Sarcoma epitelioide

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Norton Children’s Cancer Institute

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Epithelioid sarcoma is a rare soft tissue cancer that typically appears in teens and young adults. Firm, painless lumps start to appear under the skin of extremities such as the fingers, hands, feet, forearms and lower legs. Sometimes the lumps develop into open sores.

Epithelioid sarcoma tends to affect males more than females, and females with the cancer tend to have a less aggressive form. Smaller tumors (less than ¾ inch in diameter) and lesions on the hands or feet that appear at an early age also tend to have better success with treatment.

Early diagnosis and treatment of epithelioid sarcoma improves the chance of long-term survival. Because the disease can appear as a benign (noncancerous) condition in its early stages, it’s crucial to get a diagnosis from a pediatric specialist with extensive experience.

The board-certified and fellowship-trained oncologists at Norton Children’s Cancer Institute, affiliated with the UofL School of Medicine, come together at regular conferences to share viewpoints from various perspectives that help determine the best course of treatment. It’s like getting second, third and fourth opinions all at once.

Our physicians actively conduct clinical trials and publish their discoveries about new ways to identify and treat sarcomas and other pediatric cancers.

By staying at the forefront of research, our physicians are experienced with newly approved therapies and can provide access to trials of experimental treatments.

Diagnosis and Treatment of Epithelioid Sarcoma

Diagnosis of epithelioid sarcoma requires skill and experience, as patients with this type of cancer typically have a mass or swelling as their only symptom. The tumor may appear to be nothing more than a common skin infection.

Examination at a comprehensive pediatric cancer center like Norton Children’s Cancer Institute means the patient is seen by specialists with experience diagnosing and treating epithelioid sarcoma. Our specialists are leaders in advancing knowledge of the disease.

MRI is a common test to determine the type and size of the mass. A small sample of tissue from the mass will be removed (biopsied) for examination by a pathologist to determine whether it is cancer.

Surgery can cure epithelioid sarcoma in cases where the cancer hasn’t spread to the lymph nodes, lungs or other locations. Surgery will involve removing the diseased tissue and some healthy tissue to reduce the risk of recurrence. In some cases, amputation may be necessary.

Radiation therapy may be used before surgery to shrink the tumor and after surgery to reduce the chance of recurrence.

Epithelioid sarcoma has the best chance of being cured when it’s treated by pediatric cancer specialists. Young adults may benefit from treatment at a children’s hospital instead of an adult-service hospital because the care team has expertise specifically in childhood diseases.

La diferencia de Norton Children’s

El programa de atención oncológica del Norton Children’s Hospital es uno de los programas de oncología más antiguos de EE. UU. con acreditación constante del Comité del Cáncer del Colegio Americano de Cirujanos. Con el respaldo de casi 60 años de experiencia en pediatría, contamos con un equipo de atención oncológica con experiencia compuesto por más de 200 especialistas líderes en cáncer, que incluye oncólogos, cirujanos, enfermeros, trabajadores sociales, capellanes, conductistas, terapeutas y farmacéuticos. Este equipo multidisciplinario capacitado se concentra por completo en las necesidades de su hijo y su familia.

Además, contamos con:

  • El principal programa multidisciplinario de tumores cerebrales pediátricos de Kentucky
  • Los únicos programas de aféresis pediátrica y fotoféresis pediátrica de Kentucky
  • Un programa de inmunoterapia
  • Uno de los programas de tratamiento de la anemia falciforme más grandes del país
  • La principal clínica de transición y programa para adolescentes y adultos jóvenes
  • El único tratamiento de terapia de células T con receptor de antígeno quimérico (T-RAQ) de Kentucky para pacientes pediátricos
  • Programa de supervivencia después del cáncer
  • Programa de hemorragia y coagulación pediátricas (hemostasia y trombosis)

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