Abdomino-Pelvic Sarcoma

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EA 3.4 Abdomino-Pelvic Sarcoma

Abdomino-pelvic sarcoma is a rare type of cancer that develops in the soft tissue of the abdomen and pelvis. Soft tissue sarcomas are a group of cancers that arise from the tissues that support and connect the body, such as muscle, fat, and connective tissue. Abdomino-pelvic sarcomas are typically slow-growing tumours that can be difficult to diagnose because they often do not cause symptoms until they are quite large. Common symptoms of this type of cancer may include abdominal pain, bloating, a feeling of fullness, and unexplained weight loss. The exact cause of abdomino-pelvic sarcoma is unknown, but certain risk factors have been identified, including a family history of soft tissue sarcoma, exposure to radiation therapy, and certain genetic conditions. Diagnosis of abdomino-pelvic sarcoma usually involves imaging tests, as well as a biopsy to examine a sample of the tumour tissue. Treatment for this type of cancer may include surgery to remove the tumour, radiation therapy, and chemotherapy. The choice of treatment depends on the size and location of the tumour, as well as the patient’s overall health and personal preferences.