Mitsuhashi Akira, Nagai Yuichiro, Suzuka Kiyomi, Yamazawa Koji, Nojima Takayuki, Nikaido Takashi, Ishikura Hiroshi, Matsui Hideo, Shozu Makio
Department of Reproductive Medicine, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba 260-8670, Japan.
Int J Gynecol Pathol. 2007 Jan;26(1):34-7. doi: 10.1097/01.pgp.0000225841.13880.3a.
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.
滑膜肉瘤是一种恶性间叶性肿瘤,大多发生于四肢关节附近,偶尔也发生于关节外,如肺部。我们报告一例起源于输卵管的软组织肉瘤病例,其表现出双相滑膜肉瘤的特征性病理外观。分子分析检测到18号染色体上的滑膜肉瘤易位(SYT)基因与滑膜肉瘤X染色体断点1(SSX1)基因的融合基因转录本,这被认为是关节起源滑膜肉瘤的特征性表现。在初次手术及使用阿霉素、顺铂和异环磷酰胺化疗12个月后观察到复发性腹部肿瘤,其对使用紫杉醇和卡铂的化疗部分有反应,随后进行了最佳手术。这是首例关于起源于输卵管的滑膜肉瘤的报告。