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Congenital fibrosarcoma

MONDO:0004557

A fibrosarcoma that occurs in infants. It shares identical morphologic features with adult fibrosarcoma but carries the t(12;15)(p13;q25) translocation that results in ETV6-NTRK3 gene fusion. It usually affects the superficial and deep soft tissues of the extremities. The prognosis is generally much more favorable than for adult fibrosarcoma, and it rarely metastasizes.

Also known as: congenital fibrosarcoma, infantile fibrosarcoma, infantile fibrosarcoma (congenital fibrosarcoma), infantile fibrosarcoma (morphologic abnormality), IFS

2980 clinical trials for this condition and its sub-types, 2 tagged with Congenital fibrosarcoma itself.

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