Epithelioid sarcoma is a mesenchymal soft tissue sarcoma often arising in the extremities,
usually in young adults with a pick of incidence at 35 years of age. Epithelioid sarcoma (ES) …

Epithelioid sarcoma (ES) is a very rare and aggressive mesenchymal tumor of unclear origin
and uncertain lineage characterized by a prevalent epithelioid morphology. The only …

Epithelioid sarcoma (ES) is a soft tissue sarcoma of children and young adults for which the
preferred treatment for localized disease is wide surgical resection. Medical management is …

Soft tissue sarcomas are an uncommon and diverse group of more than 50 mesenchymal
malignancies. The pathogenesis of many of these is poorly understood, but others have …

Introduction Epithelioid sarcoma (ES) is a rare soft tissue sarcoma subtype, predominantly
occurring in children and young adults. Despite optimal management of localized disease …

Purpose: Molecular deregulations underlying epithelioid sarcoma (ES) progression are
poorly understood yet critically needed to develop new therapies. Epidermal growth factor …

Simple Summary Near-infrared imaging of tumors during surgery facilitates the oncologic
surgeon to distinguish malignant from healthy tissue. The technique is based on fluorescent …

Background Epithelioid sarcomas and rhabdoid tumors are rare, aggressive malignancies
with poor prognosis. Both are characterized by INI1 alterations and deregulation of growth …

Epithelioid sarcoma (ES) is a rare soft tissue neoplasm with high recurrence rates. Wide
surgical resection remains the only potential curative treatment. ES presents most commonly …

Epithelioid sarcoma (ES) is an aggressive malignant soft-tissue tumour which was first
named in the 1970s by Franz Enzinger (Enzinger, 1970). ES is rare, accounting for less than …