Indication
Liposarcoma
Liposarcoma is a rare malignant soft-tissue sarcoma that originates in adipocytic precursor cells. Read more about Liposarcoma
15 drugs 14 manufacturers
Drugs that treat it
Common Liposarcoma therapies.
YONDELIS (trabectedin)
ERIBULIN MESYLATE
ERIBULIN MESYLATE
ERIBULIN MESYLATE
ERIBULIN MESYLATE
ERIBULIN MESYLATE
ERIBULIN MESYLATE
ERIBULIN MESYLATE
News & literature
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Coming soonLiposarcoma is a rare malignant soft-tissue sarcoma that originates in adipocytic precursor cells.
It predominantly affects adults, most frequently developing in the deep soft tissues of the retroperitoneum and the extremities, particularly the thigh.
Pathophysiologically and histologically, the disease encompasses distinct subtypes, including well-differentiated, dedifferentiated, myxoid/round cell, and pleomorphic variants, which are defined by variable degrees of lipoblastic differentiation, cytogenetic abnormalities such as *MDM2* and *CDK4* gene amplification or characteristic chromosomal translocations, and clinical behavior that ranges from locally indolent to aggressively metastatic.
Clinically, it typically presents as an enlarging, painless deep-tissue mass that produces compressive symptoms as it expands into adjacent structures.
- cancer.gov
Liposarcoma is a rare malignant soft-tissue sarcoma that originates in adipocytic precursor cells It predominantly affects adults, most frequently developing in the deep soft tissues of the retroperitoneum and the extremities, particularly the thigh Pathophysiologically and histologically, the disease encompasses distinct subtypes, including well-differentiated, dedifferentiated, myxoid/round cell, and pleomorphic variants, which are defined by variable degrees of lipoblastic differentiation, cy...
- childrenshospital.org
Liposarcoma is a rare malignant soft-tissue sarcoma that originates in adipocytic precursor cells It predominantly affects adults, most frequently developing in the deep soft tissues of the retroperitoneum and the extremities, particularly the thigh Pathophysiologically and histologically, the disease encompasses distinct subtypes, including well-differentiated, dedifferentiated, myxoid/round cell, and pleomorphic variants, which are defined by variable degrees of lipoblastic differentiation, cy...
- nih.gov
Pathophysiologically and histologically, the disease encompasses distinct subtypes, including well-differentiated, dedifferentiated, myxoid/round cell, and pleomorphic variants, which are defined by variable degrees of lipoblastic differentiation, cytogenetic abnormalities such as *MDM2* and *CDK4* gene amplification or characteristic chromosomal translocations, and clinical behavior that ranges from locally indolent to aggressively metastatic
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