MalignantSoft tissue
Liposarcoma
Synonyms: Lipomatous sarcoma
Most common STS in adults
Quick Facts
Behaviour
Malignant
Category
Soft tissue
Grade
Variable
Synonyms
Lipomatous sarcoma
Category
Soft tissue
Behaviour
Malignant
Grade
Variable
Gender
M = F
Tissue of Origin
Adipose
Epidemiology
- Most common soft tissue sarcoma in adults
- Peak incidence 40-60 years
- Arises from deep soft tissues, rarely subcutaneous
- Four main subtypes: well-differentiated, myxoid, round cell, pleomorphic
Clinical Features
- Painless mass, often large at presentation
- Rapid growth particularly in myxoid subtype
- Located in deep tHigh, retroperitoneum, chest wall
Location
- Deep tHigh (most common)
- Retroperitoneum
- Chest wall
- Deep Lower extremities
Imaging
- MRI shows fatty lesion with areas of enhancement
- Heterogeneous signal on T2-weighted imaging
- Well-differentiated: predominantly fatty appearance
- Myxoid/round cell: more cellular, increased enhancement
Pathology
- Mature adipocytes with lipoblasts
- Fibrous septa separating fat lobules
- Myxoid stroma in myxoid subtype
- Round cells with increased mitotic activity
Genetics
- t(12;16)(q13;p11) - CHOP gene fusion in myxoid subtype
- Supernumerary ring chromosomes in well-differentiated
Treatment
- Wide surgical excision with negative margins
- Chemotherapy for High-grade and myxoid subtypes
- Radiotherapy for High-grade or unresectable tumours
Prognosis
- Well-differentiated: excellent prognosis with surgery alone
- Myxoid: intermediate prognosis, 5-year survival 60%
- Pleomorphic: poor prognosis, aggressive behaviour
Key Points
- Most common STS in adults
- Subtype determines behaviour and prognosis
- Wide excision is mainstay of treatment
- Follow-up imaging critical for detection of recurrence
Workup - Local Imaging
MRI for local staging
Workup - Biopsy
- Core needle biopsy for diagnosis
- Assess subtype and grade
Workup - Staging
CT CAP
Follow-up Summary
- Years 1–2: 3–4 monthly clinical review + CXR; MRI primary site at 3 months post-op then 6-monthly
- CT chest every 3–4 months for first 2 years (pulmonary metastasis is primary concern)
- Years 3–5: 6-monthly clinical review + CXR; CT chest 6-monthly
- Years 6–10: Annual clinical review + CXR; CT chest annually
- Discharge at 10 years with documented self-monitoring advice
- Radiotherapy patients: monitor irradiated field for late effects at each review