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Liposarcoma in children and young adults: a multi-institutional experience
Winston W Huh1, Carrie Yuen, Mark Munsell
1Division of Pediatrics, University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA. whuh@mdanderson.org
Pediatric Blood & Cancer
|March 12, 2011
Summary
Pediatric liposarcoma differs from adult types, with myxoid subtypes showing excellent outcomes and pleomorphic subtypes having poor prognoses. Adjuvant radiotherapy
Area of Science:
- Pediatric Oncology
- Surgical Pathology
- Radiation Oncology
Background:
- Limited data exist on pediatric liposarcoma clinical presentation and outcomes compared to adults.
- The efficacy of adjuvant radiotherapy in childhood liposarcoma treatment remains unclear.
Purpose of the Study:
- To investigate differences in clinical presentation and outcomes of liposarcoma between pediatric and adult patients.
- To evaluate the role of adjuvant radiotherapy in pediatric liposarcoma treatment.
Main Methods:
- A multi-institutional retrospective analysis of medical records was conducted for patients aged 21 years or younger with a confirmed liposarcoma diagnosis.
- Data on patient demographics, tumor subtype, location, treatment, and outcomes were collected and analyzed.
Main Results:
- Thirty-three pediatric patients were analyzed; 24 had myxoid and 7 had pleomorphic liposarcoma.
- Myxoid liposarcomas predominantly occurred in extremities with no metastases and showed excellent prognosis, with only one death from progressive disease after multimodal therapy.
- Pleomorphic liposarcomas occurred in axial sites, and despite multimodal therapy, 6 out of 7 patients relapsed, with 4 deaths from progressive disease.
Conclusions:
- Pediatric liposarcoma exhibits distinct presentation and outcomes compared to adult cases.
- Myxoid liposarcoma is the common pediatric subtype, presenting in extremities with a favorable prognosis.
- Pleomorphic liposarcoma in children has a poor prognosis, necessitating further research into optimal therapeutic strategies.

