Sarcopedia

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