Hepatocellular carcinoma (HCC), also called hepatoma, is one of the most common types of liver cancer. People who have a history of liver ailments such as Hepatitis B or alcohol abuse are likely to develop this type of cancer.
Hepatocellular carcinoma is a type of liver cancer that is grown in hepatocytes. Men are more at risk of developing hepatoma, as compared to women. In most cases of HCC, individuals do not experience any symptoms. The symptoms individuals may have are related to cirrhosis.
Fibrolamellar carcinoma
Fibrolamellar carcinoma, also called FLC, is a subtype of hepatocellular cancer. It is a rare type of cancer that is usually developed in teens and individuals under 40 years of age. The one thing that makes this type of liver cancer different is that it is developed in individuals with healthy livers.
Most other liver cancers are developed in people who have liver ailments or liver damage because of infections or drug abuse. In the initial stage of liver cancer, an individual may not experience any symptoms.
When cancer progresses to advanced stages, individuals may experience jaundice, loss of appetite, nausea, abdomen pain, back pain, or weakness.
To diagnose liver cancer, your doctor may recommend you doing imaging tests and biopsy. Fibrolamellar carcinoma is treated with the help of chemotherapy, embolisation therapy, and surgeries.
Cholangiocarcinoma
Cholangiocarcinoma is also called bile duct cancer. This is one of the types of cancer occurs in the bile ducts, a long tube-like structure that connects your liver to the gallbladder and small intestine.
Individuals older than 50 years of age are more likely to get cholangiocarcinoma. Signs and symptoms of cholangiocarcinoma include jaundice, stools that are white in color, weakness, itching, pain in the abdomen, and sudden weight loss.
Angiosarcoma
Angiosarcoma is one of the types of liver cancer that is extremely rare and is formed in the blood vessels of the liver and lymph vessels. This is also known as haemangiosarcoma or soft tissue sarcoma. Individuals with a history of radiation therapy are more likely to get angiosarcoma.
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