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PORTAL VEIN THROMBOSIS

63 yr male with multiple well defined round
to oval shaped lesions with variable sizes
studding the Rt lobe of the liver ( especially   MERCURY IMAGING
the segment 6 and 7 of the liver ) .                INSTITUTE
The echo pattern of these lesions is
heterogeneous – primarily Hyperechoic at         SCO 172-173 SEC 9C
places. The largest of all the lesions              CHANDIGARH
measures 53mmx 48mmx 56mm in size (
seen in the segment 6/7 of the liver ) . Note    MERCURY IMAGING CENTRE
is made of prominent main portal vein with       SCO 16-17 SEC 20D
intraluminal thrombus in the main portal
vein extending to the left and Rt branches          CHANDIGARH
also . Periportal collaterals are appreciated
on color Doppler.
Dilated main portal vein with intraluminal thrmobus
with intermediate to hyperechoic echopattern suggestive of
                subacute stage thrombus .
Serpigenous tracts along the periphery of
the intraluminal thrombus – ? Partially patent lumen / recanallization..
Thrombus extending to the left main branch and more
      vertically oriented left lobe branches .
Serpigenous tracts along the periphery of
the intraluminal thrombus – ? Partially patent lumen / recanallization..
PORTAL VEIN THROMBOSIS
         ETIOLOGY :                          BRIEF ANATOMY :
• Reduced portal blood flow caused    • Generally, the portal vein enters
  by hepatic parenchymal disease        the porta hepatis and divides into
  and abdominal sepsis                  the right and left main branches.
  (ie, infectious or ascending          The right main branch divides
  thrombophlebitis) are the major       into anterior and posterior
  causes.                               branches that supply the anterior
• Transient PVT is also being           and posterior segments of the
  recognized with abdominal             right lobe. The left main branch
  inflammation such as appendicitis     courses horizontally to the left
• Hypercoagulable syndromes can         before turning vertically to form
  lead to portomesenteric and           the medial and lateral segmental
  splenic vein thrombosis.              branches.
Points to remember................
• Tumor in the portal vein may         • In children, the portal vein may
  have an appearance identical to        recanalize with the development
  that of thrombosis, but this           of multiple, small, collateral
  appearance is far less common          channels. These channels are seen
  than others. Tumor in the portal       as a partly echogenic band of small
  vein is most frequently related to     vessels extending to the porta
  HCC.The thrombus may be partial        hepatis (cavernous
  or complete. It may be mixed           transformation). These have a
  with bland thrombus as well.           reduced flow velocity of 2-7 cm/s.
• Adults who have acute PVT              Nonvisualization of the portal vein
  secondary to abdominal sepsis          is strongly suggestive of occlusion.
  may completely recover, and the        The portal vein may then be seen
  vessel may recanalize with             as a band of high-level echoes at
  successful treatment of the            the porta hepatis.
  underlying sepsis.
RADIOGRAPH

                     • Hepatosplenomegaly
CONVENTIONAL
RADIOGRAPHS CAN      • Enlarged azygos vein.
HELP TO ASSESS THE
FOLLOWING            • Para spinal varices .
OBSERVATIONS …….
USG
                                              •   PVT eliminates the usual venous flow signal
                                                  from the lumen of the portal vein during
                                                  either pulsed or color flow Doppler imaging.
•   On sonograms, echogenic lesions               Color flow Doppler images can show flow
    may be present in the portal vein.            around a thrombus that partially blocks the
    Clot with variable echogenicity may           vein. However, if flow is sluggish, the Doppler
    be depicted. The clot usually has             signal may not be detected. Color flow may
                                                  be present in other small collateral vessels.
    moderate echogenicity, but if it is       •   Incomplete occlusion may occur. This is
    recently formed, it may be                    common with neoplastic invasion.
    hypoechoic. Patent vessels may                Alternatively, thrombolytic recanalization
    have increased intraluminal                   may occur. The two cannot be differentiated
                                                  on sonograms. Cavernous malformation,
    echogenicity because of                       spontaneous shunts, and splenorenal and
    erythrocyte rouleaux formation,               portosystemic collaterals may be seen. The
    which makes slow-flowing blood                underlying cause (eg, hepatocellular
    slightly echogenic. Increased or              carcinoma, metastases, cirrhosis, pancreatic
                                                  neoplasms) may be evident. The incidence of
    decreased echogenicity may be                 PVT is reported to be low in portal
    observed in the lumen of the portal           hypertension.
    vein. In isolation, this finding is not   •   The string sign—that is, thickening of the
    sufficient to diagnose or exclude             portal vein with narrowing of its lumen—is
    PVT.                                          assumed to be caused by portal phlebitis.
                                                  This is considered a precursor of PVT in
                                                  patients with acute pancreatitis. The portal
                                                  vein thrombus may be calcified. The
                                                  diameter of the portal vein is larger than 15
                                                  mm in 38% of the cases of PVT.
CT
•   On contrast-enhanced CT scans, PVT may be •         The portal vein supplies 75% of the
    depicted as a low-attenuating center in the         blood flow to the liver. Therefore,
    portal vein surrounded by peripheral                peak liver contrast enhancement
    enhancement. Portal vein attenuation is 20-         occurs during the portal venous
    30 HU less than that of the aorta.                  phase, about 60 seconds after the
•   CT angiography (CTA) is an application of           start of a bolus injection of contrast
    helical CT. The rapidity of helical CT allows the   material.With helical CT, a liver
    maintenance of a higher concentration of            examination requires about 20
    intravenous contrast medium, particularly           seconds to complete; images can
    through the arterial enhancement phase, and
    it has the capability of 3-dimensional (3D)         usually be acquired in one breath
    reconstruction. Both peripheral intravenous         hold.[18]
    injections of contrast agent and CT arterial •      This technique can be extended to
    portography have been used as with CTA. CTA         acquire a dual-phase contrast-
    has shown great promise in the evaluation of        enhanced CT scan in which the liver
    hepatic vessels before liver resection. It          is imaged twice with a single
    provides preoperative surgical information          contrast agent bolus, first during
    about the segmental location of liver tumors,
    the segmental venous anatomy, and the               the arterial phase and then through
    presence of significant arterial anomalies. The     portal venous phase. Dual-phase CT
    value of CTA in the evaluation of portal            is indicated in some cases involving
    hypertension is unclear, but CTA is likely to be    benign or malignant lesions in
    useful because it may delineate the collateral      which vascular characteristics
    vessels, varices, and other findings in patients    suggest the correct diagnosis (see
    with portal hypertension.                           the images below).
MRI
•   The vascular anatomy of the liver may be     •   MRCP coupled with dynamic 3D
    outlined by using spin-echo and gradient-        gradient-echo imaging can not
    recalled-echo (GRE) techniques, but these        only detect portal vein occlusion,
    techniques cannot demonstrate the
    direction of portal flow. Time-of-flight MRI     cavernous transformation, and
    with bolus tracking has been successful in       gallbladder varices but also depict
    the assessment of portal hypertension and        bile duct abnormalities associated
    its squeal. Phase-contrast sequences can         with portal biliopathy.
    also be used to evaluate the portal
    vein, and phase-contrast cine MRA can
    show the direction of portal venous flow
    and the presence of portal vein thrombus.
    Magnetic resonance evaluation of the
    portal venous system accurately
    demonstrates thrombosis and the
    collateral circulation. Gadolinium
    enhancement is useful in this application
    (see the images below).

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Portal vein thrombosis

  • 1. PORTAL VEIN THROMBOSIS 63 yr male with multiple well defined round to oval shaped lesions with variable sizes studding the Rt lobe of the liver ( especially MERCURY IMAGING the segment 6 and 7 of the liver ) . INSTITUTE The echo pattern of these lesions is heterogeneous – primarily Hyperechoic at SCO 172-173 SEC 9C places. The largest of all the lesions CHANDIGARH measures 53mmx 48mmx 56mm in size ( seen in the segment 6/7 of the liver ) . Note MERCURY IMAGING CENTRE is made of prominent main portal vein with SCO 16-17 SEC 20D intraluminal thrombus in the main portal vein extending to the left and Rt branches CHANDIGARH also . Periportal collaterals are appreciated on color Doppler.
  • 2. Dilated main portal vein with intraluminal thrmobus with intermediate to hyperechoic echopattern suggestive of subacute stage thrombus .
  • 3. Serpigenous tracts along the periphery of the intraluminal thrombus – ? Partially patent lumen / recanallization..
  • 4. Thrombus extending to the left main branch and more vertically oriented left lobe branches .
  • 5. Serpigenous tracts along the periphery of the intraluminal thrombus – ? Partially patent lumen / recanallization..
  • 6. PORTAL VEIN THROMBOSIS ETIOLOGY : BRIEF ANATOMY : • Reduced portal blood flow caused • Generally, the portal vein enters by hepatic parenchymal disease the porta hepatis and divides into and abdominal sepsis the right and left main branches. (ie, infectious or ascending The right main branch divides thrombophlebitis) are the major into anterior and posterior causes. branches that supply the anterior • Transient PVT is also being and posterior segments of the recognized with abdominal right lobe. The left main branch inflammation such as appendicitis courses horizontally to the left • Hypercoagulable syndromes can before turning vertically to form lead to portomesenteric and the medial and lateral segmental splenic vein thrombosis. branches.
  • 7. Points to remember................ • Tumor in the portal vein may • In children, the portal vein may have an appearance identical to recanalize with the development that of thrombosis, but this of multiple, small, collateral appearance is far less common channels. These channels are seen than others. Tumor in the portal as a partly echogenic band of small vein is most frequently related to vessels extending to the porta HCC.The thrombus may be partial hepatis (cavernous or complete. It may be mixed transformation). These have a with bland thrombus as well. reduced flow velocity of 2-7 cm/s. • Adults who have acute PVT Nonvisualization of the portal vein secondary to abdominal sepsis is strongly suggestive of occlusion. may completely recover, and the The portal vein may then be seen vessel may recanalize with as a band of high-level echoes at successful treatment of the the porta hepatis. underlying sepsis.
  • 8. RADIOGRAPH • Hepatosplenomegaly CONVENTIONAL RADIOGRAPHS CAN • Enlarged azygos vein. HELP TO ASSESS THE FOLLOWING • Para spinal varices . OBSERVATIONS …….
  • 9. USG • PVT eliminates the usual venous flow signal from the lumen of the portal vein during either pulsed or color flow Doppler imaging. • On sonograms, echogenic lesions Color flow Doppler images can show flow may be present in the portal vein. around a thrombus that partially blocks the Clot with variable echogenicity may vein. However, if flow is sluggish, the Doppler be depicted. The clot usually has signal may not be detected. Color flow may be present in other small collateral vessels. moderate echogenicity, but if it is • Incomplete occlusion may occur. This is recently formed, it may be common with neoplastic invasion. hypoechoic. Patent vessels may Alternatively, thrombolytic recanalization have increased intraluminal may occur. The two cannot be differentiated on sonograms. Cavernous malformation, echogenicity because of spontaneous shunts, and splenorenal and erythrocyte rouleaux formation, portosystemic collaterals may be seen. The which makes slow-flowing blood underlying cause (eg, hepatocellular slightly echogenic. Increased or carcinoma, metastases, cirrhosis, pancreatic neoplasms) may be evident. The incidence of decreased echogenicity may be PVT is reported to be low in portal observed in the lumen of the portal hypertension. vein. In isolation, this finding is not • The string sign—that is, thickening of the sufficient to diagnose or exclude portal vein with narrowing of its lumen—is PVT. assumed to be caused by portal phlebitis. This is considered a precursor of PVT in patients with acute pancreatitis. The portal vein thrombus may be calcified. The diameter of the portal vein is larger than 15 mm in 38% of the cases of PVT.
  • 10. CT • On contrast-enhanced CT scans, PVT may be • The portal vein supplies 75% of the depicted as a low-attenuating center in the blood flow to the liver. Therefore, portal vein surrounded by peripheral peak liver contrast enhancement enhancement. Portal vein attenuation is 20- occurs during the portal venous 30 HU less than that of the aorta. phase, about 60 seconds after the • CT angiography (CTA) is an application of start of a bolus injection of contrast helical CT. The rapidity of helical CT allows the material.With helical CT, a liver maintenance of a higher concentration of examination requires about 20 intravenous contrast medium, particularly seconds to complete; images can through the arterial enhancement phase, and it has the capability of 3-dimensional (3D) usually be acquired in one breath reconstruction. Both peripheral intravenous hold.[18] injections of contrast agent and CT arterial • This technique can be extended to portography have been used as with CTA. CTA acquire a dual-phase contrast- has shown great promise in the evaluation of enhanced CT scan in which the liver hepatic vessels before liver resection. It is imaged twice with a single provides preoperative surgical information contrast agent bolus, first during about the segmental location of liver tumors, the segmental venous anatomy, and the the arterial phase and then through presence of significant arterial anomalies. The portal venous phase. Dual-phase CT value of CTA in the evaluation of portal is indicated in some cases involving hypertension is unclear, but CTA is likely to be benign or malignant lesions in useful because it may delineate the collateral which vascular characteristics vessels, varices, and other findings in patients suggest the correct diagnosis (see with portal hypertension. the images below).
  • 11. MRI • The vascular anatomy of the liver may be • MRCP coupled with dynamic 3D outlined by using spin-echo and gradient- gradient-echo imaging can not recalled-echo (GRE) techniques, but these only detect portal vein occlusion, techniques cannot demonstrate the direction of portal flow. Time-of-flight MRI cavernous transformation, and with bolus tracking has been successful in gallbladder varices but also depict the assessment of portal hypertension and bile duct abnormalities associated its squeal. Phase-contrast sequences can with portal biliopathy. also be used to evaluate the portal vein, and phase-contrast cine MRA can show the direction of portal venous flow and the presence of portal vein thrombus. Magnetic resonance evaluation of the portal venous system accurately demonstrates thrombosis and the collateral circulation. Gadolinium enhancement is useful in this application (see the images below).