Abdominal embryonal rhabdomyosarcoma. A case report.

H. Y. Huang*, H. C. Chang, C. H. Lai, Y. K. Soong, S. Hsueh

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

Abstract

Rhabdomyosarcoma is the most common soft tissue sarcoma in childhood, but it is rare in young adults. It usually occurs in the pelvis or genito-urinary tract. We report a case of abdominal embryonal rhabdomyosarcoma who received a combined treatment modality with radical pelvic surgery and combination chemotherapy of vincristine, actinomycin-D and cyclophosphamide (VAC). She is well with no evidence of tumour recurrence for 3 years after primary surgery.

Original languageEnglish
Pages (from-to)95-99
Number of pages5
JournalChang Gung Medical Journal
Volume15
Issue number2
StatePublished - 06 1992
Externally publishedYes

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