Department of Radiology, Children's Hospital of Philadelphia, 3401 Civic Center Blvd., Philadelphia, PA, 19104, USA.
University of Pennsylvania School of Medicine, Philadelphia, PA, USA.
Pediatr Radiol. 2021 Mar;51(3):441-449. doi: 10.1007/s00247-020-04861-4. Epub 2020 Nov 6.
Magnetic resonance imaging (MRI) plays a critical role in disease characterization of intra-articular tenosynovial giant cell tumor.
To characterize the MRI features of intra-articular tenosynovial giant cell tumor in children with respect to disease subtype and anatomical location.
This retrospective study included children with tenosynovial giant cell tumor who underwent preoperative MRI between January 2006 and May 2020. Two radiologists reviewed each examination to determine disease subtype, signal intensities and the presence of an effusion, osseous changes, chondromalacia, juxtacapsular disease and concomitant joint involvement. Fisher exact, Mann-Whitney U, and Kruskal-Wallis H tests were used to compare findings between subtypes and locations.
Twenty-four children (16 girls, 8 boys; mean age: 13.1±3.8 years) with 19 knee and 5 ankle-hindfoot tenosynovial giant cell tumor had either diffuse (n=15) or localized (n=9) disease. An effusion (P=0.004) was significantly more common with diffuse than localized disease. There was no significant difference in MRI signal (P-range: 0.09-1) or other imaging findings (P-range: 0.12-0.67) between subtypes. Children with knee involvement were significantly more likely to present with diffuse disease while those with ankle-hindfoot involvement all presented with focal disease (P=0.004). Juxtacapsular (n=4) and concomitant proximal tibiofibular joint involvement (n=5) were observed with diffuse disease in the knee. Erosions (P=0.01) were significantly more common in the ankle than in the knee.
In our study, diffuse tenosynovial giant cell tumor was more common than localized disease, particularly in the knee where juxtacapsular and concomitant proximal tibiofibular joint disease can occur.
磁共振成像(MRI)在关节内腱鞘巨细胞瘤的疾病特征中起着关键作用。
描述儿童关节内腱鞘巨细胞瘤的 MRI 特征,包括疾病亚型和解剖部位。
本回顾性研究纳入了 2006 年 1 月至 2020 年 5 月间接受术前 MRI 检查的腱鞘巨细胞瘤患儿。两名放射科医生对每一次检查进行评估,以确定疾病亚型、信号强度以及是否存在积液、骨改变、软骨软化、关节囊旁病变和关节受累。采用 Fisher 确切概率检验、Mann-Whitney U 检验和 Kruskal-Wallis H 检验比较各亚型和部位间的发现。
24 例患儿(16 名女孩,8 名男孩;平均年龄 13.1±3.8 岁)中,19 例为膝关节,5 例为踝关节-后足腱鞘巨细胞瘤,分别表现为弥漫型(n=15)或局限型(n=9)病变。弥漫型较局限型更常出现积液(P=0.004)。MRI 信号(P 值范围:0.09-1)或其他影像学表现(P 值范围:0.12-0.67)在各亚型间无显著差异。膝关节受累患儿更常表现为弥漫型,而踝关节-后足受累患儿均表现为局限型(P=0.004)。膝关节弥漫型可见关节囊旁(n=4)和胫腓骨近端关节同时受累(n=5)。踝关节较膝关节更常出现侵蚀(P=0.01)。
在我们的研究中,弥漫型腱鞘巨细胞瘤比局限型更常见,特别是在膝关节,可能发生关节囊旁和胫腓骨近端关节同时受累。