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liposarcoma

Epidemiology: ~20% of adulthood sarcomas [2] Pathology: Microscopic pathology: Identification of lipoblasts which range from: 1) primitive mesenchymal cells with only tiny lipid droplets 2) intermediate form with scanty cytoplasm, multiple variably sized lipid droplets and small nucleus centrally or peripherally located 3) signet-ring like cells with most of cytoplasm occupied by single large fat droplet Histologic subtypes: 1) well-differentiated liposarcoma (atypical lipoma/atypical lipomatous tumor) a) lipoma like b) sclerosing c) inflammatory d) spindle cell e) dedifferentiated 2) myxoid liposarcoma a) round cell liposarcoma 3) pleomorphic liposarcoma * histopathology images [4] Genetics: - implicated genes PRUNE

Interactions

disease interactions

Specific

dedifferentiated liposarcoma myxoid liposarcoma pleomorphic liposarcoma round cell liposarcoma well-differentiated liposarcoma; atypical lipomatous tumor; sclerosing liposarcoma; inflammatory liposarcoma; spindle cell liposarcoma

General

adipose tissue neoplasm soft tissue sarcoma (STS)

References

  1. Enzinger & Weiss. Soft Tissue Tumors. Mosby. 3rd ed. 1995
  2. Gebhard et al. Am J Surgical Pathology 26:601-16, 2002
  3. DermNet NZ. Lipoma and liposarcoma (images) http://www.dermnetnz.org/lesions/lipoma.html
  4. DermNet NZ. Liposarcoma pathology (histopathology images) http://www.dermnetnz.org/pathology/liposarcoma-path.html
  5. Schwartz RA, Elston DM (CT image) Medscape: Liposarcoma http://emedicine.medscape.com/article/1102007-overview