CYSTIC DISEASE OF THE LIVER

CHAPTER 7 CYSTIC DISEASE OF THE LIVER




INTRODUCTION


Most hepatic cysts, regardless of type, remain asymptomatic, and hepatic function is not affected. Occasionally cysts are the focus of hemorrhage or infection or produce hepatic dysfunction by bile duct compression or portal hypertension.


This chapter emphasizes open surgical approaches to cystic disease of the liver.



DIAGNOSIS




Computed Tomography


Computed tomographic (CT) features of hepatic cysts are similar to features seen on ultrasound (see Fig 7-3). Cyst hemorrhage and infection are confirmed by intracystic fluid layering or increased density. Vascular enhancement within the cyst wall or mural nodules suggest a cyst-associated malignancy or a cystadenocarcinoma (Fig. 7-4), whereas only septations occur with cystadenoma (Fig. 7-5). Polycystic liver disease (PLD) usually has some component of hepatic venous compression, but ascites usually indicates marked compression of all the major hepatic veins and the retrohepatic inferior vena cava. CT can define the extent of the compression of the major hepatic veins and inferior vena cava and help determine the extent of cyst resection or fenestration required to resolve hepatic venous outflow obstruction.




Magnetic resonance imaging (MRI) should be reserved to address specific issues. If CT fails to define hepatic vasculature accurately, MRI can define the vascular anatomy without contrast media, which may be important in patients with PLD and renal failure.


Endoscopic retrograde cholangiopancreatography (ERCP) documents the site and degree of biliary obstruction or often the site of biliary communication in jaundiced patients. Finally, cholangiography is essential to differentiate bile duct cysts from hepatic cysts with biliary communication. Magnetic resonance cholangiopancreatography (MRCP) also can be used for definition of the biliary system.



SIMPLE CYSTS


Simple cysts may be solitary or multiple, but they are usually unilocular. Simple cysts rarely have true septations but frequently have intrahepatic portal pedicles, which traverse a portion of the cyst periphery, which may mimic septa. Simple cysts do not communicate with the biliary tree. The content of simple cysts is usually serous but can be bile stained, mucoid, bloody, or turbid and thick, The adjacent liver may become compressed and atrophic, and there may be compression of the adjacent portal pedicles.


Symptoms develop insidiously and include abdominal fullness or pressure, satiety, and mild dyspnea from cyst expansion and compression of adjacent organs. Sharp pain may follow intracystic hemorrhage. Cyst infection is associated with fever and rigors. Jaundice may accompany extensive compression of the bile duct confluence or common hepatic duct but is very rare. Liver function is almost always normal.


The indications for treatment of simple cysts are symptoms or associated complications. Simple cysts may be complicated by hemorrhage, infection, rupture into the peritoneal cavity or into the biliary tree or adjacent bowel, jaundice, and very rarely portal hypertension. Aspiration should never be used as a sole definitive treatment because cyst recurrence is certain.



TREATMENT


Currently the choice of treatment for simple cysts includes aspiration and sclerosis, laparoscopic excision or fenestration, and excision or fenestration at laparotomy.




May 30, 2016 | Posted by in GASTOINESTINAL SURGERY | Comments Off on CYSTIC DISEASE OF THE LIVER

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