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congenital fibrosarcoma - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

congenital fibrosarcoma

MONDO:0004557

Also known as:infantile fibrosarcomainfantile fibrosarcoma (congenital fibrosarcoma)infantile fibrosarcoma (morphologic abnormality)

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Overview

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.

Clinical Trials2 registered

Diagnosis

Biomarker and diagnostic research for congenital fibrosarcoma has been reported in the published literature.

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

2 clinical trials registered. Interventions under study include drug therapy. Pipeline includes 1 PHASE2, 1 PHASE1. Research is sponsored by a mix of industry and academic institutions.

58 publications have been identified in PubMed for congenital fibrosarcoma. Research spans Case Report / Case Series (48%), Review / Meta-Analysis (16%), and Basic Science / Preclinical (12%).

Research Type	Count	% of Total
Patient case studies	28	48%

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 12:30 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

Questions for Your Care Team

→Are any of the 2 active clinical trials a good fit for my situation?
→Are there specialists or centers of excellence for this condition in my area?
→Is there a patient registry I should consider joining?

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congenital fibrosarcoma

Overview

Diagnosis

Research Landscape

Medical References

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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