Nakanishi Hirofumi, Araki Nobuhito, Sawai Yuka, Kudawara Ikuo, Mano Masayuki, Ishiguro Shingo, Ueda Takafumi, Yoshikawa Hideki
Department of Orthopedic Surgery, Osaka Medical Center for Cancer and Cardiovascular Diseases, 1-3-3, Nakamichi, Higashinari-Ku, 537-8511 Osaka, Japan.
Skeletal Radiol. 2003 Dec;32(12):701-7. doi: 10.1007/s00256-003-0690-5. Epub 2003 Oct 15.
To characterize the radiological and clinicopathologic features of cystic synovial sarcoma.
Seven patients with primary cystic synovial sarcoma were evaluated. Computed tomography (CT) and magnetic resonance (MR) imaging were undertaken at the first presentation. The diagnosis of synovial sarcoma was made on the basis of histological examinations followed by molecular analysis. Radiological and clinicopathologic findings were reviewed.
CT showed well-defined soft tissue mass without cortical bone erosion and invasion. Calcification was seen at the periphery of the mass in three cases. T2-weighted MR images showed multilocular inhomogeneous intensity mass in all cases, five of which showed fluid-fluid levels. On gross appearance, old and/or fresh hematomas were detected in six cases. In the one remaining case, microscopic hemorrhage in the cystic lumen was proven. Four cases had poorly differentiated areas. In five cases prominent hemangiopericytomatous vasculature was observed. Histologic grade was intermediate in one tumor and high in six. One case had a history of misdiagnosis for tarsal tunnel syndrome, one for lymphadenopathy, two for sciatica and two for hematoma.
All cystic synovial sarcomas demonstrated multilocularity with well-circumscribed walls and internal septae. Synovial sarcoma should be taken into consideration in patients with deeply situated multicystic mass with triple signal intensity on T2-weighted MR imaging.
描述囊性滑膜肉瘤的放射学及临床病理特征。
对7例原发性囊性滑膜肉瘤患者进行评估。初次就诊时行计算机断层扫描(CT)及磁共振成像(MR)检查。滑膜肉瘤的诊断基于组织学检查并结合分子分析。回顾放射学及临床病理检查结果。
CT显示边界清晰的软组织肿块,无皮质骨侵蚀及侵犯。3例肿块周边可见钙化。T2加权MR图像显示所有病例均为多房性不均匀强化肿块,其中5例可见液-液平面。大体检查发现6例有陈旧性和/或新鲜血肿。其余1例经证实为囊腔内镜下出血。4例有低分化区域。5例可见显著的血管外皮细胞瘤样血管。1例肿瘤组织学分级为中级,6例为高级。1例曾被误诊为跗管综合征,1例误诊为淋巴结病,2例误诊为坐骨神经痛,2例误诊为血肿。
所有囊性滑膜肉瘤均表现为多房性,壁边界清晰,内部有分隔。对于T2加权MR成像显示为深部多房性肿块且具有三重信号强度的患者,应考虑滑膜肉瘤的可能。