Introduction: Rhabdomyosarcoma is the most frequently occurring intrusive soft tissue sarcoma in the pediatric age group. Orbit is the most common location for a pediatric rhabdomyosarcoma, but it can occur in the oral cavity, pharynx, face and neck in the descending order of incidence. Rhabdomyosarcoma in the ear is extremely rare.   Case Report: A 5-year-old girl prese...

rhabdomyosarcoma is a common primary childhood malignancy that rarely metastasizes to the breast. we report a patient with a primary sinonasal rhabdomyosarcoma metastasizing to the breast, with no distant spread. we describe the imaging appearance of rhabdomyosarcoma on magnetic resonance imaging (mri), particularly on diffusion-weighted imaging (dwi) and apparent diffusion coefficient (adc) se...

Paratesticular Rhabdomyosarcoma is a rare mesenchymal tumor. The Alveolar variant the one with worse prognosis. It comprehend 20% of cases. treatment multimodal combining surgery, chemotherapy and radiotherapy. Depending on extent disease staging group, approach different. Here we report case an alveolar rhabdomyosarcoma review literature regarding this unusual clinical entity.

Introduction Presence of two primary malignancies is rare and occurs in 3-5% of the cancer patients. As per our extensive internet research, this is the only reported case of a synchronous sino-nasal embryonal rhabdomyosarcoma with squamous cell carcinoma-tongue. The case report is important because of the rare diagnosis and the challenge we faced in the diagnosis and treatment of the pat...

Congenital or neonatal rhabdomyosarcoma is a rare entity, usually presenting as masses in the head and neck region as well as genitourinary tract. The embryonal variant is the most common type occurring in infancy. This is a case of congenital rhabdomyosarcoma with a huge forearm mass, with metastatic discrete nodules in the soft tissues of the neck and scapular region, resembling a ‘blueberry ...

We report 5 cases of sclerosing rhabdomyosarcoma. The patients included 4 adults and 1 adolescent. In the 5 cases, 3 tumors occurred in the head and neck region and 2 in an extremity. Histologically, all 5 tumors were characterized by the presence of abundant extracellular hyaline matrix, mimicking osteoid or chondroid tissue. They were composed mostly of primitive small round cells that displa...

Rhabdomyosarcoma, which accounts for 20% of all malignant tumors the heart, is an aggressive tumor originating in ventricular wall. These are second most common primary heart after angiosarcoma. Despite treatment options, such as surgical resection, radiotherapy, and chemotherapy, recurrence mortality high. Among these patients, survival with resection around six months to one year. In this cas...

Abstract Background: Rhabdomyosarcoma is the most common soft tissue sarcoma among children which has two major subtypes: embryonal rhabdomyosarcoma (ERMS) and alveolar rhabdomyosarcoma (ARMS). Distinction between these subtypes is mandatory to choose proper treatment and to determine prognosis. Histopathologic study is the main method, but nowadays molecular studies like PCR are also used...