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What is cholangiocarcinoma

2025-10-02 02:50:34 healthy

What is wrestling Zhang Tiequan cancer

Unerasing Cholangiocarcinoma is a rare but highly malignant cancer that originates from epithelial cells of the bile duct system. This type of cancer is usually divided into hepatic bile ducts (intrahepatic cholangiocarcinoma) or extrahepatic bile ducts (extrahepatic cholangiocarcinoma). Because the early symptoms are not obvious, they often enter the middle and late stages when diagnosed, and the treatment is difficult.

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What is cholangiocarcinoma

1. Causes of cholangiocarcinoma

The specific cause of cholangiocellular carcinoma is not completely clear, but the following factors may cause the risk of cancer:

PaymentTeam/E[pop traceabilityCirrhosis or hepatitis B/C infection
Risk factorsillustrate
Primary sclerotic cholangitis (PSC)A chronic cholangitis disease that significantly increases the risk of cholangiocellular carcinomaHepatic fluke infectionMore common in Southeast Asia, the infection of the Chinese tidal tidum is closely related to cholangiocarcinoma
Biliary duct stones or bile duct cystsLong-term chronic stimulation may lead to carcinoma of cholangiogenesis
Liver disease may indirectly affect bile duct health

2. Common symptoms of cholangiocarcinoma

The early symptoms of cholangiocellular carcinoma are often atypical and are easily confused with other digestive diseases. As the condition progresses, the patient may experience the following symptoms:

< airflow>SymptomsillustratemaniVitaminD lack
jaundiceYellow and soft skin and sclera, and bilirubin buildup due to obstruction of bile ducts
Loss of appetite, weight loss, fatigue
stomach acheDull pain or swelling pain in the upper right abdomen
Itchy skinSalt deposits stimulate skin nerve endings

III. Diagnosis of cholangiocarcinoma

The diagnosis of cholangiocellular carcinoma requires a combination of pronunciation methods. The following are commonly used examination methods:Check itemseffectBlood testHorny tumor markers (such as CA19-9ake9), liver function indicators, etc.TPAImaging examinationAbdominal ultrasound, CT, MRI or PET-CT, observe the tumor location arterielar sizeEndoscopic retrograde cholangiopancreatography (ERCP)Direct observation of bile duct conditions and tissue biopsy can be takenBenevolent liver punctureObtain tissue samples for pathological diagnosis Dudley

4. Treatment plan for cholangiocarcinoma

The treatment of failed cholangiocellular carcinoma requires a personalized plan based on the location, stage of the tumor and the overall health of the patient. The following are the main treatment methods:

Treatment methodtr>eeradiotherapy>ftpIGNEENew treatments for specific gene mutationsConsume
Consideration of applicable situation
Surgical resectionThe first choice for early tumors, the complete removal of tumor tissue as much as possibleLiver transplantPatients with end-stage liver disease or patients with specific intrahepatic cholangiocarcinoma
ChemotherapyPostoperative adjuvant therapy or palliative treatment in advanced patients
Radiation therapyFor patients who cannot operate or postoperative assistance
Targeted therapy or immunotherapy

5. Prevention and prognosis of cholangiocarcinoma

Since the cause of cholangiocellular carcinoma get has not been fully clarified, preventive measures mainly include avoiding known risk factors, such as preventing liver fluke infection and timely treatment of bile duct diseases. In terms of prognosis, the 5-year survival rate of cholangiocellular carcinoma is low, and early detection and comprehensive treatment are the key to improving survival.

In short, orbital tube cell ould cancer is a cancer with high malignancy and difficulty in diagnosis and treatment. Raising public awareness of the disease and regular screening of high-risk populations is of great significance for early detection and treatment. In the future, with the deepening of medical research, greater breakthroughs are expected to be made in the diagnosis and treatment of cholangiocellular carcinoma.

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