Cholangiocarcinoma: Everything You Need To Know

| health

Cholangiocarcinoma: Everything You Need To Know

 

Cholangiocarcinoma is a type of cancer that affects the bile ducts. It can be a difficult and complex disease to treat, but with the right information and resources, it can be managed. In this article, we'll discuss all you need to know about Cholangiocarcinoma - its symptoms, diagnosis, treatment for Cholangiocarcinoma, and more. So if you have been recently diagnosed with this condition or are just curious to learn more about it, read on!

 

What is Cholangiocarcinoma?


Cholangiocarcinoma is a type of cancer that starts in the cells of the bile ducts. The bile ducts are tubes that carry bile from the liver to the small intestine. Bile is a fluid that helps with digestion. Cholangiocarcinoma can occur in anyone, but it is more common in people over age 60. It is also more common in men than women.

There are two types of cholangiocarcinoma:

 

Intrahepatic


Intrahepatic means the cancer starts inside the liver.

 

Extrahepatic


Extrahepatic means it starts outside the liver, in the part of the bile duct that goes through the pancreas or duodenum (the first part of the small intestine).

Most cholangiocarcinomas are adenocarcinomas, which start in glandular (secretory) cells. There are other types of cholangiocarcinoma, such as sarcomas, which start in connective tissue cells, and hepatoblastomas, which start in liver cells. These other types are much less common than adenocarcinomas.

 

Causes of Cholangiocarcinoma


Cholangiocarcinoma can either be primary, which means it originates in the bile ducts, or secondary, which means it has spread from another cancerous tumor.

There are several potential causes of cholangiocarcinoma, including:

  • Infection with certain viruses or bacteria, such as Hepatitis B or C

  • Exposure to certain toxins, such as those found in some insecticides and herbicides

  • Inflammation of the bile ducts (primary sclerosing cholangitis)

  • Cirrhosis of the liver

  • Genetic disorders such as familial adenomatous polyposis and hereditary hemorrhagic telangiectasia


While the exact cause of cholangiocarcinoma is often unknown, these are some of the most likely culprits. If you have any risk factors for this disease, it’s important to speak with your doctor so you can be monitored closely.

 

Symptoms of Cholangiocarcinoma


The bile ducts are tubes that carry bile from the liver to the small intestine. Bile is a yellowish-green fluid that helps with digestion.

Most people with cholangiocarcinoma do not have any symptoms in the early stages of the disease. When symptoms do occur, they may include:

  • Jaundice (yellowing of the skin and whites of the eyes)

  • Itching

  • Fatigue

  • Weight loss

  • Loss of appetite

  • Nausea and vomiting

  • Abdominal pain or bloating

  • Fever


If the cancer is found early, surgery may be an option. However, cholangiocarcinoma often spreads quickly and is difficult to treat. Chemotherapy and radiation therapy may help to control the symptoms, but they are usually not successful in curing the disease.

 

Risk Factors for Cholangiocarcinoma


Cholangiocarcinoma, or bile duct cancer, is a rare and aggressive form of cancer that develops in the bile ducts. The bile ducts are the tubes that carry bile from the liver to the small intestine. Cholangiocarcinoma can develop in anyone, but there are certain risk factors that may increase your chances of developing this type of cancer.

Some of the most common risk factors for cholangiocarcinoma include:

  • A history of chronic inflammation or infection of the bile ducts (chronic cholecystitis or cholangitis)

  • A history of gallstones

  • Liver cirrhosis

  • Primary sclerosing cholangitis (PSC) – a condition that causes inflammation and scarring of the bile ducts

  • Familial polyposis syndromes – genetic conditions that cause numerous polyps to form in the lining of the colon and other parts of the digestive tract


If you have any of these risk factors, it’s important to speak with your doctor so they can monitor your health closely.

 

Diagnosis and Treatment of Cholangiocarcinoma


Cholangiocarcinoma is a type of cancer that starts in the cells lining the bile ducts. Bile ducts are tubes that carry bile from the liver to the small intestine. Cholangiocarcinoma can occur in any part of the biliary system, including the:

 

Intrahepatic bile ducts:


These are the bile ducts within the liver.

 

Extrahepatic bile ducts:


These are the bile ducts outside of the liver, including the common hepatic duct, cystic duct, and common bile duct.

 

Peripheral cholangiocarcinoma:


This type of cholangiocarcinoma starts in the gallbladder or other parts of the biliary system.

The most common symptom of cholangiocarcinoma is jaundice, which is when your skin and whites of your eyes turn yellow. Other symptoms include itching, dark urine, pale stools, weight loss, and fatigue.

If you have any of these symptoms, it’s important to see your doctor right away. Cholangiocarcinoma is often diagnosed with imaging tests such as CT scan or MRI. A biopsy may also be done to confirm the diagnosis.

Once cholangiocarcinoma is diagnosed, treatment options will be based on several factors including the stage of cancer and

 

Conclusion


It can be difficult to diagnose, but early detection and treatment are key to improving outcomes. Cholangiocarcinoma often requires aggressive treatments such as surgery, chemotherapy, and radiation therapy. Knowing the signs and symptoms of this cancer can help raise awareness for people who may be at risk or have been diagnosed with cholangiocarcinoma. With continued research, better options for detection and treatment will become available in order to improve patient outcomes. In case, you are diagnosed with Cholangiocarcinoma, must book an appointment with a hepatologist for proper treatment.

Join our newsletter

We’ll send you a nice letter once per week. No spam.

Please enter valid email address