| Literature DB >> 17197895 |
Akira Mitsuhashi1, Yuichiro Nagai, Kiyomi Suzuka, Koji Yamazawa, Takayuki Nojima, Takashi Nikaido, Hiroshi Ishikura, Hideo Matsui, Makio Shozu.
Abstract
Synovial sarcoma, a malignant mesenchymal neoplasm, occurs mostly near the joints of the extremities and occasionally outside the joint such as lung. We report a case of soft tissue sarcoma arising in the fallopian tube origin that showed characteristic pathological appearance of biphasic synovial sarcoma. Molecular analysis detected a fusion gene transcript of synovial sarcoma translocation (SYT) gene from chromosome 18 and synovial sarcoma X chromosome breakpoint 1 (SSX1) gene, which is believed to pathognomonic for synovial sarcoma of joint origin. Recurrent abdominal tumor, observed at 12 month after the initial surgery and following chemotherapy using doxorubicin, cisplatin and ifosfamide, partially responded to chemotherapy using paclitaxel and carboplatin and, then, optimal surgery was performed. This is the first report of a synovial sarcoma arising in the fallopian tube.Entities:
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Year: 2007 PMID: 17197895 DOI: 10.1097/01.pgp.0000225841.13880.3a
Source DB: PubMed Journal: Int J Gynecol Pathol ISSN: 0277-1691 Impact factor: 2.762