaxy syndrome and intestinal malrotation.polyspleniaheterotaxy syndrome Dr /Amr Salah dramrsalah84@gmail.com 28

29 Ultrasound 1.Triangular cord sign triangular or tubular echogenic cord of fibrous tissue seen in the porta hepatis porta hepatis more than 4 mm thickness of the echogenic anterior wall of the right portal vein (EARPV) measured on a longitudinal ultrasound scan 2. larger hepatic arterial caliber an enlarged hepatic artery and hepatic arterial flow that extended to the hepatic surface were seen in all patients with BA 3. gallbladder ghost trial : atretic gall bladder + irregular contour + lack of complete mucosal lining Dr /Amr Salah dramrsalah84@gmail.com 29

30 Dr /Amr Salah dramrsalah84@gmail.com 30

31 Dr /Amr Salah dramrsalah84@gmail.com 31

32 Triangular cord sign Dr /Amr Salah dramrsalah84@gmail.com 32

33 TC sign Dr /Amr Salah dramrsalah84@gmail.com 33

34 Gall bladder ghost sign Dr /Amr Salah dramrsalah84@gmail.com 34

35 Prominent subcapsular HA Dr /Amr Salah dramrsalah84@gmail.com 35

36 Biliary Atresia Dr /Amr Salah dramrsalah84@gmail.com 36 Ghost GB Enlarged HA Pv TC sign HA capsular sign

37 Non biliary atresia Dr /Amr Salah dramrsalah84@gmail.com 37 No TC sign Normal GB Normal diameter HA PV NO HA capsular sign

38 Contents 1- AnatomyNormal - Variant 2- CongenitalCholedochal cyst – caroli’s disease – biliary atresia 3- InfectiousAcute cholangitis – recurrent pyogenic cholangitis – 4- IdiopathicPSC 5- StonesCholedocholithiasis – mirrizi’s syndrome 6- Benign neoplasmBiliary cystadenoma – bile duct adenoma- Biliary papillomatosis 7- Malignant neoplasmCholangiocarcinoma - Ampullary carcinoma – biliary cystadenocarcinoma 8- Trauma and postop Bile leak – biloma – benign stricture

39 Contents 39 Dr /Amr Salah dramrsalah84@gmail.com Anatomy and Anomalies/AtresiaBile duct wall thickeningContents : stone / mass / echogenicityDilatation : inside – outside - others Extra : estimation of jaundice Following : operation and stent

40 Dr /Amr Salah dramrsalah84@gmail.com 40

41 Bile duct wall thickening PART II Dr /Amr Salah dramrsalah84@gmail.com 41

42 Causes 1.Cholangitis : ascending – recurrent pyogenic – primary sclerosing 2.Cholangiocarcinoma 3.HCC 4.AIDS cholangiopathy 5.IBD Dr /Amr Salah dramrsalah84@gmail.com 42

43 Causes of CBD wall thickening Normal diameter ~ 1.5 mm More than 5 mm Cholangicarcinoma focalDiffuse Concentric Especially in the distal CBD Pancreatitis Pancreatic cancer CBD stone Acute / ascending cholangitis Recurrent pyogenic cholangitis Eccentric Cholangiocarcinoma PSC Cholangiohepatopathy PSC Dr /Amr Salah dramrsalah84@gmail.com 43

44 Dr /Amr Salah dramrsalah84@gmail.com 44

45 Cholangitis Broad descriptive term / Inflammation of the bile duct It has many forms and can arise from a number of situations: primary sclerosing cholangitis infective cholangitis Acute/ascending cholangitis Recurrent pyogenic cholangitis - oriental cholangitis chemotherapy induced cholangitis eosinophilic cholangitis Dr /Amr Salah dramrsalah84@gmail.com 45

46 Primary sclerosing cholangitis Dr /Amr Salah dramrsalah84@gmail.com 46

47 Primary sclerosing cholangitis Primary sclerosing >>>>secondary sclerosing cholangitis Primary = unknown cause Causes of secondary : AIDS – cancer – radiation – post operative Dr /Amr Salah dramrsalah84@gmail.com 47 1ry Sclerosing >>>>>1ry biliary cholangitis / cirrhosis Biliary cirrhosis >>>>affect mainly the distal biliary radicels …just you see cirrhosis by imaging Women > men High antibody titers ( AMA)

48 Dr /Amr Salah dramrsalah84@gmail.com 48

49 Primary sclerosing cholangitis An uncommon idiopathic inflammatory condition, which affects the biliary tree resulting in multiple strictures and eventual cirrhosisstricturescirrhosis The diagnosis can be made when there are classical imaging features in the correct clinical context, and secondary causes of cholangitis have been excluded PSC is strongly associated with inflammatory bowel disease (IBD) (in 70% cases ), especially ulcerative colitis and thus shares similar demographics: young to middle-aged males (≈4 th decade) are most frequently affectedinflammatory bowel disease (IBD)ulcerative colitis Dr /Amr Salah dramrsalah84@gmail.com 49

50 Best diagnostic clue Beaded appearance Location : CBD : almost always affected Intra and extra HBR : 70 – 90 % intra or extra alone : less than 20 % Dr /Amr Salah dramrsalah84@gmail.com 50

51 Clinical presentation Middle age male : rule of 70% 70 % male – 70 % ulcerative colitis – 70 % less than 45y Asymptomatic individuals are identified upon investigation of persistently deranged liver function tests fatigue. More specific symptoms include pruritus, jaundice or GI bleeding Elevated serum alkaline phosphatase Dr /Amr Salah dramrsalah84@gmail.com 51

52 Associations ulcerative colitis Sjogren syndrome retroperitoneal fibrosis mediastinal fibrosis Riedel thyroiditis orbital pseudotumor antibody titers are usually absent or low. Liver function tests will usually have a cholestatic pattern with elevated alkaline phosphatase (ALP) and bilirubin Dr /Amr Salah dramrsalah84@gmail.com 52

53 Ultrasound Bright echogenic portal triad Signs of portal hypertension Irregular wall thickening ( beaded) Proximal biliary dilatation Gall bladder abnormalities : stones / thick wall …50% DD : bilharziasis Dr /Amr Salah dramrsalah84@gmail.com 53

54 Dr /Amr Salah dramrsalah84@gmail.com 54

55 Dr /Amr Salah dramrsalah84@gmail.com 55

56 CBD Dr /Amr Salah dramrsalah84@gmail.com 56

57 Dr /Amr Salah dramrsalah84@gmail.com 57

58 Radiological findings The entire biliary tree (both intra and extrahepatic) may be involved, with multiple strictures scattered along its length The end result of PSC is cirrhosis which is usually characterized by a markedly distorted biliary tract with atrophy of the entire liver with the exception of the caudate lobe which is hypertrophied in almost all cases (68-98%)cirrhosiscaudate lobe Atrophy involving the left lobe is a feature which somewhat distinguishes it from cirrhosis from other causes, in which the left lobe is usually hypertrophied Dr /Amr Salah dramrsalah84@gmail.com 58

59 Complications cholangiocarcinoma develops in ~15% patients cholangiocarcinoma colorectal cancer 4x greater risk compared to IBD patients without PSC 10x greater risk compared to general population hepatocellular carcinoma: appears to be not increased beyond other causes of cirrhosis hepatocellular carcinoma Dr /Amr Salah dramrsalah84@gmail.com 59

60 Differential diagnosis Cirrhosis Caudate lobe not as frequently or as markedly enlarged left lobe usually also hypertrophied secondary sclerosing cholangitis AIDS associated cholangitis biliary strictures from other causes, e.g. surgery, ischaemia primary biliary cirrhosis young women more frequently affected high antibody titres Dr /Amr Salah dramrsalah84@gmail.com 60

61 PSC P : pruritus– beaded – portal HTN – proximal dilatation– DD: bilharziasis S : Seventy rule 70 % middle age – 70 % male – 70 % UC C : Eventually with cirrhosis Dr /Amr Salah dramrsalah84@gmail.com 61

62 Contents 1- AnatomyNormal - Variant 2- CongenitalCholedochal cyst – caroli’s disease – biliary atresia 3- InfectiousAcute cholangitis – recurrent pyogenic cholangitis 4- IdiopathicPSC 5- StonesCholedocholithiasis – mirrizi’s syndrome 6- Benign neoplasmBiliary cystadenoma – bile duct adenoma- Biliary papillomatosis 7- Malignant neoplasmCholangiocarcinoma - Ampullary carcinoma – biliary cystadenocarcinoma 8- Trauma and postop Bile leak – biloma – benign stricture

63 ascending cholangitis Dr /Amr Salah dramrsalah84@gmail.com 63

64 Ascending cholangitis / acute cholangitis form of cholangitis and refers to the acute bacterial infection of the biliary tree.cholangitisbiliary tree It is a condition with high mortality that necessitates emergent biliary decompression. The classical presentation is the Charcot triad of fever, right upper quadrant abdominal pain, and jaundice, which is only seen in ~40% of patients.Charcot triad Patients can also present with Reynold pentad, which is Charcot triad with shock and altered mental statusReynold pentad Dr /Amr Salah dramrsalah84@gmail.com 64

65 Etiology Gram-negative enteric bacteria, most commonly Escherichia coli, are the primary pathogens. Acute cholangitis is seen in the setting of biliary tree obstruction : choledocholithiasis (~80%) choledocholithiasis malignancy (~20%) sclerosing cholangitis biliary tree procedures, e.g. ERCPERCP Dr /Amr Salah dramrsalah84@gmail.com 65

66 Radiographic features Acute cholangitis is typically a clinical diagnosis with imaging performed to determine if there is evidence of : 1.intrahepatic and/or extrahepatic duct dilatation (indicating obstruction/stasis) 2.bile duct wall thickening or focal outpouchings 3.cholelithiasis/choledocholithiasischolelithiasischoledocholithiasis Dr /Amr Salah dramrsalah84@gmail.com 66

67 Ultrasound A hallmark finding is thickening of the walls of the bile ducts in the appropriate clinical setting. Ultrasound may also show biliary dilatation with calculi, with or without pus, which appears as debris material within the common bile duct. Periportal hypo/hyper echogenicity adjacent to dilated IHBR Gall bladder : thick wall ± stone Liver : intrahepatic abscess Dr /Amr Salah dramrsalah84@gmail.com 67

68 Dr /Amr Salah dramrsalah84@gmail.com 68 PvCBD

69 Dr /Amr Salah dramrsalah84@gmail.com 69

70 Dr /Amr Salah dramrsalah84@gmail.com 70

71 Dr /Amr Salah dramrsalah84@gmail.com 71

72 Pathognomonic / periportal hyperechogenicty Dr /Amr Salah dramrsalah84@gmail.com 72

73 Dr /Amr Salah dramrsalah84@gmail.com 73

74 To recap PSC P : pruritus – beaded – bilharziasis S : seventy 70% rule C : cirrhosis Dr /Amr Salah dramrsalah84@gmail.com 74 Acute /Ascending cholangitis A : ascending pattern C : clinical

75 Recurrent pyogenic cholangitis Dr /Amr Salah dramrsalah84@gmail.com 75

76 Recurrent pyogenic / oriental cholangitis Dr /Amr Salah dramrsalah84@gmail.com 76

77 Recurrent pyogenic / oriental cholangitis intra and extrahepatic bile duct strictures and dilatation with an intraductal pigmented stone formation. Clinical presentation Residing in or immigrated from Southeast Asia The common clinical presentation is that of recurrent right upper quadrant pain, fever, and jaundice.jaundice Leukocytosis with elevated alkaline phosphatase and bilirubin are seen. Dr /Amr Salah dramrsalah84@gmail.com 77

78 Best diagnostic clue 1.Intra and extra hepatic biliary stones within dilated duct 2.No gall bladder stones May the stones fills the duct give serpiginous pattern Dr /Amr Salah dramrsalah84@gmail.com 78

79 Dr /Amr Salah dramrsalah84@gmail.com 79

80 Dr /Amr Salah dramrsalah84@gmail.com 80

81 Dr /Amr Salah dramrsalah84@gmail.com 81

82 Dr /Amr Salah dramrsalah84@gmail.com 82

83 Dr /Amr Salah dramrsalah84@gmail.com 83

84 To recap Recurrent pyogenic cholangitis R : radicles dilatation / liver P : presence of pigmented stones C : coming from southeast Asia Dr /Amr Salah dramrsalah84@gmail.com 84 PSC P : pruritus – beaded – bilharziasis S : seventy 70% rule C : cirrhosis acute /Ascending cholangitis A : ascending pattern C : clinical

85 Contents 1- AnatomyNormal - Variant 2- CongenitalCholedochal cyst – caroli’s disease – biliary atresia 3- InfectiousAcute cholangitis – recurrent pyogenic cholangitis 4- IdiopathicPSC 5- StonesCholedocholithiasis – mirrizi’s syndrome 6- Benign neoplasmBiliary cystadenoma – bile duct adenoma- Biliary papillomatosis 7- Malignant neoplasmCholangiocarcinoma - Ampullary carcinoma – biliary cystadenocarcinoma 8- Trauma and postop Bile leak – biloma – benign stricture

86 Contents 86 Dr /Amr Salah dramrsalah84@gmail.com Anatomy and anomaliesBile duct wall thickeningContents : stone / mass / echogenicityDilatation : inside – outside - others Extra : estimation of jaundice Following : operation and stent

87 Abnormal intra ductal Contents PART III Dr /Amr Salah dramrsalah84@gmail.com 87

88 DD 1.Stone 2.Mass 3.Air Blood Parasite Sludge ball Pus Dr /Amr Salah dramrsalah84@gmail.com 88

89 Intraductal stones Dr /Amr Salah dramrsalah84@gmail.com 89

90 Bile duct stones / Choledocholithiasis Clinical presentation Stones within the bile ducts are often asymptomatic and may be found incidentally, however, more frequently they lead to symptomatic presentation with: 1.biliary colicbiliary colic 2.ascending cholangitisascending cholangitis 3.obstructive jaundiceobstructive jaundice 4.acute pancreatitisacute pancreatitis Dr /Amr Salah dramrsalah84@gmail.com 90

91 Primary and secondary Dr /Amr Salah dramrsalah84@gmail.com 91

92 Primary vs. secondary Secondary 95% : stone migrated from gall bladder 1ry 5% : de nevo formation within the biliary tree Causes : P : Post operative /trauma - Parasite C : Congenital – Cholangitis – Chronic hemolytic anemia Dr /Amr Salah dramrsalah84@gmail.com 92

93 Dr /Amr Salah dramrsalah84@gmail.com 93

94 Dr /Amr Salah dramrsalah84@gmail.com 94

95 Dr /Amr Salah dramrsalah84@gmail.com 95

96 crescent sign: bile eccentrically outlines luminal stone, creating a low attenuation crescent Dr /Amr Salah dramrsalah84@gmail.com 96

97 Dr /Amr Salah dramrsalah84@gmail.com 97

98 Dr /Amr Salah dramrsalah84@gmail.com 98

99 Contents 1- AnatomyNormal - Variant 2- CongenitalCholedochal cyst – caroli’s disease – biliary atresia 3- InfectiousAcute cholangitis – recurrent pyogenic cholangitis 4- IdiopathicPSC 5- StonesCholedocholithiasis – mirrizi’s syndrome 6- Benign neoplasmBiliary cystadenoma – bile duct adenoma- Biliary papillomatosis 7- Malignant neoplasmCholangiocarcinoma - Ampullary carcinoma – biliary cystadenocarcinoma 8- Trauma and postop Bile leak – biloma – benign stricture

100 Intraductal masses Dr /Amr Salah dramrsalah84@gmail.com 100

101 Intra ductal mass Dr /Amr Salah dramrsalah84@gmail.com 101

102 Cholangiocarcinoma Infiltrative mass + biliary dilatation 90% extra hepatic 10 % intra hepatic 50 % distal CBD Check signs of malignancy Dr /Amr Salah dramrsalah84@gmail.com 102

103 Dr /Amr Salah dramrsalah84@gmail.com 103

104 Dr /Amr Salah dramrsalah84@gmail.com 104 lesion CBD

105 Distal cholangiocarcinoma Dr /Amr Salah dramrsalah84@gmail.com 105

106 Dr /Amr Salah dramrsalah84@gmail.com 106 Distal cholangiocarcinoma

107 Dr /Amr Salah dramrsalah84@gmail.com 107 CBD

108 Intraductal air Dr /Amr Salah dramrsalah84@gmail.com 108

109 Pneumobilia, also known as aerobilia Recent biliary instrumentation : ERCP, PTC Incompetent sphincter of Oddi sphincterotomy (~50% pneumobilia at 1 year) following passage of a gallstone Congenital biliary-enteric surgical anastomosis : Cholecystoenterostomy Whipple procedure spontaneous biliary-enteric fistula gallstone ileus peptic ulcer disease traumatic neoplasm, eg. cholangiocarcinoma, ampullary cancer Dr /Amr Salah dramrsalah84@gmail.com 109

110 Radiographic features Pneumobilia is typically seen as linear branching gas within the liver most prominent in central large caliber ducts as the flow of bile pushes gas toward the hilum. This is in contrast to portal venous gas where peripheral small caliber branching gas is usually seen due to the hepatopetal flow of blood away from the hilum.portal venous gashepatopetal flow portal venous gas: peripheral common bile duct gas: central Dr /Amr Salah dramrsalah84@gmail.com 110

111 Dr /Amr Salah dramrsalah84@gmail.com 111

112 Dr /Amr Salah dramrsalah84@gmail.com 112

113 Dr /Amr Salah dramrsalah84@gmail.com 113

114 Dr /Amr Salah dramrsalah84@gmail.com 114

115 Bright echogenic foci with linear configuration Dr /Amr Salah dramrsalah84@gmail.com 115

116 Intraductal air vs. intra ductal stone Dr /Amr Salah dramrsalah84@gmail.com 116

117 Dr /Amr Salah dramrsalah84@gmail.com 117

118 Dr /Amr Salah dramrsalah84@gmail.com 118

119 Dr /Amr Salah dramrsalah84@gmail.com 119

120 Dr /Amr Salah dramrsalah84@gmail.com 120

121 Dr /Amr Salah dramrsalah84@gmail.com 121

122 DD Portal vein gases : mostly peripheral Intra ductal stones : posterior shadowing Calcified granuloma : not related to portal tract Dr /Amr Salah dramrsalah84@gmail.com 122

123 Dr /Amr Salah dramrsalah84@gmail.com 123 Portal vein gases peripheral Common bile + biliary gases Central DD : P with P and C with C

124 DD 1.Stone 2.Mass 3.Air Blood Parasite Sludge ball Pus Dr /Amr Salah dramrsalah84@gmail.com 124

125 Haemobilia Etiology Iatrogenic: surgical or percutaneous procedures (~67%) Trauma (~5%) associated with pseudoaneurysm formation from central liver traumapseudoaneurysmliver trauma may manifest several (2-4) weeks after the initial injury Vascular malformations (7%) e.g. hepatic artery aneurysm or arteriovenous malformation can cause massive hemobilia Malignancy (e.g. hepatocellular carcinoma - most common, gallbladder metastases)hepatocellular carcinomagallbladder metastases Dr /Amr Salah dramrsalah84@gmail.com 125

126 Dr /Amr Salah dramrsalah84@gmail.com 126

127 Dr /Amr Salah dramrsalah84@gmail.com 127 CBD

128 Dr /Amr Salah dramrsalah84@gmail.com 128 CBD

129 Sludge Dr /Amr Salah dramrsalah84@gmail.com 129

130 Dr /Amr Salah dramrsalah84@gmail.com 130

131 Pus = clinical Dr /Amr Salah dramrsalah84@gmail.com 131 CBD

132 Clinical Dr /Amr Salah dramrsalah84@gmail.com 132

133 Biliary ascaris Dr /Amr Salah dramrsalah84@gmail.com 133

134 Dr /Amr Salah dramrsalah84@gmail.com 134

135 Biliary ascaris Dr /Amr Salah dramrsalah84@gmail.com 135

136 Dr /Amr Salah dramrsalah84@gmail.com 136

137 Dr /Amr Salah dramrsalah84@gmail.com 137

138 DD 1.Stone : hyper echoic with distal shadowing 2.Mass : iso echoic with ?? Internal vascularity 3.Air : hyper echoic with dirty shadow Blood : history of trauma / recent surgery Parasite : parallel lines / gall bladder ascaris Sludge ball : sludge in GB Pus : clinical Dr /Amr Salah dramrsalah84@gmail.com 138

139 Contents 139 Dr /Amr Salah dramrsalah84@gmail.com Anatomy and Anomalies/AtresiaBile duct wall thickeningContents : stone / mass / echogenicityDilatation : inside – outside - others Extra : estimation of jaundice Following : operation and stent

140 Dilatation of the biliary tree PART IV Dr /Amr Salah dramrsalah84@gmail.com 140

141 Dr /Amr Salah dramrsalah84@gmail.com 141

142 Dr /Amr Salah dramrsalah84@gmail.com 142

143 Dr /Amr Salah dramrsalah84@gmail.com 143

144 Dr /Amr Salah dramrsalah84@gmail.com 144

145 N.B: 1- What it the meaning of dilatation ?? intrahepatic bile ducts : >2 mm, >40% of adjacent portal vein ( double parallel/duct signs ) extrahepatic bile ducts : >6 mm +1 mm per decade above 60 years of age, >10 mm post-cholecystectomy 2 - Level of obstruction ?? Focal intra hepatic – diffuse intra hepatic – extra hepatic – intra and extra 3 - Cause of obstruction ?? Inside – outside – others Dr /Amr Salah dramrsalah84@gmail.com 145

146 Double parallel /duct sign Dr /Amr Salah dramrsalah84@gmail.com 146

147 Dr /Amr Salah dramrsalah84@gmail.com 147

148 Dr /Amr Salah dramrsalah84@gmail.com 148

149 Double duct sign Dr /Amr Salah dramrsalah84@gmail.com 149

150 Dr /Amr Salah dramrsalah84@gmail.com 150

151 Dr /Amr Salah dramrsalah84@gmail.com 151

152 Causes Inside: Stones – mass – air – pus – sludge – ascaris – blood Mimics : Mirrizi syndrome Outside : intra hepatic – hilar – extra hepatic Others: Congenital : cariole's disease – choledochal cyst Infection : acute cholangitis – recurrent pyogenic – PSC Tumor : ampullary cancer Other : Sphincter of oddi dyskinesia - Pregnancy Dr /Amr Salah dramrsalah84@gmail.com 152

153 Classification Dr /Amr Salah dramrsalah84@gmail.com 153 InsideOutsideOthers

154 Inside Dr /Amr Salah dramrsalah84@gmail.com 154

155 Inside : mimics Dr /Amr Salah dramrsalah84@gmail.com 155

156 Dr /Amr Salah dramrsalah84@gmail.com 156

157 Mimics : Mirizzi syndrome extrinsic compression of an extrahepatic biliary duct from one or more calculi within the cystic duct or gallbladdercystic ductgallbladder Patients may present with recurrent episodes of jaundice and cholangitis.jaundicecholangitis It can be associated with acute cholecystitis. acute cholecystitis Fistulae can develop between the gallbladder and the common duct, and the stone may pass into the common duct. Dr /Amr Salah dramrsalah84@gmail.com 157

158 Dr /Amr Salah dramrsalah84@gmail.com 158

159 Dr /Amr Salah dramrsalah84@gmail.com 159

160 Mirrizi syndrome Dr /Amr Salah dramrsalah84@gmail.com 160

161 Mirrizi syndrome Dr /Amr Salah dramrsalah84@gmail.com 161

162 Dr /Amr Salah dramrsalah84@gmail.com 162

163 Outside Level Intra hepatic ( lobar ) : cholangiocarcinoma - HCC Hilar ( bi lobar ): klatskin tumor – lymph nodes Pancreatic (extra hepatic) : pancreatic head mass – pancreatitis Dr /Amr Salah dramrsalah84@gmail.com 163

164 Bilobar vs. lobar Dr /Amr Salah dramrsalah84@gmail.com 164

165 Cholangiocarcinoma It tends to have a poor prognosis and high morbidity. It is the second most common primary hepatic tumour, with intrahepatic cholangiocarcinomas (ICCs) accounting for 10-20% of primary liver tumours.primary hepatic tumour Dr /Amr Salah dramrsalah84@gmail.com 165

166 Dr /Amr Salah dramrsalah84@gmail.com 166

167 Dr /Amr Salah dramrsalah84@gmail.com 167

168 Dr /Amr Salah dramrsalah84@gmail.com 168

169 Dr /Amr Salah dramrsalah84@gmail.com 169

170 Dr /Amr Salah dramrsalah84@gmail.com 170

171 Dr /Amr Salah dramrsalah84@gmail.com 171

172 Dr /Amr Salah dramrsalah84@gmail.com 172

173 Porta hepatis lymph nodes Dr /Amr Salah dramrsalah84@gmail.com 173

174 Dr /Amr Salah dramrsalah84@gmail.com 174

175 Dr /Amr Salah dramrsalah84@gmail.com 175

176 Pancreatic : benign vs. malignant Dr /Amr Salah dramrsalah84@gmail.com 176 Malignant compressionBenign compression

177 Normal pancreas Dr /Amr Salah dramrsalah84@gmail.com 177

178 Pancreatic head mass Dr /Amr Salah dramrsalah84@gmail.com 178

179 Dr /Amr Salah dramrsalah84@gmail.com 179

180 Pancreatic duct dilatation Dr /Amr Salah dramrsalah84@gmail.com 180

181 Pancreatitis Dr /Amr Salah dramrsalah84@gmail.com 181

182 Pancreatitis Dr /Amr Salah dramrsalah84@gmail.com 182

183 Dr /Amr Salah dramrsalah84@gmail.com 183

184 Pancreas Dr /Amr Salah dramrsalah84@gmail.com 184

185 Dilatation with no masses Congenital : cariole's disease – choledochal cyst Infection : acute cholangitis – recurrent pyogenic – PSC Tumor : ampullary cancer / cholangiocarcinoma Other : Sphincter of oddi dyskinesia - Pregnancy Dr /Amr Salah dramrsalah84@gmail.com 185

186 Choledochal cyst Dr /Amr Salah dramrsalah84@gmail.com 186

187 Choledochal cyst congenital cystic dilatations of the biliary treebiliary tree Although they may be discovered at any age, 60% are diagnosed before the age of 10 years There is a strong female predilection with M:F ratio of 1:4. Dr /Amr Salah dramrsalah84@gmail.com 187

188 Todani classification 0 >>>normal 1 >> most common ( extra) Two >>diverticulum Three > choledococele 4 > second most common ( extra /intra) 5>>>caroli’s disease (intra) Dr /Amr Salah dramrsalah84@gmail.com 188

189 Dr /Amr Salah dramrsalah84@gmail.com 189

190 Dr /Amr Salah dramrsalah84@gmail.com 190

191 Complications stone formation: most common malignancy cholangiocarcinoma lifetime incidence 10-15% the cyst may rupture leading to bile peritonitis most frequently seen in neonates pancreatitis Dr /Amr Salah dramrsalah84@gmail.com 191

192 Type1 Dr /Amr Salah dramrsalah84@gmail.com 192

193 Type 1 Dr /Amr Salah dramrsalah84@gmail.com 193

194 Dr /Amr Salah dramrsalah84@gmail.com 194

195 Complicated by cholangiocarcinoma Dr /Amr Salah dramrsalah84@gmail.com 195

196 Dr /Amr Salah dramrsalah84@gmail.com 196

197 Dr /Amr Salah dramrsalah84@gmail.com 197

198 Dr /Amr Salah dramrsalah84@gmail.com 198

199 Type IV : intra + extra Dr /Amr Salah dramrsalah84@gmail.com 199

200 Type 5 : Caroli disease congenital disorder comprising of multifocal cystic dilatation of segmental intrahepatic bile ducts Clinical presentation Presentation is in childhood or young adulthood. The simple type presents with RUQ pain and recurrent attacks of cholangitis with fever and jaundice.jaundice The periportal fibrosis ( syndrome) type may present with pain or signs of portal hypertension, including hematemesis from esophageal varices Dr /Amr Salah dramrsalah84@gmail.com 200

201 Associations simple Caroli disease is uncommon; it occurs more frequently with congenital hepatic fibrosis, constituting the Caroli syndromecongenital hepatic fibrosis medullary sponge kidney autosomal dominant polycystic kidney disease (ADPKD) autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease (ARPKD) autosomal recessive polycystic kidney disease Dr /Amr Salah dramrsalah84@gmail.com 201

202 Radiological features Ultrasound may show dilated intrahepatic bile ducts (IHBD) intraductal bridging: echogenic septa traversing the dilated bile duct lumen small portal venous branches partially or completely surrounded by dilated bile ducts intraductal calculi CT multiple hypodense rounded areas which are inseparable from the dilated intrahepatic bile ducts “central dot” sign enhancing dots within the dilated intrahepatic bile ducts, representing portal radicles 1 Dr /Amr Salah dramrsalah84@gmail.com 202

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207 Contents 1- AnatomyNormal - Variant 2- CongenitalCholedochal cyst – caroli’s disease – biliary atresia 3- InfectiousAcute cholangitis – recurrent pyogenic cholangitis 4- IdiopathicPSC 5- StonesCholedocholithiasis – mirrizi’s syndrome 6- Benign neoplasmBiliary cystadenoma – bile duct adenoma- Biliary papillomatosis 7- Malignant neoplasmCholangiocarcinoma - Ampullary carcinoma – biliary cystadenocarcinoma 8- Trauma and postop Bile leak – biloma – benign stricture

208 Contents 208 Dr /Amr Salah dramrsalah84@gmail.com Anatomy and Anomalies/AtresiaBile duct wall thickeningContents : stone / mass / echogenicityDilatation : inside – outside - others Extra : estimation of jaundice Following : operation and stent

209 Estimation of jaundice PART V Dr /Amr Salah dramrsalah84@gmail.com 209

210 Jaundice Dr /Amr Salah dramrsalah84@gmail.com 210

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212 Jaundice Jaundice refers to a clinical sign of hyperbilirubinaemia (serum bilirubin >2.5 mg/dL) which has many causes. It is often a clue to a diagnosis.hyperbilirubinaemia It can be largely divided into two types: non-obstructive, i.e. prehepatic and hepatic causes obstructive, i.e. posthepatic causes Imaging has a major role in detecting the obstructive causes. Dr /Amr Salah dramrsalah84@gmail.com 212

213 Causes prehepatic haemolytic anaemia / hypersplenism hepatic acute hepatitis / acute liver failure / cirrhosis /Gilbert syndrome post-hepatic (or obstructive jaundice) Benign causes Stone strictures, e.g. post-inflammatory/infectious, primary sclerosing cholangitis, traumatic or operativetraumatic or external biliary tree compression, e.g. pancreatic pseudocyst, Mirizzi syndrome Malignant causes portal lymphadenopathy / Cholangiocarcinoma /Carcinoma of head of pancreas / HCC Dr /Amr Salah dramrsalah84@gmail.com 213

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215 Jaundice in infant Unconjugated hyperbilirubinemia is a normal physiologic event that occurs in approximately 60% of normal full-term infants and in 80% of preterm infants. The bilirubin level normally increases by day 2–3 and peaks by day 5–7, reaching as high as 12 mg/dL in normal full-term babies and up to 14 mg/dL in normal premature infants by the end of the first week of life Dr /Amr Salah dramrsalah84@gmail.com 215

216 Risk 1.The onset of jaundice within the first 24 hours of life 2.Rate of rise of serum bilirubin levels greater than 5 mg/dL in 24 hours 3.Direct bilirubin level greater than 1 mg/dL at any time 4.The persistence or new onset of jaundice in infants 2 weeks of age or older may no longer be physiologic The three most common causes of jaundice in neonates are hepatitis, biliary atresia, and choledochal cyst Dr /Amr Salah dramrsalah84@gmail.com 216

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218 Post operative stent / Biloma PART VI Dr /Amr Salah dramrsalah84@gmail.com 218

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222 Complicated by pancreatitis Dr /Amr Salah dramrsalah84@gmail.com 222

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225 Biloma  80-year-old woman presented with a cystic liver lesion following a laparoscopic cholecystectomy.  Biloma.  Extra biliary collections of bile. they can be either intra- or extrahepatic. Dr /Amr Salah dramrsalah84@gmail.com 225

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227 A Anatomy Atresia Division – measurements – anomalies TC signs – ghost gall bladder – dilated HA Capsular HA sign B : bile duct wall thickening PSC AC RPC P : beaded-pruiritis / S:70 rule / C : cirrhosis A : acute / C : clinical R : radicles / P: pigmented stone / C:coming from asia C : contents Stone Air Mass Others: : shadow / echogenic / GB stones : shadowing / echogenic /moving : soft tissue / vascularity : pus / blood : clinical parasites/sludge ball D : dilatation Intra Extra Others : contents : level of obstruction : intra hepatic / central / distal CBD : choledochal cyst / pregnancy / infectious / sphincter of oddi E : estimation of jaundice Adult Neonates F following operation Stent Biloma : normal / complicated : history of trauma / surgery 227

228 THANK YOU Dr /Amr Salah dramrsalah84@gmail.com 228


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