Lipomas are benign tumors composed of mature adipocytes. They are the most common soft tissue tumor, seen in ~2% of the population.
Patients typically present in adulthood (5-7 decades).
In some cases, multiple lipomas are associated with syndromes and other diseases, including:
- Bannayan-Zonana syndrome
- Cowden syndrome
- Fröhlich syndrome
- Proteus syndrome
- Dercum disease
- Madelung disease
- familial multiple lipomatosis
Typically lipomas are subcutaneous in location and present in adulthood as a soft painless mass in the trunk or proximal extremities. They are likely to have been present for many years and may change size with weight fluctuation.
Benign lipomas are circumscribed soft masses, usually encapsulated, and composed almost entirely of fat. A small amount of non-adipose components are often present, representing fibrous septa, areas of fat necrosis, blood vessels, and interposed muscle fibers. Any non-adipose components must be carefully assessed to exclude a more aggressive component. Histology demonstrates mature adipocytes with no cellular atypia or pleomorphism .
A minority of lipomas are found in deeper locations and include intramuscular, intermuscular, intrathoracic, and retroperitoneal lipomas. These deep lipomatous masses should be assessed carefully, as they are more likely to be malignant. In fact, lesions in retroperitoneal location should be considered a well-differentiated liposarcoma until proven otherwise .
Intramuscular lipomas have nearly identical histology to superficial lipomas; however, intramuscular lesions tend to invade the adjacent musculature and commonly lack a capsule. Thus, these are sometimes known as infiltrating lipoma. In contradistinction, intermuscular lipomas do not exhibit local invasion and tend to be lobular or dumbbell-shaped, easily separated from adjacent soft tissues during surgical resection .
In 5-15% of patients, lipomas are multiple, and approximately a third of these will be familial .
- central nervous system and spine
- head and neck
- breast lipoma
Superficial lipomas are typically well-circumscribed ovoid masses with homogeneous imaging characteristics of fat. A thin capsule, very thin septations (<2 mm), and scattered small areas of soft tissue density are common; however, avidly enhancing, thick/nodular septa or evidence of local invasion are suggestive of malignancy.
Large lipomas may be appreciated as a region of low density exerting mass effect. Calcification may be present in up to 11% of cases, although more commonly associated with well-differentiated liposarcoma .
Lipomas appear as soft variably echogenic masses, commonly encountered on ultrasound. If encapsulated, the capsule may be difficult to identify on ultrasound .
According to a recent study, there is a wide range of appearance of biopsy-proven lipomas, with wide inter-reader variability (2004) :
- hyperechoic: 20-52%
- isoechoic: 28-60%
- hypoechoic: 20%
They also tend to display other ultrasound features, such as :
- no acoustic shadowing
- no or minimal color Doppler flow
Heterogeneous echotexture, more than minimal color Doppler flow, or large size is suspicious for liposarcoma.
Classic appearances are of a superficial circumscribed, low attenuation mass (typically approximately -65 to -120 HU) with minimal internal soft-tissue component. Again, areas of calcification may be present although are more frequently associated with well-differentiated liposarcoma .
Deeper or larger lesions may have scattered areas of internal soft-tissue density, often more apparent on CT versus MRI. These may represent areas of fat necrosis, fibrous tissue, blood vessels, or muscle fibers; these lesions cannot be confidently differentiated from liposarcoma by imaging.
Intramuscular lipomas may invade and interdigitate with the associated skeletal muscle, resulting in a characteristic striated appearance which may help distinguish from liposarcoma .
MRI is the modality of choice for imaging lipomas, not only to confirm the diagnosis, which is usually strongly suggested by ultrasound and CT but also to better assess for atypical features suggesting liposarcoma. Additionally, MRI is better able to demonstrate the surrounding anatomy.
As expected, lipomas follow subcutaneous fat signal on all sequences:
- high signal
- saturates on fat-saturated sequences
- no or minimal enhancement
- high signal on FSE T2
- saturates on fat-saturated sequences: persistent areas of high T2 signal are worrisome
When no suspicious features are present, the diagnosis of lipoma can be made with confidence with MRI being 100% specific . Similarly, if suspicious features are present, then the sensitivity of MRI is 100% , although specificity is lower, as some masses with atypical features will nonetheless be lipomas.
Treatment and prognosis
If all characteristics are those of a simple lipoma, and no local symptoms such as pain are present, then no treatment is generally required. However, resection for cosmesis is also a reasonable indication. If any concern exists, then biopsy or excision is required, with care taken about the approach in case the lesion is malignant. Recurrence rates of 4-5% are reported (most in deeper lesions) .
In general, there is little differential for a classic soft tissue lipoma. The main differential is:
- low-grade tumors are difficult to differentiate from lipomas, and can have a relatively benign clinical course but suffer from high rate of recurrence
- normal adipose tissue
In certain locations, other fatty masses should be considered:
- pleurale Lipome
- intraossäres Lipom
- Myelolipom Nebenniere
- Lipome des Gastrointestinaltraktes
- parosteal lipoma
- lipomatous lesions
- Lipom der Speicheldrüsen
- kardiales Lipom
- tektales Lipom
- ektope Neurohypophyse
- Lipoma arborescens
- parapharyngeal space
- WHO-Klassifikation der Tumoren des zentralen Nervensystems
- Tumoren der Thoraxwand
- WHO Klassifikation der Weichteiltumoren
- subgaleal lipoma
- Leiomyom Ösophagus
- pituitary region mass with intrinsic high T1 signal
- subarachnoid FLAIR hyperintensity
- multiple endokrine Neoplasie Typ 1
- extraskeletal musculoskeletal tumors by compartment
- zerebellopontines Lipom (Lipom im Kleinhirnbrueckenwinkel)
- Lipoleiomyom des Uterus
- Lipom Sonographie
- differential diagnosis for metatarsal region pain
- extra skeletal musculoskeletal lesions by compartment
- Neurofibrom des Ösophagus
- Steatocystoma multiplex
- Lipom versus Liposarkom
- parotid lipoma
- intraosseous lipoma of the parietal bone
- Weichteilschwellung Röntgen
- bannayan zonana syndrome
- low grade liposarcomas (atypical lipomas) of the neck
- Lipom der Thoraxwand
- subcutaneous lipoma of the hand
- Lipom der Harnblase
- parosteal lipoma of the left zygomatic bone
- Lipom mit Fettnekrose
- paravertebral parosteal lipoma
- multiple hepatic lipomas
- nasal encephalocoele
- interkostales Lipom im Muskel
- parosteal lipoma of the femur
- Lipom der Tuba auditiva Eustachii
- pelvine Lipomatose
- Lipom des Fußes
- lipoma of thigh
- thoracic spine lipoma
- knee intra-articular lipoma