Lipoma arborescens (LA) is a rare synovial disorder characterized by the replacement of subsynovial tissue with mature fat cells, often termed villous lipomatous proliferation of the synovium (
1,
2). The suprapatellar pouch is almost always the affected site, with or without the lateral recesses of the knee joint (
2,
3). Very rare cases in the wrist, elbow, shoulder, hip, and ankle have been reported, as well as an even smaller number of bilateral and polyarticular cases (
4). LA equally affects males and females most often the 5
th to 7
th decades of life, though age range reaches as low as 9 years (
2,
4). The most common associated pathology is joint effusion, followed by degenerative changes, meniscal tear, synovial cyst, bone erosion, and synovial chondromatosis (
2,
4). Hypothesized etiologies of LA include traumatic, inflammatory, rheumatologic, developmental, and reactive processes (
1,
4). The disorder can be classified into primary type that exists without associated joint changes and is more common in younger patients, and secondary type that occurs in the setting of degenerative joint disease and is more common in older patients (
4).