Abstract
Abstract Congenital infantile sarcoma is a rare tumor. Any part of the body can be affected, but upper and lower extremities are common sites of the disease. Diagnosis is reached by clinical presentation, radiological findings, immunohistochemical evaluation and molecular detection of chromosomal abnormality associated with the disease. Differential diagnosis depends on tumor location. Surgical excision is the treatment of choice. Chemotherapy can be of value when complete surgical resection is not possible. Radiotherapy role is limited and needs further evaluation. Here we present a case of huge congenital infantile sarcoma. To the best of our knowledge, this is the first case in literature reporting congenital infantile sarcoma arising from the abdominal wall.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: 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.