Key result
A case report of a 7-year-old girl from Bangladesh describes the clinical, radiological, and histological features of oral embryonal rhabdomyosarcoma.
Case Report (n=1)
No
This case report details the presentation and diagnosis of oral embryonal rhabdomyosarcoma in a pediatric patient.
May aid recognition of rare pediatric oral tumors; extends limited case literature without informing practice.
Rhabdomyosarcoma is a malignant skeletal muscle neoplasm which frequently involves head and neck region. It is the second most common soft tissue sarcoma encountered in children. RMS is an aggressive neoplasm with extensive local invasions and early hemorrhagic and lymphatic dissemination. Here, we report a case of oral RMS in a 7-year-old girl from Bangladesh. Histologically, the tumor consisted of a classic embrayonal rabdosarcomatous area was observed in the biopsy specimen. Furthermore, we discuss about the clinical, radiological, immunohistochemical findings, and management of the aforementioned RMS case.
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Sadat et al. (2020) conducted a case report in Oral rhabdomyosarcoma (n=1). Oral rhabdomyosarcoma was evaluated on Clinical, radiological, immunohistochemical findings, and management. A case report of a 7-year-old girl from Bangladesh describes the clinical, radiological, and histological features of oral embryonal rhabdomyosarcoma.
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