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juxtacortical osteosarcoma - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

juxtacortical osteosarcoma

MONDO:0006817

Also known as:juxtacortical osteogenic sarcomaparosteal osteogenic sarcomaparosteal osteosarcoma

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Overview

A low grade malignant bone-forming mesenchymal neoplasm arising from the surface of the bone. It usually affects the distal posterior femur, the proximal tibia, and proximal humerus. Painless swelling is the usual clinical sign. Most patients are young adults and the prognosis is usually excellent.

Clinical Trials1 registered

Diagnosis

Biomarker and diagnostic research for juxtacortical osteosarcoma 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.

1 clinical trial registered. Interventions under study include other interventions. Research is primarily sponsored by academic and government institutions.

16 publications have been identified in PubMed for juxtacortical osteosarcoma. Research spans Case Report / Case Series (38%), Diagnostic / Biomarker (19%), and Review / Meta-Analysis (19%).

Research Type	Count	% of Total
Patient case studies	6	38%

Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 3:47 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

Questions for Your Care Team

→Are any of the 1 active clinical trial 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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juxtacortical osteosarcoma

Overview

Diagnosis

Research Landscape

Medical References

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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