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Ultrasound findings in portal
hypertension
Durr-e-Sabih
MBBS. MS. FRCP. FANMB
Director MINAR- Multan
PAKISTAN
dsabih@yahoo.com
Portal hypertension
o Normal portal vein pressure is 5-10mm Hg
(14 cm H20)
o Wedge pressure or direct portal vein
pressure >5mm Hg than IVC
o Portal vein pressure >30cm H20
Portal hypertension
Presinusoidal-extrahepatic
o Portal and/or splenic vein
thrombosis
Presinusoidal-intrahepatic
o Primary biliary cirrhosis
o Schistosomiasis
o Congenital Hepatic Fibrosis
o Idiopathic noncirrhotic fibrosis
o Wilson’s disease
o Myelofibrosis
o Toxins (Polyvinyl chloride,
Methotrexate, arsenic)
Sinusoidal
o Portal cirrhosis
o Sclerosing cholangitis
o Diffuse metastatic disease
Post sinusoidal
o Budd Chiari Syndrome
o CCF
o Constrictive pericarditis
Portal hypertension
Presinusoidal-extrahepatic
o Portal and/or splenic vein
thrombosis
Presinusoidal-intrahepatic
o Primary biliary cirrhosis
o Schistosomiasis
o Congenital Hepatic Fibrosis
o Idiopathic noncirrhotic fibrosis
o Wilson’s disease
o Myelofibrosis
o Toxins (Polyvinyl chloride,
Methotrexate, arsenic)
Sinusoidal
o Portal cirrhosis
o Sclerosing cholangitis
o Diffuse metastatic disease
Post sinusoidal
o Budd Chiari Syndrome
o CCF
o Constrictive pericarditis
Portal hypertension
Presinusoidal-extrahepatic
o Portal and/or splenic vein
thrombosis
Presinusoidal-intrahepatic
o Primary biliary cirrhosis
o Schistosomiasis
o Congenital Hepatic Fibrosis
o Idiopathic noncirrhotic fibrosis
o Wilson’s disease
o Myelofibrosis
o Toxins (Polyvinyl chloride,
Methotrexate, arsenic)
Sinusoidal
o Portal cirrhosis
o Sclerosing cholangitis
o Diffuse metastatic disease
Post sinusoidal
o Budd Chiari Syndrome
o CCF
o Constrictive pericarditis
Where do we stand?
o Ultrasound of the liver surface is a useful diagnostic tool
in patients at risk of CLD when assessing whether they
should undergo a liver biopsy. Meta Analysis, 29
studies.1
o Ultrasound is accurate …and may identify cirrhosis
even in the absence of a typical histopathological
pattern.2
o Low frequency ultrasonography is not a sensitive test for
the diagnosis of liver cirrhosis in daily clinical practice.3
1Allan R, Thoirs K, Phillips M. Accuracy of ultrasound to identify chronic liver disease. World J Gastroenterol. 2010 Jul
28;16(28):3510-20.
2Giani S, Gramantieri L, Ventulori L. What is the criterion for differentiating chronic hepatitis from compensated cirrhosis? A
prospective study comparing ultrasonography and percutaneous liver biopsy. J Hepatol. 1997 Dec; 27(6):979-85.
3Ong TZ, Tan HJ. Ultrasonography is not reliable in diagnosing liver cirrhosis in clinical practice. Singapore Med J. 2003
Jun;44(6):293-5.
Where do we stand?
o Ultrasound has a sensitivity of nearly 80%
in diagnosing cirrhosis
Arguedas MR, Heudebert GR, Eloubeidi MA, Abrams GA, Fallon MB. Cost-effectiveness of screening, surveillance,
and primary prophylaxis strategies for esophageal varices. Am J Gastroenterol 2002;97:2441-2452.
Grey-scale ultrasound findings
o Hepatic: Irregular surface, rounded edges,
heterogeneity of texture, nodularity of
substance, shrunken size, volume
redistribution with a dominant left lobe.
o Extrahepatic: splenomegaly, dilated portal
vein, thick walled distended gallbladder,
varices in various locations and ascites.
Liver surface
The diagnosis of cirrhosis by high resolution ultrasound of the liver surface. V Simonovsky.
BJR, 72(199), 29-34
Visceral surface
irregularity
o If anterior surface is difficult to
analyse, look at the deep liver
surface.
o Liver interface at the
gallbladder fossa is easily
accessible for
irregularity. This might
even be more sensitive
Filly RA, Reddy SG, Nalbandian AB, Lu Y. Callen PW. Sonographic evaluation of liver nodularity: Inspection of
deep versus superficial surfaces of the liver. Journal of Clinical Ultrasound Volume 30, Issue 7, pages 399–407,
September 2002
Hepatic vein wall contour
o Hepatic vein contour might
be seen even before any
other feature of cirrhosis
becomes evident
Vessal S, Naidoo S, Hodson J, Stella DL, Gibson RN (2009). Hepatic vein morphology: a new sonographic
diagnostic parameter in the investigation of cirrhosis? J Ultrasound Med 28(9): 1219–1227
Smooth normal
Mildly irregular
Markedly irregular
Texture
Normal
Fatty
Heterogeneous
Other features
Dilated portal vein
Splenomegaly
Thick walled gb
varicesVolume redistribution
Gallbladder wall varices
Coronary vein
Vascular findings
o Dilatation of the portal vein
o Flow disturbances
o Congestion index
o Hepatic artery findings
o Hepatic vein findings
o Splanchnic veins and arteries
o Portosystemic collaterals
The Role of Ultrasonography in Portal Hypertension. Nakshbandi NAA. Saudi Jr.
Gastero.enterol. 2006 12(3):111-117
Vascular findings
o Dilatation of the portal vein
o Flow disturbances
o Congestion index
o Hepatic artery findings
o Hepatic vein findings
o Splanchnic veins and arteries
o Portosystemic collaterals
The Role of Ultrasonography in Portal Hypertension. Nakshbandi NAA. Saudi Jr. Gastero.enterol. 2006
12(3):111-117
Dilatation of the portal vein in
portal hypertension
o Absolute portal vein calibre has been considered a sign of
portal venous hypertension 1 with cutoff values of 13–15
mm. Very poor sensitivity (0.13–0.4). The lack of
sensitivity is likely due to the presence of collateral
pathways that decompress the system and inward stenting
by the fibrous sheath of portal vein 2.
o A small percent of normals have portal vein diameters >13
mm.
1 Weinreb J, Kumari S, Phillips G, Pochaczevsky R (1982) Portal vein measurements
by real-time sonography. AJR Am J Roentgenol. 139(3):497–499
2 Lafortune M, Marleau D, Breton G, Viallet A, Lavoie P, Huet PM (1984) Portal venous
system measurements in portal hypertension. Radiology 151(1):27–30
Portal vein in portal hypertension
Portal vein in portal hypertension
Flow patterns
o Normal portal vein flow
• Continuous, hepatopetal, minimal variation by
cardiac cycle and respiration (pulsatility ratio
<0.54; Pulsatility Index (PI) 0.48+0.31)
o Abnormal portal vein flow
• Continuous but with Increased Pulsatilility
• Respiratory dependent hepatofugal
• Continuous hepatofugal
• Stagnant of no-flow
© Shlomo Gobi, Jerusalem
PV flow
Other vessels (inconsistent
findings)
o Congestion index (pv area/ pv veloctiy; normal
~0.07, cirrhosis when > 0.1)
o Hepatic artery RI can increase with cirrhosis
o Hepatic venous flow velocity can increase due
to compression by nodules and decrease due
increased liver stiffness. Liver stiffness also
alters spectrum and triphasic becomes
monophasic
o Splanchnic veins can dilate
Hepatic vein
Doppler spectra
Portovenous collaterals
o Recanalized paraumbilical veins
o Varices in gallbladder walls
o Coronary:gastro-oesophageal
collaterals behind the left lobe of
the liver
o Collaterals at the splenic hilum;
these can extend above or
below the spleen
o In the pelvic midline or laterally
Varices
Paraumbilical
Splenic hilum
Gallbladder wall varices
Gastro-oesophagial
Anterior abdominal wall
Pelvic
Portal vein thrombosis
o Malignant
• HCC
• Metastatic disease
• Pancreatic carcinoma
• Primary
Leiomyosarcoma of
the portal vein
o Tumour Thrombus
o Benign
• Chronic Pancreatitis
• Appndicitis
• Varicial Injections
• Septicemia
• Trauma
• Splenectomy
• Portacaval shunts
• Pregnancy and other
hypercoagulable states
• Dehydration
• Umbilical vein catheterization
Portal vein thrombosis
Bland thrombi can
resolve/recanalize
Patient had occluding right portal vein thrombus 6 months back
Tumour thrombus
Continuity with mass
Vascularity
PET will discriminate best
Cavernous transformation
Budd Chiari Syndrome
o Occlusion of hepatic veins with or without
ivc occlusion
o Ultrasound features include:
• Ascites, enlarged bulbous liver (acute) with
heterogeneity due to areas of haemorrhagic
infarction
• Caudate lobe enlargement with emissary veins,
occluded hepatic veins and abnormal venous
collaterals
Hepatic vein
thrombosis
Caudate lobe enlargement
and emissary veins
Thank you

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Ultrasound in portal hypertension

  • 1. Ultrasound findings in portal hypertension Durr-e-Sabih MBBS. MS. FRCP. FANMB Director MINAR- Multan PAKISTAN dsabih@yahoo.com
  • 2. Portal hypertension o Normal portal vein pressure is 5-10mm Hg (14 cm H20) o Wedge pressure or direct portal vein pressure >5mm Hg than IVC o Portal vein pressure >30cm H20
  • 3. Portal hypertension Presinusoidal-extrahepatic o Portal and/or splenic vein thrombosis Presinusoidal-intrahepatic o Primary biliary cirrhosis o Schistosomiasis o Congenital Hepatic Fibrosis o Idiopathic noncirrhotic fibrosis o Wilson’s disease o Myelofibrosis o Toxins (Polyvinyl chloride, Methotrexate, arsenic) Sinusoidal o Portal cirrhosis o Sclerosing cholangitis o Diffuse metastatic disease Post sinusoidal o Budd Chiari Syndrome o CCF o Constrictive pericarditis
  • 4. Portal hypertension Presinusoidal-extrahepatic o Portal and/or splenic vein thrombosis Presinusoidal-intrahepatic o Primary biliary cirrhosis o Schistosomiasis o Congenital Hepatic Fibrosis o Idiopathic noncirrhotic fibrosis o Wilson’s disease o Myelofibrosis o Toxins (Polyvinyl chloride, Methotrexate, arsenic) Sinusoidal o Portal cirrhosis o Sclerosing cholangitis o Diffuse metastatic disease Post sinusoidal o Budd Chiari Syndrome o CCF o Constrictive pericarditis
  • 5. Portal hypertension Presinusoidal-extrahepatic o Portal and/or splenic vein thrombosis Presinusoidal-intrahepatic o Primary biliary cirrhosis o Schistosomiasis o Congenital Hepatic Fibrosis o Idiopathic noncirrhotic fibrosis o Wilson’s disease o Myelofibrosis o Toxins (Polyvinyl chloride, Methotrexate, arsenic) Sinusoidal o Portal cirrhosis o Sclerosing cholangitis o Diffuse metastatic disease Post sinusoidal o Budd Chiari Syndrome o CCF o Constrictive pericarditis
  • 6. Where do we stand? o Ultrasound of the liver surface is a useful diagnostic tool in patients at risk of CLD when assessing whether they should undergo a liver biopsy. Meta Analysis, 29 studies.1 o Ultrasound is accurate …and may identify cirrhosis even in the absence of a typical histopathological pattern.2 o Low frequency ultrasonography is not a sensitive test for the diagnosis of liver cirrhosis in daily clinical practice.3 1Allan R, Thoirs K, Phillips M. Accuracy of ultrasound to identify chronic liver disease. World J Gastroenterol. 2010 Jul 28;16(28):3510-20. 2Giani S, Gramantieri L, Ventulori L. What is the criterion for differentiating chronic hepatitis from compensated cirrhosis? A prospective study comparing ultrasonography and percutaneous liver biopsy. J Hepatol. 1997 Dec; 27(6):979-85. 3Ong TZ, Tan HJ. Ultrasonography is not reliable in diagnosing liver cirrhosis in clinical practice. Singapore Med J. 2003 Jun;44(6):293-5.
  • 7. Where do we stand? o Ultrasound has a sensitivity of nearly 80% in diagnosing cirrhosis Arguedas MR, Heudebert GR, Eloubeidi MA, Abrams GA, Fallon MB. Cost-effectiveness of screening, surveillance, and primary prophylaxis strategies for esophageal varices. Am J Gastroenterol 2002;97:2441-2452.
  • 8. Grey-scale ultrasound findings o Hepatic: Irregular surface, rounded edges, heterogeneity of texture, nodularity of substance, shrunken size, volume redistribution with a dominant left lobe. o Extrahepatic: splenomegaly, dilated portal vein, thick walled distended gallbladder, varices in various locations and ascites.
  • 9. Liver surface The diagnosis of cirrhosis by high resolution ultrasound of the liver surface. V Simonovsky. BJR, 72(199), 29-34
  • 10. Visceral surface irregularity o If anterior surface is difficult to analyse, look at the deep liver surface. o Liver interface at the gallbladder fossa is easily accessible for irregularity. This might even be more sensitive Filly RA, Reddy SG, Nalbandian AB, Lu Y. Callen PW. Sonographic evaluation of liver nodularity: Inspection of deep versus superficial surfaces of the liver. Journal of Clinical Ultrasound Volume 30, Issue 7, pages 399–407, September 2002
  • 11. Hepatic vein wall contour o Hepatic vein contour might be seen even before any other feature of cirrhosis becomes evident Vessal S, Naidoo S, Hodson J, Stella DL, Gibson RN (2009). Hepatic vein morphology: a new sonographic diagnostic parameter in the investigation of cirrhosis? J Ultrasound Med 28(9): 1219–1227 Smooth normal Mildly irregular Markedly irregular
  • 13.
  • 14. Other features Dilated portal vein Splenomegaly Thick walled gb varicesVolume redistribution Gallbladder wall varices Coronary vein
  • 15. Vascular findings o Dilatation of the portal vein o Flow disturbances o Congestion index o Hepatic artery findings o Hepatic vein findings o Splanchnic veins and arteries o Portosystemic collaterals The Role of Ultrasonography in Portal Hypertension. Nakshbandi NAA. Saudi Jr. Gastero.enterol. 2006 12(3):111-117
  • 16. Vascular findings o Dilatation of the portal vein o Flow disturbances o Congestion index o Hepatic artery findings o Hepatic vein findings o Splanchnic veins and arteries o Portosystemic collaterals The Role of Ultrasonography in Portal Hypertension. Nakshbandi NAA. Saudi Jr. Gastero.enterol. 2006 12(3):111-117
  • 17. Dilatation of the portal vein in portal hypertension o Absolute portal vein calibre has been considered a sign of portal venous hypertension 1 with cutoff values of 13–15 mm. Very poor sensitivity (0.13–0.4). The lack of sensitivity is likely due to the presence of collateral pathways that decompress the system and inward stenting by the fibrous sheath of portal vein 2. o A small percent of normals have portal vein diameters >13 mm. 1 Weinreb J, Kumari S, Phillips G, Pochaczevsky R (1982) Portal vein measurements by real-time sonography. AJR Am J Roentgenol. 139(3):497–499 2 Lafortune M, Marleau D, Breton G, Viallet A, Lavoie P, Huet PM (1984) Portal venous system measurements in portal hypertension. Radiology 151(1):27–30
  • 18. Portal vein in portal hypertension
  • 19. Portal vein in portal hypertension
  • 20. Flow patterns o Normal portal vein flow • Continuous, hepatopetal, minimal variation by cardiac cycle and respiration (pulsatility ratio <0.54; Pulsatility Index (PI) 0.48+0.31) o Abnormal portal vein flow • Continuous but with Increased Pulsatilility • Respiratory dependent hepatofugal • Continuous hepatofugal • Stagnant of no-flow
  • 21. © Shlomo Gobi, Jerusalem PV flow
  • 22. Other vessels (inconsistent findings) o Congestion index (pv area/ pv veloctiy; normal ~0.07, cirrhosis when > 0.1) o Hepatic artery RI can increase with cirrhosis o Hepatic venous flow velocity can increase due to compression by nodules and decrease due increased liver stiffness. Liver stiffness also alters spectrum and triphasic becomes monophasic o Splanchnic veins can dilate
  • 24. Portovenous collaterals o Recanalized paraumbilical veins o Varices in gallbladder walls o Coronary:gastro-oesophageal collaterals behind the left lobe of the liver o Collaterals at the splenic hilum; these can extend above or below the spleen o In the pelvic midline or laterally
  • 25. Varices Paraumbilical Splenic hilum Gallbladder wall varices Gastro-oesophagial Anterior abdominal wall Pelvic
  • 26. Portal vein thrombosis o Malignant • HCC • Metastatic disease • Pancreatic carcinoma • Primary Leiomyosarcoma of the portal vein o Tumour Thrombus o Benign • Chronic Pancreatitis • Appndicitis • Varicial Injections • Septicemia • Trauma • Splenectomy • Portacaval shunts • Pregnancy and other hypercoagulable states • Dehydration • Umbilical vein catheterization
  • 28. Bland thrombi can resolve/recanalize Patient had occluding right portal vein thrombus 6 months back
  • 29. Tumour thrombus Continuity with mass Vascularity PET will discriminate best
  • 31. Budd Chiari Syndrome o Occlusion of hepatic veins with or without ivc occlusion o Ultrasound features include: • Ascites, enlarged bulbous liver (acute) with heterogeneity due to areas of haemorrhagic infarction • Caudate lobe enlargement with emissary veins, occluded hepatic veins and abnormal venous collaterals

Editor's Notes

  1. Of the many causes we will speak of only a few common ones. These include portal vein thrombosis, Budd Chiari Syndrome and Portal Cirrhosis
  2. Of the few common ones we will address cirrhosis in greatest detail
  3. Most people agree that ultrasound is a useful modality for the initial evaluation of cirrhosis although standard probes and frequencies can have low sensitivity for mild disease
  4. Liver surface irregularities can be easily seen if ascites surrounds the liver. If there is no ascites, and the changes are mild, these might be difficult to see on routine abdominal resolutions and routine convex probes. A high resolution scan of the surface, with the probe held perpendicular to the liver surface will make appreciation of liver surface irregularity easier.
  5. Given the subjective nature of assigning homogeneous or heterogeneous label to liver texture a computer program was developed to aid in this analysis
  6. Of the many vascular findings, dilatation of the portal vein, appearance of collaterals and Doppler changes are the easiest to analyse
  7. Portal vein dilatation is associated with more increased risk of varicial bleed but does not correlate with stage of disease… both patients here have advanced cirrhotic changes but the portal vein is dilated in the patient on the left but normal in the image on right
  8. Pulsatility ratio = minumum velocitiy /maximum velocity. PI = maximum velocity-minimum velocity/ maximum velocity
  9. Normal flow is hepatopetal and constant (15-18cm/sec) with mild respiratory phasicity and very mild cardiac periodicity. As cirrhosis advances, respiratory phasicity is lost, cardiac periodicity can become marked so that the flow becomes almost “arterialized”. The flow velocity can slow down and even reverse or become to-and-fro
  10. Other vessels in the abdomen can show altered flow profiles, but this is not consistent enough or reliable enough to include as a diagnostic sign
  11. Theoretically hepatic venous spectral shape changes from normal triphasic (top) to biphasic (middle) and monophasic (bottom) as liver stiffness increases. Although intellectually very elegant and attractive these changes have rather poor correlation with severity of liver disease
  12. Acute PV thrombus tend to be hypoechoic expansile and avascular, with retraction of clot, there can be re-visualization of flow along the sides or central portions in case of recanalization. Isoechoic thrombi can be difficult to see with grey scale ultrasound
  13. Tumour thorombus can appear identical to a bland thrombus, liver mass points to possible tumour thrombus, tumour extension can be vascular on Doppler and continuity with a mass is highly suggestive. PET scan will show high metabolism in tumour extension and low metabolic activity in bland thrombi
  14. Cavernous transformation generally means a benign process because it takes about 12 months for cavernous channels to appear after portal vein thrombosis.