Lipoma
Variant: Myolipoma of Soft Tissue
Lipoleiomyoma of the uterus and cervix is currently classified as a distinct entity
Diagnostic Criteria
- Composed of mature fat and bland smooth muscle
- Muscle predominates in most cases
- Usually evenly interspersed
- Focal smooth muscle overgrowth in one reported case
- Muscle in short fascicles
- Both components lack any atypical features
- No cytologic atypia or lipoblasts
- No floret cells
- No necrosis
- Muscle predominates in most cases
- Stroma may be sclerotic or hyalinized
- Occasionally myxoid
- No prominent vascular component
- Occasional features (none affect behavior)
- Mitotic figures up to 1/10 HPF
- No atypical mitoses
- Focal hypercelllularity of spindle cells
- Degenerative atypia
- Round cell morphology
- Hemosiderin
- Metaplastic cartilage and bone
- Prominent eosinophils
- Mitotic figures up to 1/10 HPF
Supplemental Studies
- Spindle cells positive for smooth muscle actin, desmin, ER
- CD34, HMB45 negative
- HMGA2 60% positive
- MDm2, CDK4 infrequent
Differential Diagnosis
Angiomyolipoma | Myolipoma |
---|---|
Abnormal large vessels | No abnormal vascular component |
Epithelioid perivascular cells | No epithelioid component |
HMB45, MelanA positive | HMB45, MelanA negative |
Atypical Lipomatous Tumor with Smooth Muscle Metaplasia | Myolipoma |
---|---|
Atypical cells present | No atypical cells |
Fibrous septa frequent | Fibrous septa absent |
Floret cells or lipoblasts frequent | No floret cells or lipoblasts |
Spindle Cell Lipoma | Myolipoma |
---|---|
Restricted to back of neck, upper back, shoulders | Predominantly pelvic |
Scant cytoplasm | Tapered cytoplasm in spindle cells |
Ropey collagen frequent | No ropey collagen |
CD34 positive | CD34 negative |
Actin negative | Actin positive |
Low Grade Leiomyosarcoma Infiltrating Fat | Myolipoma |
---|---|
Infiltrative pattern | Circumscribed, encapsulated |
Fat is overrun (asymmetrically involved) | Fat is integral to lesion (throughout) |
May have atypia, mitotic figures | No atypia or mitotic figures rare |
Clinical
- Rarely reported
- Age 28-94
- Vast majority female
- Sites of involvement
- Females: pelvic, retroperitoneal, suprapubic,inguinal
- Males: inguinal, abdominal wall, back
- Other sites include eyelid, spinal cord and pericardium
- No known association with tuberous sclerosis
- No recurrences or metastsis reported
Bibliography
- Takahashi Y, Imamura T, Irie H, Tanaka F, Fukushima J, Fukusato T, Harasawa A, Shiga J. Myolipoma of the retroperitoneum. Pathol Int. 2004 Jun;54(6):460-3.
- Guillou L, Coindre JM. Newly described adipocytic lesions. Semin Diagn Pathol. 2001 Nov;18(4):238-49.
- Michal M. Retroperitoneal myolipoma. A tumour mimicking retroperitoneal angiomyolipoma and liposarcoma with myosarcomatous differentiation. Histopathology. 1994 Jul;25(1):86-8.
- Meis JM, Enzinger FM. Myolipoma of soft tissue. Am J Surg Pathol. 1991 Feb;15(2):121-
- Fukushima, Mana MD; Schaefer, Inga-Marie MD; Fletcher, Christopher D.M. MD, FRCPath.Myolipoma of Soft Tissue: Clinicopathologic Analysis of 34 Cases.
American Journal of Surgical Pathology. 41(2):153-160, February 2017..