J Korean Assoc Oral Maxillofac Surg.  2004 Jun;30(3):223-227.

A case report of Synovial sarcoma

Affiliations
  • 1Department of Oral and Maxillofacial Surgery, Dental College, Kyung-Hee University. leebs@khu.ac.kr
  • 2Department of Internal Medicine, Medical College, Kyung-Hee University.

Abstract

A malignant sarcoma of soft tissue that arises near but not in a joint, most often in an adolescent or young adult, is typically slowgrowing, and may escapes notice until it causes pain. The diagnosis of this tumor can be suspected by X-ray or imaging, made by biopsy, and confirmed by chromosome studies. Cytogenic studies reveal a translocation between the X chromosome and chromosome 18 in the tumor cells. The most common treatment for the tumor is surgery to remove the entire tumor, nearby muscle, and lymph nodes. Synovial sarcoma tends to recur locally and to involve regional lymph nodes. Distant metastasis occurs in half cases. The well-documented and adequately followed cases are currently lacking and this report described an instance of Synovial sarcoma good result after treatment and review of literature.

Keyword

Synovial sarcoma; Reconstruction with radial forearm flap; Recurrence

MeSH Terms

Adolescent
Biopsy
Chromosomes, Human, Pair 18
Diagnosis
Humans
Joints
Lymph Nodes
Neoplasm Metastasis
Recurrence
Sarcoma
Sarcoma, Synovial*
United Nations
X Chromosome
Young Adult
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