Pediatric Li-Fraumeni Syndrome (LFS)

What is Pediatric Li-Fraumeni Syndrome (LFS)?

Li-Fraumeni syndrome (LFS) is a hereditary (runs in families) condition in which several people across multiple generations develop various types of cancer, and they are typically diagnosed at a young age (under 30).

A person may be diagnosed with LFS when all of the following are true:

• Develops a sarcoma (rare cancer that grows in connective tissue) before age 45
• Has a first-degree relative (parent, sibling or child) who is diagnosed with any cancer before age 45
• Has a first- or second-degree (grandparent, aunt, uncle, niece, nephew or grandchild) who is diagnosed with any cancer before age 45 or with a sarcoma at any age

The most common types of cancers found in families with LFS are:

• Acute leukemia
• Adrenal cortical tumors
• Brain cancer
• Breast cancer
• Osteosarcoma (bone cancer)
• Soft-tissue sarcoma

What are the signs and symptoms of Pediatric Li-Fraumeni Syndrome (LFS)?

Since LFS is a condition that increases the chance of cancer, children with this conditions should watch for signs of cancer, such as:

• Frequent headaches or changes in vision
• Loss of appetite or unexplained weight loss
• Lumps or swelling of the skin
• Unexplained aches and pains