Cholangiosarcoma

Cholangiosarcoma
Synonyms
Pronounce
Specialty	Oncology, Gastroenterology
Symptoms
Complications
Onset
Duration
Types
Causes
Risks
Diagnosis
Differential diagnosis
Prevention
Treatment
Medication
Prognosis
Frequency
Deaths

Cholangiosarcoma is a rare type of cancer that originates in the bile ducts. This malignancy is a form of cholangiocarcinoma, which encompasses all cancers of the bile duct system. The bile ducts are small tubes that carry bile, a fluid produced by the liver to help digest fats, from the liver to the gallbladder and then to the small intestine.

Etiology

The exact cause of cholangiosarcoma is not well understood, but several risk factors have been identified. These include primary sclerosing cholangitis, chronic liver diseases, hepatitis, liver fluke infection (particularly in Southeast Asia), and exposure to certain chemicals such as thorotrast.

Pathophysiology

Cholangiosarcoma arises from the epithelial cells lining the bile ducts. These cells can undergo malignant transformation due to genetic mutations or chronic inflammation, leading to uncontrolled cell growth and tumor formation.

Symptoms

Symptoms of cholangiosarcoma may include jaundice (yellowing of the skin and eyes), abdominal pain, weight loss, and fever. However, symptoms often appear in later stages of the disease, making early diagnosis challenging.

Diagnosis

Diagnosis of cholangiosarcoma involves a combination of imaging studies such as ultrasound, CT scan, and MRI, along with biopsy and histopathological examination of the tissue. Blood tests may also be conducted to check liver function and look for tumor markers.

Treatment

Treatment options for cholangiosarcoma depend on the stage of the disease and may include surgery to remove the tumor, chemotherapy, radiation therapy, and targeted therapy. In some cases, a liver transplant may be considered.

Prognosis

The prognosis for cholangiosarcoma is generally poor, as the cancer is often diagnosed at an advanced stage. The survival rate varies depending on the location of the tumor and the extent of disease at the time of diagnosis.

Epidemiology

Cholangiosarcoma is a rare cancer, with incidence rates varying geographically. It is more common in regions where liver fluke infection is endemic.

See also

• Liver cancer
• Bile duct
• Cancer staging

   This article is a medical stub. You can help WikiMD by expanding it!