Primary Peritoneal Cancer
Primary peritoneal cancer (PPC) is a rare type of cancer that develops in the peritoneum, which is the lining of the abdominal cavity. It is also known as primary peritoneal carcinoma or serous surface papillary carcinoma.
Causes and Risk Factors
The exact cause of primary peritoneal cancer is not known, but several risk factors have been identified. These include:
- Genetic mutations: Women with a family history of breast or ovarian cancer are at increased risk of developing PPC.
- BRCA1 and BRCA2 gene mutations: Women with these genetic mutations are at higher risk of developing PPC, as well as breast and ovarian cancer.
- Age: PPC is more common in postmenopausal women, with most cases diagnosed in women over the age of 50.
Symptoms
The symptoms of primary peritoneal cancer can be non-specific and may include:
- Abdominal bloating or swelling
- Pelvic pain or discomfort
- Weight loss
- Fatigue
- Bowel changes, such as constipation or diarrhea
- Vaginal bleeding or discharge
Diagnosis
Diagnosing primary peritoneal cancer can be challenging, as the symptoms are often similar to those of other conditions. The following tests and procedures may be used to diagnose PPC:
- Pelvic exam: A physical exam to check for any abnormalities in the pelvic area.
- Imaging tests: Such as CT scans, MRI scans, or ultrasound to visualize the abdominal cavity and look for any tumors.
- Blood tests: To check for elevated levels of certain proteins, such as CA-125, which can be a marker for PPC.
- Biopsy: A surgical procedure to remove a sample of tissue from the peritoneum, which is then examined under a microscope for cancer cells.
Treatment
The treatment for primary peritoneal cancer usually involves a combination of surgery and chemotherapy. The goal of treatment is to remove as much of the tumor as possible and to control any remaining cancer cells.
- Surgery: To remove the tumor and any affected tissue, such as the ovaries, fallopian tubes, or uterus.
- Chemotherapy: To kill any remaining cancer cells and prevent the cancer from spreading.
- Targeted therapy: To target specific molecules involved in the growth and spread of cancer cells.
Prognosis
The prognosis for primary peritoneal cancer varies depending on the stage and extent of the disease at diagnosis. Generally, the earlier the cancer is diagnosed and treated, the better the outlook. However, PPC is often diagnosed at an advanced stage, which can make treatment more challenging.
Frequently Asked Questions (FAQs)
What is primary peritoneal cancer?
A rare type of cancer that develops in the peritoneum, a layer of tissue lining the abdominal cavity.
What are the symptoms of primary peritoneal cancer?
Abdominal bloating, pain, and swelling, as well as weight loss and fatigue.
How is primary peritoneal cancer diagnosed?
Through imaging tests, such as CT scans, and biopsy of tissue samples.
What are the risk factors for primary peritoneal cancer?
Genetic mutations, family history, and previous breast or ovarian cancer.
Is primary peritoneal cancer related to ovarian cancer?
Yes, it is similar in characteristics and treatment.
How is primary peritoneal cancer treated?
With surgery, chemotherapy, and sometimes radiation therapy.
What is the prognosis for primary peritoneal cancer?
Generally poor, with a 5-year survival rate of around 10-30%.
Can primary peritoneal cancer be prevented?
No, but risk may be reduced with genetic counseling and screening.
Is primary peritoneal cancer rare?
Yes, it accounts for less than 1% of all female cancers.
What is the typical age range for primary peritoneal cancer diagnosis?
Usually diagnosed in women over 50 years old.
Article last updated on: 25th June 2025.
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