Keywords

These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Definition: A benign tumor constituted by well-differentiated adipocytes.

Epidemiology: The most common among soft tissue tumors. It is more frequently observed between 40 and 60 years of age and prevails in females when it is superficial, whereas in males when it is deep and multiple.

figure a

Localization: (a) Superficial (frequent): in the subcutaneous tissue of the back, shoulder, neck, and proximal extremities. (b) Deep (rare): within or between muscles or adherent to bone, tendons, joints or nerves. In 5 % of cases lipomas are multiple with symmetrical distribution in the dorsum and proximal upper limb.

Clinical: Solitary lump, slow growing, and painless unless there is nerve compression. Superficial lipoma never grows large size (average 4 cm.) and it is movable. Deep lipoma tends to be larger (average 10 cm) and with a spherical, fixed, and firm mass.

Imaging: On X-ray, a radiolucent mass with or without calcification or ossification; mild cortical thickening when parosteal. On CT scan, a lobulated, sharply marginated radiolucency with homogeneous density. On MRI, an encapsulated, bright mass without enhancement after contrast administration; signal intensity equal to that of fat; regular thin septation. On angiography, avascular. On bone scan, there is no uptake.

Histopathology: It is often lobulated with a very thin true capsule and pseudocapsule fibrous, thick, and adherent to the surrounding tissues. Soft on palpation, pale yellow in color, lipoma is constituted by lipocytes, mature “signet ring” cells. Vessels are not very apparent, because they are thin and compressed by lipocytes. On immunohistochemistry, all lipomas are diffusely positive for S-100 and vimentin. Spindle cell and pleomorphic lipoma are also positive for CD34.

Course and Staging: a) Superficial lipoma: easily diagnosed, asymptomatic, generally stage 1, but it may behave as active stage 2 lesion. According to AJC classification, lipoma is more frequently stage Ia. b) Deep lipoma: an extensive anatomo-pathological study with multiple specimens is necessary to exclude liposarcoma lipoma-like. Usually, stage 2 or stage Ib according to AJC classification. Malignant changes are exceptional.

Treatment: Marginal excision is curative. Recurrence is rare (<5 %).

Variants

Age

Sex

Clinical

Gross

Histology

Angiolipoma

20

Male

<2 cm/forearm

Firm

Lipocytes +

Subcutaneous

Yellow/reddish

Network of capillaries with fibrin thrombi

Pain

Spindle cell lipoma

Adult

Male

4 cm/back

Soft

Lipocytes +

Subcutaneous

Yellow/whitish

Vessels + spindle cells +

Painless

Myxoid matrix +

Collagenous bands

Pleomorphic lipoma

Adult

Male

4 cm/back

Firm

Lipocytes +

Subcutaneous

Yellow/whitish

Bizarre floret-like multinucleated cells

Painless

Lipoblastoma

<2

Male

3 cm/limbs

Lobulated translucid

Like myxoid liposarcoma

Subcutaneous

Painless

Lipomatosis

10

Large/diffused

Dense

Mature adipose

Pain

Tissue infiltrating

Intranervous L

<30

Male

Hand/wrist

Hard

Surrounds and infiltrates the nerve

Pain + neuropathy

Hibernoma

Adult

Male

4 cm/scapular

Firm

Central nucleus + Foam cytoplasm = Brown fat

Subcutaneous

Painless

FormalPara Immunohistochemical Panel

Usual Lipoma

VIM

+

S100

+

FormalPara Immunohistochemical Panel

Spindle Cell Lipoma

VIM

+

S100

+

CD34

+

figure b

Mature adipocytic cells organized in lobules with flat nuclei at the periphery and optically empty cytoplasms. No atypia of the cells