Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Jendrik Hardes, Georg Gosheger, Timo Budny

    Zeitschrift Fur Orthopadie Und Unfallchirurgie
    |February 23, 2018
    PubMed
    Summary
    This summary is machine-generated.

    Bone sarcomas are rare cancers often misdiagnosed due to vague symptoms. Early radiographic examination and interdisciplinary care in specialized centers are crucial for optimal outcomes in treating these rare bone tumors.

    Related Concept Videos

    You might also read

    Related Articles

    Articles linked to this work by shared authors, journal, and citation graph.

    Sort by
    Same author

    Fast fix or false hope? Polyethylene exchange in unstable primary unconstrained total knee arthroplasty.

    Bone & joint open·2026
    Same author

    Durable mid-term survivorship after proximal ACL repair with suture augmentation in a middle-aged cohort: A risk factor analysis.

    Journal of experimental orthopaedics·2026
    Same author

    A modified Delphi consensus on tenosynovial giant cell tumour and giant cell tumour of bone : a report from the Birmingham Orthopaedic Oncology Meeting (BOOM).

    The bone & joint journal·2026
    Same author

    Complications of PI to PIII hemipelvic resections for intermediate and malignant tumours : a systematic review and meta-analysis.

    Bone & joint open·2026
    Same author

    Treatment effect heterogeneity of radiotherapy in localized Ewing sarcoma: A secondary analysis of the EURO-E.W.I.N.G. 99 and Ewing 2008 trial.

    European journal of cancer (Oxford, England : 1990)·2026
    Same author

    Diagnostic Accuracy of Synovial Calprotectin in Megaprosthetic Reconstructions: A Prospective Cohort Study from a Tertiary Sarcoma Center.

    Cancers·2026
    Same journal

    Chronic Osteomyelitis - Pathophysiology and Treatment.

    Zeitschrift fur Orthopadie und Unfallchirurgie·2026
    Same journal

    Posterior Malleolus Fractures of the Tibia: Open Reduction and Buttress Plating versus Percutaneous Fixation with an Anteroposterior Screw.

    Zeitschrift fur Orthopadie und Unfallchirurgie·2026
    Same journal

    Ultrasound Assessment of Talar, Femoral and Metacarpal Cartilage Thicknesses in Hemiplegic Patients and their Relationship with Functional Parameters.

    Zeitschrift fur Orthopadie und Unfallchirurgie·2026
    Same journal

    Current Concepts in Acute and Chronic Lateral Ankle Instability.

    Zeitschrift fur Orthopadie und Unfallchirurgie·2026
    Same journal

    Zeitschrift fur Orthopadie und Unfallchirurgie·2026
    Same journal

    Zeitschrift fur Orthopadie und Unfallchirurgie·2026
    See all related articles

    Area of Science:

    • Orthopedics
    • Oncology
    • Radiology

    Background:

    • Bone sarcomas are rare, accounting for ~0.2% of all cancers.
    • Vague initial symptoms like pain or limping can lead to delayed diagnosis.
    • Common types include osteosarcoma, chondrosarcoma, and Ewing sarcoma, with varying age predilections.

    Purpose of the Study:

    • To highlight the challenges in diagnosing and treating rare bone sarcomas.
    • To emphasize the importance of early radiographic evaluation for unexplained symptoms.
    • To advocate for an interdisciplinary approach and centralized treatment in specialized centers.

    Main Methods:

    • Review of common bone sarcoma types, demographics, and locations.
    • Description of standard treatment modalities including surgery, chemotherapy, and radiation therapy.

    Related Experiment Videos

  • Emphasis on the necessity of limb-sparing surgery and reconstruction techniques.

    • Main Results:

    • Osteosarcomas and Ewing sarcomas predominantly affect younger individuals, while chondrosarcomas are more common in older patients.
    • Most bone sarcomas occur in extremities and pelvis, with ~90% amenable to limb-sparing surgery.
    • Multimodal therapy (surgery, chemotherapy, radiation) is standard for osteosarcoma and Ewing sarcoma.

    Conclusions:

    • An interdisciplinary approach involving multiple specialists is vital for accurate diagnosis and effective treatment.
    • Centralized management in specialized sarcoma centers improves patient prognosis and functional outcomes.
    • Regular follow-up is essential for detecting recurrences of these rare bone tumors.