Fibromatosis Colli: A Thorough Description of Its MRI Characteristics and a Review of the Literature.

IF 1 4区 医学 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Journal of the Belgian Society of Radiology Pub Date : 2024-05-07 eCollection Date: 2024-01-01 DOI:10.5334/jbsr.3270
Thomas Saliba, Marco Preziosi, Paolo Simoni, Alessandro De Leucio
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引用次数: 0

Abstract

Introduction: Fibromatosis colli (FC) is a rare pseudotumor of the sternocleidomastoid muscle with an incidence of 0.4%, generally diagnosed using ultrasound between 2 and 4 weeks of age. This is an important entity considering the clinical concerns it causes due to its appearance as a cervical mass with torticollis. Few magnetic resonance imaging (MRI) descriptions of its appearance have been made, with the existing reported cases being sporadic. We aim to provide a thorough description of this paediatric entity.

Materials and methods: We conducted a retrospective study by searching our hospital's database for previous cases of FC where an MRI had been performed. We found six cases of FC where an MRI had been performed. Of these cases, five out of six were contrast-enhanced. We examined the MRIs to be able to discern and describe the MRI characteristics of FC.

Results: We found that FC presents a T1 signal isointense to the muscle, a T2 signal hyperintense to the muscle, a variable diffusion signal and a thick enhancing peripheral ring after contrast administration.

Discussion: Our results match what has been reported in the literature to date regarding the MRI signal of FC, confirming previous reports. However, we provide new data regarding the characteristic appearance post-enhancement, which was previously unreported.

Conclusion: The MRI characteristics of FC have rarely been described, with only a few isolated case reports in the medical literature. We review the current literature, describe the key MRI characteristics of the pathology, and provide the most thorough description to date.

胶状纤维瘤病:磁共振成像特征的详尽描述和文献综述。
简介胸锁乳突肌纤维瘤病(Fibromatosis colli,FC)是一种罕见的胸锁乳突肌假瘤,发病率为 0.4%,一般在婴儿 2 到 4 周大时通过超声波检查确诊。考虑到其临床表现为颈部肿块并伴有迂曲性颈椎病,因此是一种重要的疾病。磁共振成像(MRI)对其外观的描述很少,现有报道的病例均为散发性。我们的目的是对这种儿科疾病进行全面的描述:我们进行了一项回顾性研究,在本医院的数据库中搜索了以前进行过核磁共振成像的 FC 病例。我们发现有六例 FC 病例曾进行过核磁共振成像检查。在这些病例中,六例中有五例为对比增强型。我们对核磁共振成像进行了检查,以辨别和描述 FC 的核磁共振成像特征:结果:我们发现,FC 的 T1 信号与肌肉呈等密度,T2 信号与肌肉呈高密度,弥散信号可变,使用造影剂后,外周呈厚增强环:我们的研究结果与迄今为止有关 FC MRI 信号的文献报道一致,证实了之前的报道。讨论:我们的结果与迄今为止有关 FC MRI 信号的文献报道一致,证实了之前的报道,但我们提供了有关增强后特征性外观的新数据,而这在之前是没有报道过的:结论:FC 的 MRI 特征很少被描述,医学文献中仅有个别病例报道。我们回顾了当前的文献,描述了该病变的主要 MRI 特征,并提供了迄今为止最详尽的描述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of the Belgian Society of Radiology
Journal of the Belgian Society of Radiology Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
0.70
自引率
5.00%
发文量
96
期刊介绍: The purpose of the Journal of the Belgian Society of Radiology is the publication of articles dealing with diagnostic and interventional radiology, related imaging techniques, allied sciences, and continuing education.
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