Biloma

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Duodenobiliary fistula of biliary tree. Duodeno Biliary Fistula 08786.jpg
Duodenobiliary fistula of biliary tree.

A biloma is a circumscribed abdominal collection of bile outside the biliary tree. [1] It occurs when there is excess bile in the abdominal cavity. It can occur during or after a bile leak. There is an increased chance of a person developing biloma after having a gallbladder removal surgery, known as laparoscopic cholecystectomy. This procedure can be complicated by biloma with incidence of 0.3–2%. [2] Other causes are liver biopsy, abdominal trauma, and, rarely, spontaneous perforation. The formation of biloma does not occur frequently. Biliary fistulas are also caused by injury to the bile duct and can result in the formation of bile leaks. Biliary fistulas are abnormal communications between organs and the biliary tract. [3] Once diagnosed, they usually require drainage. The term "biloma" was first coined in 1979 by Gould and Patel. [4] [5] They discovered it in a case with extrahepatic bile leakage. The cause of this was trauma to the upper right quadrant of the abdomen. Originally, biloma was described as an "encapsulated collection" of extrahepatic bile. Biloma is now described as extrabiliary collections of bile that can be either intrahepatic or extrahepatic. The most common cause of biloma is trauma to the liver. There are other causes such as abdominal surgery, endoscopic surgery and percutaneous catheter drainage. [6] Injury and abdominal trauma can cause damage to the biliary tree. The biliary tree is a system of vessels that direct secreations from the liver, gallbladder, and pancreas through a series of ducts into the duodenum. This can result in a bile leak which is a common cause of the formation of biloma. It is possible for biloma to be associated with mortality, though it is not common. Bile leaks occur in about one percent of causes. [1]

Contents

Signs and symptoms

Symptoms include diffused or localized abdominal pain without a fever. A blood test will show leukocytosis and nonspecific liver test abnormalities. [7] Symptoms of Biloma can range from severe to having no symptoms at all. If a patient presents with no symptoms, this event makes them nonspecific. Other symptoms can range from abdominal pain, distention, jaundice, and fever. Fevers are usually due to leukocytosis being present. Physical examination revealed epigastric fullness and right upper quadrant discomfort. This is usually the result of a disruption of the bile tree. In a case of infected biloma, the symptoms would include nausea, vomiting, and fever. [1]

Patients may present with acute symptoms, no symptoms or a wide range of symptoms. This makes diagnosing biloma challenging. Early signs of biloma after traumatic injury include persistent abdominal distention, bloating, and/or anorexia. Patients who have undergone hepatobiliary surgery or laparoscopic cholecystectomy are more at risk for developing biloma. [8] Consequently, these patients should be observed more frequently so it does not turn into an infection.

Etiology

Research and diagnosis have proven that bilomas are secondary to biliary obstruction. This process is caused by trauma or iatrogenic procedures. Iatrogenic cases are procedures such as laparoscopic cholecystectomy, endoscopic retrograde cholangiopancreatography (ERCP), radiofrequency ablation (RFA), liver transplant, resection, and biopsy." [1]

Pathophysiology

Leakage of bile and destruction of the biliary tree are the most common causes of biloma. Destruction of the billary tree means that there is a blockage in the pancreatic or bile duct. Bile ducts are vessels that carry from the liver to the gallbladder. When bile becomes blocked, pancreatic juices cannot be transported to the intestines. Bile leakage causes inflammation in abdominal tissues or liver parenchyma. This results in fibrosis and encapsulation. Bile leakage is located at the biliary tube site with rare occurrences at the anastomotic site. [1] Greenish-yellow bile is usually present as well as blood. This will occur if there is an infection present. Infections can lead to sepsis, abscess formation and inflammatory response.

Diagnosis

Diagnosis includes abdominal ultrasounds. A wide range of symptoms makes the diagnosis of biloma difficult. Delayed diagnosis 77% of patients resulted from abdominal bile collections and bile leaks after a laparoscopic cholecystectomy. [1] Radiographic imaging is used to diagnose and confirm bile leaks. Imaging also determines if it is extrahepatic or intrahepatic. A radiographic image will also show to what extent the bile leak is. A computerized tomography (CT) is also used to diagnose biloma. CT scans will show fluid collection in the right upper quadrant of the abdomen.In order to localize the leak, CT intravenous cholangiography can be used to show the communication between the biliary tree and the biloma. Magnetic resonance imaging (MRI) will demonstrate signaling intensity on T1-weighted imaging, and signaling intensity on T2-weighted imaging. [9] This means that there is a fluid build up. [9]

Treatment

Severity of the condition will determine treatment options. Depending on the severity of the case of biloma, they will be treated differently. Laboratory and radiological findings of biloma will help in determining the overall treatment plan. There are several treatments for biloma. Treatments are symptom dependent and include endoscopic drainage, surgical drainage, or close monitoring. In asymptomatic situations, fluid collections can be reabsorbed and can be closely monitored without intervention.

Considering that biloma is a rare complication, most studies on successful treatment are derived from case reports. 150 cases of biloma have been reported and treated. [10] Radiologically guided percutaneous drainage is also a successful treatment option. However, in the result of a failed drainage of biloma, surgery would be the next option. Due to draining being the best and preferred method of treatment, patients usually have a very good prognosis.

Prognosis

There are several factors that will affect the prognosis of biloma. This includes: size, site and the etiology which can be described as the cause. Although prognosis still depends on size, site and etiology, patients usually recover. Cases of asymptomatic bilomas respond well to treatment. This means that there were no complications and the bile leak was successfully managed. In cases of symptomatic patients, those who had interventional radiology drainage have a successful prognosis. Drainage via interventional radiology prevents infection and improves patient morbidity and mortality. [8]

Due to most bilomas being treated with percutaneous drainage, biloma will not recur or present with infection resulting in a good prognosis. There are instances in larger bile leaks where leaks into the peritoneum result in morbidity. [1]

Epidemiology

Due to the limited research and cases presented of biloma, there is little known of its epidemiology. Cases usually present in patients of 60 to 70 years of age. In majority of diagnosed cases, they are secondary to iatrogenic disruption of the biliary tree. This means the incidence of biloma will depend on the frequency of intervention. To date, there has not been a difference between men and women who have a formation of biloma. In the case of spontaneous biloma, they rarely form. All studies on spontaneous cases of biloma cases are from case reports dating 2007, which stated that 27 cases of spontaneous bilomas had been reported since 1979. [11]

Research directions

There was a study conducted from 2007 to 2017. The purpose of the study was to determine which method of treatment is most successful given a case of biloma. First the study determined that most biliary leaks resulted from cholecystectomy (27%) and hepatectomy (50%). [12] In the study, endoscopic pseudocyst drainage was performed, which is a technique used to drain fluid. There was a clinical success rate of 70.4% in the group of patients. [12]

The study concluded that the most successful treatment option is endoscopic pseudocyst drainage. The study states that using this technique will eliminate the need for surgery even in patients with complex cases.

See also

Related Research Articles

<span class="mw-page-title-main">Gallbladder</span> Organ in humans and other vertebrates

In vertebrates, the gallbladder, also known as the cholecyst, is a small hollow organ where bile is stored and concentrated before it is released into the small intestine. In humans, the pear-shaped gallbladder lies beneath the liver, although the structure and position of the gallbladder can vary significantly among animal species. It receives and stores bile, produced by the liver, via the common hepatic duct, and releases it via the common bile duct into the duodenum, where the bile helps in the digestion of fats.

<span class="mw-page-title-main">Bile duct</span> Type of organ

A bile duct is any of a number of long tube-like structures that carry bile, and is present in most vertebrates. The bile duct is separated into three main parts the fundus, body, and neck which are superior, middle, and inferior respectively.

<span class="mw-page-title-main">Cholecystitis</span> Inflammation of the gallbladder

Cholecystitis is inflammation of the gallbladder. Symptoms include right upper abdominal pain, pain in the right shoulder, nausea, vomiting, and occasionally fever. Often gallbladder attacks precede acute cholecystitis. The pain lasts longer in cholecystitis than in a typical gallbladder attack. Without appropriate treatment, recurrent episodes of cholecystitis are common. Complications of acute cholecystitis include gallstone pancreatitis, common bile duct stones, or inflammation of the common bile duct.

<span class="mw-page-title-main">Caroli disease</span> Medical condition

Caroli disease is a rare inherited disorder characterized by cystic dilatation of the bile ducts within the liver. There are two patterns of Caroli disease: focal or simple Caroli disease consists of abnormally widened bile ducts affecting an isolated portion of liver. The second form is more diffuse, and when associated with portal hypertension and congenital hepatic fibrosis, is often referred to as "Caroli syndrome". The underlying differences between the two types are not well understood. Caroli disease is also associated with liver failure and polycystic kidney disease. The disease affects about one in 1,000,000 people, with more reported cases of Caroli syndrome than of Caroli disease.

<span class="mw-page-title-main">Cholecystectomy</span> Surgical removal of the gallbladder

Cholecystectomy is the surgical removal of the gallbladder. Cholecystectomy is a common treatment of symptomatic gallstones and other gallbladder conditions. In 2011, cholecystectomy was the eighth most common operating room procedure performed in hospitals in the United States. Cholecystectomy can be performed either laparoscopically, or via an open surgical technique.

<span class="mw-page-title-main">Common bile duct stone</span> Medical condition

Common bile duct stone, also known as choledocholithiasis, is the presence of gallstones in the common bile duct (CBD). This condition can cause jaundice and liver cell damage. Treatments include choledocholithotomy and endoscopic retrograde cholangiopancreatography (ERCP).

<span class="mw-page-title-main">Gallbladder cancer</span> Medical condition

Gallbladder cancer is a relatively uncommon cancer, with an incidence of fewer than 2 cases per 100,000 people per year in the United States. It is particularly common in central and South America, central and eastern Europe, Japan and northern India; it is also common in certain ethnic groups e.g. Native American Indians and Hispanics. If it is diagnosed early enough, it can be cured by removing the gallbladder, part of the liver and associated lymph nodes. Most often it is found after symptoms such as abdominal pain, jaundice and vomiting occur, and it has spread to other organs such as the liver.

<span class="mw-page-title-main">Cholestasis</span> Medical condition

Cholestasis is a condition where the flow of bile from the liver to the duodenum is impaired. The two basic distinctions are:

An accessory bile duct is a conduit that transports bile and is considered to be supernumerary or auxiliary to the biliary tree.

<span class="mw-page-title-main">Biliary fistula</span> Medical condition

A biliary fistula is a type of fistula in which bile flows along an abnormal connection from the bile ducts into a nearby hollow structure. Types of biliary fistula include:

<span class="mw-page-title-main">Ascending cholangitis</span> Medical condition

Ascending cholangitis, also known as acute cholangitis or simply cholangitis, is inflammation of the bile duct, usually caused by bacteria ascending from its junction with the duodenum. It tends to occur if the bile duct is already partially obstructed by gallstones.

<span class="mw-page-title-main">Biliary tract</span> Organ system

The biliary tract refers to the liver, gallbladder and bile ducts, and how they work together to make, store and secrete bile. Bile consists of water, electrolytes, bile acids, cholesterol, phospholipids and conjugated bilirubin. Some components are synthesized by hepatocytes ; the rest are extracted from the blood by the liver.

<span class="mw-page-title-main">Percutaneous transhepatic cholangiography</span> Medical imaging of the biliary tract

Percutaneous transhepatic cholangiography, percutaneous hepatic cholangiogram (PTHC) is a radiological technique used to visualize the anatomy of the biliary tract. A contrast medium is injected into a bile duct in the liver, after which X-rays are taken. It allows access to the biliary tree in cases where endoscopic retrograde cholangiopancreatography has been unsuccessful. Initially reported in 1937, the procedure became popular in 1952.

<span class="mw-page-title-main">Choledochal cysts</span> Medical condition

Choledochal cysts are congenital conditions involving cystic dilatation of bile ducts. They are uncommon in western countries but not as rare in East Asian nations like Japan and China.

Biliary injury is the traumatic damage of the bile ducts. It is most commonly an iatrogenic complication of cholecystectomy, but can also be caused by other operations or by major trauma. The risk of biliary injury is higher during laparoscopic cholecystectomy than during open cholecystectomy. Biliary injury may lead to several complications and may even cause death if not diagnosed in time and managed properly. Ideally biliary injury should be managed at a center with facilities and expertise in endoscopy, radiology and surgery.

Secondary sclerosing cholangitis (SSC) is a chronic cholestatic liver disease. SSC is a sclerosing cholangitis with a known cause. Alternatively, if no cause can be identified, then primary sclerosing cholangitis is diagnosed. SSC is an aggressive and rare disease with complex and multiple causes. It is characterized by inflammation, fibrosis, destruction of the biliary tree and biliary cirrhosis. It can be treated with minor interventions such as continued antibiotic use and monitoring, or in more serious cases, laparoscopic surgery intervention, and possibly a liver transplant.

<span class="mw-page-title-main">Sphincter of Oddi dysfunction</span> Medical condition

Sphincter of Oddi dysfunction refers to a group of functional disorders leading to abdominal pain due to dysfunction of the Sphincter of Oddi: functional biliary sphincter of Oddi and functional pancreatic sphincter of Oddi disorder. The sphincter of Oddi is a sphincter muscle, a circular band of muscle at the bottom of the biliary tree which controls the flow of pancreatic juices and bile into the second part of the duodenum. The pathogenesis of this condition is recognized to encompass stenosis or dyskinesia of the sphincter of Oddi ; consequently the terms biliary dyskinesia, papillary stenosis, and postcholecystectomy syndrome have all been used to describe this condition. Both stenosis and dyskinesia can obstruct flow through the sphincter of Oddi and can therefore cause retention of bile in the biliary tree and pancreatic juice in the pancreatic duct.

Cholecystostomy or (cholecystotomy) is a medical procedure used to drain the gallbladder through either a percutaneous or endoscopic approach. The procedure involves creating a stoma in the gallbladder, which can facilitate placement of a tube or stent for drainage, first performed by American surgeon, Dr. John Stough Bobbs, in 1867. It is sometimes used in cases of cholecystitis or other gallbladder disease where the person is ill, and there is a need to delay or defer cholecystectomy. The first endoscopic cholecystostomy was performed by Drs. Todd Baron and Mark Topazian in 2007 using ultrasound guidance to puncture the stomach wall and place a plastic biliary catheter for gallbladder drainage.

<span class="mw-page-title-main">Choledochoduodenostomy</span>

Choledochoduodenostomy (CDD) is a surgical procedure to create an anastomosis, a surgical connection, between the common bile duct (CBD) and an alternative portion of the duodenum. In healthy individuals, the CBD meets the pancreatic duct at the ampulla of Vater, which drains via the major duodenal papilla to the second part of duodenum. In cases of benign conditions such as narrowing of the distal CBD or recurrent CBD stones, performing a CDD provides the diseased patient with CBD drainage and decompression. A side-to-side anastomosis is usually performed.

<span class="mw-page-title-main">Biliary endoscopic sphincterotomy</span> Use of endoscopy and fluoroscopy to treat and diagnose digestive issues.

Biliary endoscopic sphincterotomy is a procedure where the sphincter of Oddi and the segment of the common bile duct where it enters the duodenum are cannulated and then cut with a sphincterotome, a device that includes a wire which cuts with an electric current (electrocautery).

References

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