History and exam

Key diagnostic factors

common

presence of risk factors

Key risk factors include a genetic predisposition due to familial multiple lipomatosis, Gardner's syndrome, or Bannayan-Riley-Ruvalcaba's syndrome.

cutaneous mass <5 cm diameter

Most extremity or truncal lipomas are <5 cm in diameter. The majority of liposarcomas present at a size >5 cm. Studies suggest that a size of 10 cm or larger is a strong discriminating feature for liposarcoma.[20] Definitive diagnosis is dependent on histological confirmation.[16]​​

soft cutaneous mass

Lipomas tend to be soft and doughy in texture, similar to the consistency of subcutaneous fat. A firm texture may indicate liposarcoma. A smooth but tense superficial lesion may represent an epidermoid cyst.

mobile cutaneous mass

Most cutaneous lipomas are mobile. If a lesion appears fixed or tethered to the underlying fascia, a liposarcoma should be ruled out using imaging and biopsy.

superficial cutaneous mass

Most cutaneous lipomas are superficial. If a lesion seems deep to the superficial fascia, imaging should be considered to rule out liposarcoma.[16]​​

Other diagnostic factors

uncommon

painless cutaneous mass

Most lipomas are painless but can cause some discomfort if they undergo abrasion from clothing. Angiolipomas, which tend to be multiple and occur in young adults, can sometimes be painful to touch. Chronic pain is present in Dercum's disease but not in lipomatosis.

gastrointestinal obstruction

Lipomas occur as submucosal lesions in the gastrointestinal (GI) tract, most commonly in the stomach, small intestine, and colon. Rarely these may present with intestinal obstruction.[7][29][38]​​​​​​

gastrointestinal bleeding

Lipomas occur as submucosal lesions in the GI tract most commonly in the stomach, small intestine, and colon. Rarely these may present with GI bleeding.[7][29][38]​​​​​​

Risk factors

strong

genetic predisposition

The hereditary condition of familial multiple lipomatosis is characterised by multiple lipoma development.[9]​​[10]​​ Patients with this autosomal condition tend to be male and have widespread symmetric lipomas of the extremities and trunk.​[11] Lipomatosis may also be associated with Madelung's disease, Dercum's disease, and Gardner's syndrome.[21]​​ Studies have shown a correlation between HMG 1-C gene mutation and lipoma development.[22]​​

weak

trauma

Although trauma is implicated as a potential inciting agent, it is unclear whether it is a true causal factor.[27]​​[28]​​

heavy alcohol consumption

Madelung's disease, also known as multiple symmetric lipomatosis, features benign symmetric lipomatosis of the head, neck, shoulders, and proximal upper extremities. It is more common in men and is associated with chronic alcohol consumption in genetically predisposed individuals.​[13]

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