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颅底弥漫性腱鞘巨细胞瘤累及腱鞘的影像学表现。

Image findings of tendon sheaths affected by diffuse tenosynovial giant cell tumors of the skull base.

作者信息

Zhao S-S, Cheng J-L, Gao E-Y, Bai J, Zhang Y

机构信息

The First Affiliated Hospital of Zhengzhou University, Zhengzhou City, Henan Province, China.

出版信息

Eur Rev Med Pharmacol Sci. 2023 Mar;27(6):2571-2579. doi: 10.26355/eurrev_202303_31794.

DOI:10.26355/eurrev_202303_31794
PMID:37013775
Abstract

OBJECTIVE

This study investigated radiographic images and the differential diagnosis of intracranial diffuse tenosynovial giant cell tumor (D-TGCT) in order to better understand the disease and improve the rate of preoperative diagnosis.

PATIENTS AND METHODS

Images and clinical data of patients with D-TGCT were retrospectively analyzed. Routine Computer Tomography (CT), routine Magnetic Resonance Imaging (MRI), and contrast-enhanced MRI were performed for nine cases. Susceptibility-weighted imaging (SWI) was also performed for one case.

RESULTS

We reviewed nine patients (6 males and 3 females) aged between 24 and 64 years, with a mean age of 47.33 ± 14.92 years. The most frequent complaints were hearing loss (5/9, 55.6%), pain (4/9, 44%), masticatory symptoms (2/9, 22.2%), and mass (4/9, 44.4%), with a mean duration of 22 ± 21.43 months. All cases were centered on the base of the skull, and showed hyper-density soft-tissue mass with osteolytic bone destruction on CT. The tumor signal mainly showed iso-intensity or hypo-intensity on T1WI compared with that in the brain parenchyma in all patients. On T2WI, nine lesions mainly showed hypo-intensity. Among these nine lesions, three displayed cystic region showing hyper-intensity on T2WI and hypo-intensity on T1WI (Figure 2A, 2B) in the lesion. Nine lesions showed hypo-intensity on DWI sequences. SWI images presented low signal in two cases, showing the "flowering effect". Nine patients showed heterogeneous enhancement, and two patients had meningeal thickening.

CONCLUSIONS

Intracranial D-TGCT is extremely rare, but must be differentiated from other tumors. Osteolytic bone destruction in the area of the skull base with hyper-density soft-tissue mass and hypo-intensity on T2WI images are indicative of D-TGCT.

摘要

目的

本研究对颅内弥漫性腱鞘巨细胞瘤(D-TGCT)的影像学表现及鉴别诊断进行了研究,以更好地了解该疾病并提高术前诊断率。

患者与方法

回顾性分析D-TGCT患者的影像学资料和临床数据。对9例患者进行了常规计算机断层扫描(CT)、常规磁共振成像(MRI)及增强MRI检查,对1例患者进行了磁敏感加权成像(SWI)检查。

结果

我们共纳入9例患者(6例男性,3例女性),年龄在24至64岁之间,平均年龄为47.33±14.92岁。最常见的症状为听力下降(5/9,55.6%)、疼痛(4/9,44%)、咀嚼症状(2/9,22.2%)和肿块(4/9,44.4%),平均病程为22±21.43个月。所有病例均以颅底为中心,CT表现为高密度软组织肿块伴骨质溶解破坏。所有患者肿瘤在T1WI上与脑实质相比主要呈等信号或低信号。在T2WI上,9个病灶主要呈低信号。其中9个病灶中有3个在病灶内显示T2WI呈高信号、T1WI呈低信号的囊性区域(图2A、2B)。9个病灶在扩散加权成像(DWI)序列上呈低信号。SWI图像在2例中呈低信号,表现为“开花效应”。9例患者均表现为不均匀强化,2例患者有脑膜增厚。

结论

颅内D-TGCT极为罕见,但必须与其他肿瘤相鉴别。颅底区域骨质溶解破坏伴高密度软组织肿块及T2WI图像上呈低信号提示D-TGCT。

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