Wang Cheng-Sheng, Duan Qing, Xue Yun-Jing, Huang Xin-Ming, Wang Li-Li, Chen Zhi-Yong, Chen Jian-Hua, Sun Bin
Department of Radiology, Union Hospital, Fujian Medical University, No. 29, Xinquan Road, Fuzhou, 350001, China.
Radiol Med. 2015 Aug;120(8):745-52. doi: 10.1007/s11547-015-0520-6. Epub 2015 Feb 20.
The purpose of this study was to review the clinical and imaging characteristics of giant cell tumour of tendon sheath (GCTTS) with bone invasion.
Radiography (n = 9), magnetic resonance imaging (MRI) (n = 7), computed tomography (CT) (n = 4) and clinical findings of nine patients with surgically and pathologically confirmed GCTTS with bone invasion were retrospectively reviewed. Specific imaging findings including tumour site, maximum tumour size, shape, margin, density or signal intensity, bone invasion, periosteal reaction, calcification, and cystic areas were documented.
There were five males and four females, with median age of 34 years. Presenting symptoms were painless mass in five patients, painful mass in two, intermittent pain and swelling in one and pain without mass in one. Five tumours were in the ankle-foot region, two in the hand, one in the cubital fossa and one in the patellofemoral joint. The total symptom duration ranged from 5 months to 6 years (median 12 months). The maximum tumour size ranged from 1.0 to 6.8 cm (median 3.0 cm). Radiographically, all tumours appeared as cortical destruction with well-defined margins. Four patients underwent CT scanning that clearly showed an iso-attenuated mass with intraosseous soft tissue. MR scanning was performed in seven patients who demonstrated a round, oval, spindle-shaped or multilobular soft tissue mass near or inside the joint with cortical destruction and intraosseous soft tissue. Five lesions were homogeneous moderate signal on T1WI. Moderate (n = 1), slightly high or high (n = 2) and low (n = 2) signal intensities were evident on T2WI. Two lesions showed heterogeneous low-to-moderate signal intensities on T1WI and mixed low signal intensities on T2WI.
GCTTS is a benign soft tissue mass that may present as an intraosseous lesion near extremity joints and frequently occurring in foot and hand on radiological examinations. GCTTS with bone invasion should be considered when MRI shows solid mass with characteristic low signal on T2-weighted images.
本研究旨在回顾伴有骨侵犯的腱鞘巨细胞瘤(GCTTS)的临床及影像学特征。
回顾性分析9例经手术及病理证实的伴有骨侵犯的GCTTS患者的X线检查(n = 9)、磁共振成像(MRI)(n = 7)、计算机断层扫描(CT)(n = 4)及临床资料。记录肿瘤部位、最大肿瘤大小、形态、边界、密度或信号强度、骨侵犯、骨膜反应、钙化及囊性区域等具体影像学表现。
患者中男性5例,女性4例,中位年龄34岁。临床表现为5例患者为无痛性肿块,2例为疼痛性肿块,1例为间歇性疼痛伴肿胀,1例为无肿块的疼痛。5个肿瘤位于踝足部,2个位于手部,1个位于肘窝,1个位于髌股关节。症状持续时间总计5个月至6年(中位时间12个月)。最大肿瘤大小为1.0至6.8 cm(中位大小3.0 cm)。X线表现为所有肿瘤均呈边界清晰的皮质破坏。4例患者行CT扫描,清晰显示等密度肿块伴骨内软组织。7例患者行MR扫描,显示关节附近或关节内圆形、椭圆形、梭形或多叶状软组织肿块,伴皮质破坏及骨内软组织。5个病灶在T1WI上呈均匀中等信号。T2WI上可见中等信号(n = 1)、稍高或高信号(n = 2)及低信号(n = 2)。2个病灶在T1WI上呈不均匀低至中等信号,T2WI上呈混合低信号。
GCTTS是一种良性软组织肿块,可表现为四肢关节附近的骨内病变,影像学检查常见于足和手部。当MRI显示T2加权像上特征性低信号的实性肿块时,应考虑伴有骨侵犯的GCTTS。