Abstract
Rhabdomyosarcoma is a malignant mesenchymal tumor with skeletal muscle differentiation. It is the most common soft tissue sarcoma in children and adolescents. Its incidence is 4.5 cases per 1 million people aged 0-20 year. Embryonal, alveolar, pleomorphic and sclerosing /spindle cell types are the major variants of rhabdomyosarcoma. Embryonal rhabdomyosarcoma is the most common type. Rhabdomyosarcoma is highly aggressive and usually patient presented with pressure symptoms or metastasis. We are reporting 2 cases of rhabdomyosarcoma with one patient presented with abdominal wall nodules and other patient with bilateral breast lumps.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
