Liver: The liver was subjectively subnormal in size with atrophy of the right liver lobes. The capsule contour was smooth. There was subjectively decreased vascularity in the liver. The PV:CVC:AO ratio is a normal 1:1:1 in the extra-hepatic region, ruling out a EHPSS. On examination of the intra-hepatic branching of the portal vein, the central and left divisional branches appear normal, and thus can be ruled out as a cause of intrahepatic shunting. However, the right divisional branch of the portal vein lacks the normal narrowing/branching shape and may be connecting with the vena cava. This consists of a short connection at the level of the diaphragm. This would need to be evaluated and potentially confirmed with CT with contrast.
Kidneys: Both kidneys were mildly swollen in contour and potentially increased in size. The capsule contour was smooth with no deviation. The internal architecture was normal. There was no pelvic dilation. The left kidney measured 5 in length. The right kidney measured 5.5 cm in length.
Bladder: The bladder contained minimal amounts of urine, primarily anechoic with mild echogenic suspended sediment. There was a 1 cm strongly shadowing hyperechoic density in the bladder. There may be a second area of strongly shadowing sediment towards the trigone/urethra.
Ultrasound diagnosis
Liver: Suspected right divisional intra-hepatic portosystemic shunt (IHPSS) Subjectively subnormal liver size, particularly the right liver.
Kidney: Bilateral renomegaly – suspect swelling secondary to IHPSS.
Bladder: Bladder stone/s or conglomeration of mineralized sand.
CT image interpretation
Liver: The portal vein presents a normal order of its tributary veins. Originating from the right lateral intrahepatic branch of the portal vein, a short anomalous connection is seen, draining into a right hepatic vein. The anomalous vascular connection is measuring 6.8 mm in diameter.
Kidneys: Both kidneys present an increased volume. After contrast administration a bilaterally symmetric and uniform nephro- and pyelogram is noted.
CT diagnosis
Liver: Right divisional intrahepatic portosystemic shunt.
Kidneys: Renomegaly.
Case status 8/25/2023
The findings from the CT study are consistent with a congenital single intrahepatic portosystemic shunt originating from the right lateral intrahepatic branch of the portal vein, presenting as a short anomalous vascular connection. Hepatic encephalopathy is a potential cause for the neurological clinical signs. Slow progressive closure technique (coil, ameroid) is the therapy of choice. Empirical treatment until functional shunt closure along with feeding of a hepatic diet is recommended.
Case update
fill with update