Hepatoid tumor
Hepatoid tumor is a rare type of tumor that resembles hepatocellular carcinoma, a type of liver cancer. It can occur in various parts of the body, including the stomach, ovaries, lungs, and pancreas.
Symptoms[edit | edit source]
The symptoms of hepatoid tumor can vary depending on the location of the tumor. Common symptoms may include abdominal pain, weight loss, and jaundice.
Diagnosis[edit | edit source]
Diagnosis of hepatoid tumor is often challenging due to its rarity and the fact that it can mimic other types of tumors. It is typically diagnosed through a combination of imaging studies, biopsy, and blood tests.
Treatment[edit | edit source]
The treatment for hepatoid tumor typically involves surgery to remove the tumor, followed by chemotherapy or radiation therapy. The choice of treatment depends on the size and location of the tumor, as well as the patient's overall health.
Prognosis[edit | edit source]
The prognosis for hepatoid tumor is generally poor, as these tumors are often aggressive and resistant to treatment. However, early detection and treatment can improve the prognosis.
See also[edit | edit source]
References[edit | edit source]
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Contributors: Prab R. Tumpati, MD
