A Case Report on Infantile Non-rhab Domyosarcoma in Foot: Therapeutic and Diagonistic Assay

Nonrhabdmyosarcoma soft tissue sarcomas (NRSTS) include a cluster of different types of soft tissue sarcomas clubbed together due to the rarity of individual subtypes. The diagnostic accuracy is lately reinforced due to the availability of immunohistochemical and molecular markers. So, there is still uncertain con-sensus for treatment protocol, however, neo- adjuvant chemotherapy modality was ultima- tely promising in our case. A healthy 3-month-old girl born with NSVD experiences and swelling on her right foot. The parents were consulted a pediatrician, who prescribes symptomatic treatment, and when the girl's pain worsens, they refer her to an orthopaedist. There, she was reexamined and diagnosed with an infantile malignant mesenchymal tumor after a series of MRIs and biopsies revealed mass.

After prospering neo-adjuvant treatment reduced mass was carefully excised within wide excision criteria and with safe surgical borders. Mass enfolded metatarsals then stripped off and fixed back after gamma irradiation. Although limb salvage surgery frequently prevents amputation, preserving the patient's life comes first before saving the patient's limb and functionality.