Background Rhabdomyosarcoma (RMS), a common soft-tissue malignancy in pediatrics,
presents high invasiveness and mortality. However, besides known changes in the PAX3/7 …

Background: Alveolar rhabdomyosarcoma (ARMS) shows a predilection for the peripheral
extremities and is very rarely identified as a primary in the brain. Here, we report a case of …

Objectives Epithelioid rhabdomyosarcoma (EpiRMS) is a novel morphologically distinct
variant of rhabdomyosarcoma, with an unusually challenging microscopic diagnosis. The …

Background Teratoma with nephroblastoma (TWN) is an extremely rare condition. Since
1984, only 45 reported cases have been identified. To our knowledge, there have been only …

Background Rhabdomyosarcoma (RMS) is a rare malignant soft tissue sarcoma with a poor
outcome and unclear prognostic factors. The purpose of this study was to analyze the …

Rhabdomyosarcoma is a malignant tumor of striated muscle tissue that can exceptionally
present in the pleura. Its prognosis is generally poor. We report a case of an eight-year-old …

Primitive neuroectodermal tumor (PNET) belongs to the class of malignant round cell tumor.
PNETs show varying degree of neuroectodermal differentiation. They are one of the most …

Rhabdomyosarcoma (RMS) is a rare, rapidly growing, highly aggressive malignant
neoplasm, originating from undifferentiated mesenchymal cells that retain their ability to …

Rhabdomyosarcoma (RMS) is a highly aggressive lesion and is commonly seen in children
below the age of 10 years. The survival rate is not very high as an early diagnosis is often …

Rhabdomyosarcoma (RMS) is the most prevalent pediatric soft tissue malignancy. The early
metastasis and recurrence of RMS, as well as the pain and bleeding induced by tumor …