Rhabdoid tumors (RT), or malignant rhabdoid tumors, are among the most aggressive and
lethal forms of human cancer. They can arise in any location in the body but are most …

Paediatric chordomas are rare malignant tumours arising from primitive notochordal
remnants with a high rate of recurrence. Only 5% of them occur in the first two decades such …

Soft tissue sarcomas are rare malignant heterogenous tumors of mesenchymal origin with
over fifty subtypes. The use of hematoxylin and eosin stained sections (and …

Purpose Atypical teratoid rhabdoid tumors (AT/RT) are rare, aggressive, central nervous
system neoplasms that typically affect children under 3 years of age and have a very poor …

Background: Chordoma is a rare primary malignant bone tumour. Treatment options are
mainly restricted to surgical excision, since chordomas are largely resistant to conventional …

Many benign and malignant soft tissue tumors in children are challenging and their
diagnosis requires knowledge of their vast diversity, histopathological complexity, and …