Chorioblastoma
Chorioblastoma
Chorioblastoma, also known as choriocarcinoma, is a rare and aggressive type of cancer that develops from trophoblastic cells, which are cells that normally form the placenta during pregnancy. This type of cancer most commonly occurs in the uterus, but it can also develop in the ovaries, testes, or other parts of the body.
Symptoms[edit | edit source]
Symptoms of chorioblastoma may include abnormal vaginal bleeding, pelvic pain, and an enlarged uterus. In some cases, the cancer may spread to other parts of the body, leading to symptoms such as shortness of breath, chest pain, and neurological symptoms.
Diagnosis[edit | edit source]
Diagnosis of chorioblastoma is typically made through a combination of imaging tests, such as ultrasound and CT scans, as well as blood tests to measure levels of certain hormones. A biopsy of the affected tissue is often necessary to confirm the diagnosis.
Treatment[edit | edit source]
Treatment for chorioblastoma usually involves a combination of surgery, chemotherapy, and radiation therapy. Surgery may be performed to remove the cancerous tissue, while chemotherapy and radiation therapy are used to kill any remaining cancer cells and prevent the cancer from spreading.
Prognosis[edit | edit source]
The prognosis for chorioblastoma depends on various factors, including the stage of the cancer at the time of diagnosis and the patient's overall health. With early detection and prompt treatment, many patients with chorioblastoma can achieve remission and live cancer-free.
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Contributors: Prab R. Tumpati, MD