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

[Rhabdomyosarcoma in children].

A F Bukhny, B M Belkina, V M Blinov

    Voprosy Onkologii
    |January 1, 1990
    PubMed
    Summary

    Pediatric rhabdomyosarcoma diagnosis and treatment present challenges. Survival rates vary significantly by tumor location, with head and neck sites showing lower two-year survival.

    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

    Viral component of the human genome.

    Molecular biology·2020
    Same author

    [Viral component of the human genome].

    Molekuliarnaia biologiia·2017
    Same author

    [Ovarian germ cell tumors in girls].

    Voprosy onkologii·2015
    Same author

    [Mechanisms of retroviral immunosuppressive domain-induced immune modulation].

    Molekuliarnaia biologiia·2014
    Same author

    [Cell analogs of viral proteins].

    Zhurnal mikrobiologii, epidemiologii i immunobiologii·2014
    Same author

    [Combined use conventional and videoendosurgery in pediatric oncology].

    Vestnik Rossiiskoi akademii meditsinskikh nauk·2012

    Area of Science:

    • Pediatric Oncology
    • Surgical Oncology
    • Radiation Oncology

    Context:

    • Rhabdomyosarcoma is a rare but aggressive soft tissue sarcoma in children.
    • Accurate diagnosis and multimodal treatment are crucial for improving outcomes.
    • This study analyzes diagnostic and therapeutic strategies in a cohort of pediatric patients.

    Purpose:

    • To evaluate the diagnostic challenges and treatment outcomes for pediatric rhabdomyosarcoma.
    • To identify factors influencing survival rates based on tumor location and treatment modalities.
    • To provide insights into optimizing the management of this pediatric malignancy.

    Summary:

    • A study of 198 pediatric rhabdomyosarcoma patients revealed common tumor sites in genitourinary organs (36.6%), head/neck (37%), and trunk/extremities (26.4%).

    Related Experiment Videos

  • Diagnostic workup utilized instrumental methods, ultrasonography, and computed tomography.
  • Combined or complex treatment involving surgery, chemotherapy, and radiotherapy was employed, with two-year survival rates varying from 47% (head/neck) to 83% (orbit).

    • Impact:

    • Findings highlight the critical role of tumor site in determining prognosis for pediatric rhabdomyosarcoma.
    • The study underscores the need for tailored, multimodal treatment approaches.
    • Results contribute to understanding survival disparities and inform future research in pediatric soft tissue sarcomas.