Korean J Dermatol.  2008 Oct;46(10):1427-1431.

Primary Cutaneous Extraskeletal Ewing's Sarcoma

Affiliations
  • 1Department of Dermatology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. miumiu@amc.seoul.kr

Abstract

Extraskeletal Ewing's sarcoma has been recognized as being histologically indistinguishable from Ewing's sarcoma of bone. Histopathologically, Ewing's sarcoma consists of solid sheets of small round cells with vesicular nuclei and scant cytoplasm, and the cells are arranged in irregular masses separated by strands of fibrous tissue. Extraskeletal Ewing's sarcoma may arise virtually anywhere, but it is most common in the deep soft tissues of the extremities. We report here on a 27-year-old woman with cutaneous extraskeletal Ewing's sarcoma. She presented with a subcutaneous tumor of the right upper arm, and this was without osseous involvement. The patient underwent wide local excision and she received chemotherapy with vincristine, cyclophosphamide, etoposide and ifosfamide. There has been no evidence of recurrence or metastasis during 16 months of follow up.

Keyword

Extraskeletal Ewing's sarcoma; Skin

MeSH Terms

Adult
Arm
Cyclophosphamide
Cytoplasm
Etoposide
Extremities
Female
Follow-Up Studies
Humans
Ifosfamide
Neoplasm Metastasis
Recurrence
Sarcoma, Ewing
Skin
Vincristine
Cyclophosphamide
Etoposide
Ifosfamide
Vincristine
Full Text Links
  • KJD
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr