Imaging of pediatric skull lytic lesions: A review

IF 2.3 4区 医学 Q3 CLINICAL NEUROLOGY
Mariana Santos, Bruno Cunha, Vasco Abreu, Suely Ferraciolli, Luís Godoy, Rodrigo Murakoshi, Lázaro Luís Faria Amaral, Carla Conceição
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引用次数: 0

Abstract

Skull lesions in pediatric population are common findings on imaging and sometimes with heterogeneous manifestations, constituting a diagnostic challenge. Some lesions can be misinterpreted for their aggressiveness, as with larger lesions eroding cortical bone, containing soft tissue components, leading to excessive and, in some cases, invasive inappropriate etiological investigation. In this review, we present multiple several conditions that may present as skull lesions or pseudolesions, organized by groups (anatomic variants, congenital and development disorders, traumatic injuries, vascular issues, infectious conditions, and tumoral processes). Anatomic variants are common imaging findings that must be recognized by the neuroradiologist. Congenital malformations are rare conditions, such as aplasia cutis congenita and sinus pericranii, usually seen at earlier ages, the majority of which are benign findings. In case of trauma, cephalohematoma, growing skull fractures, and posttraumatic lytic lesions should be considered. Osteomyelitis tends to be locally aggressive and may mimic malignancy, in which cases, the clinical history can be the key to diagnosis. Vascular (sickle cell disease) and tumoral (aneurismal bone cyst, eosinophilic granuloma, metastases) lesions are relatively rare lesions but should be considered in the differential diagnosis, in the presence of certain imaging findings. The main difficulty is the differentiation between the benign and malignant nature; therefore, the main objective of this pictorial essay is to review the main skull lytic lesions found in pediatric age, describing the main findings in different imaging modalities (CT and MRI), allowing the neuroradiologist greater confidence in establishing the differential diagnosis, through a systematic and simple characterization of the lesions.

儿童颅骨溶解性病变的影像学研究:综述。
儿童人群的颅骨病变是常见的影像学表现,有时表现为异质性,构成诊断挑战。一些病变可能因其侵袭性而被误解,因为较大的病变侵蚀皮质骨,含有软组织成分,导致过度的,在某些情况下,侵入性不适当的病因调查。在这篇综述中,我们提出了多种可能表现为颅骨病变或假性病变的疾病,按组组织(解剖变异、先天性和发育障碍、创伤、血管问题、感染性疾病和肿瘤过程)。解剖变异是常见的影像学发现,必须由神经放射科医生识别。先天性畸形是一种罕见的疾病,如先天性皮肤发育不全和颅周窦,通常在早期发现,其中大多数是良性的。在创伤的情况下,应考虑头部血肿、颅骨生长性骨折和创伤后溶解性病变。骨髓炎往往具有局部侵袭性,可能类似于恶性肿瘤,在这种情况下,临床病史可能是诊断的关键。血管性(镰状细胞病)和肿瘤性(动脉瘤性骨囊肿、嗜酸性肉芽肿、转移)病变是相对罕见的病变,但在有某些影像学表现的情况下,应在鉴别诊断中考虑。主要的困难是区分良性和恶性的性质;因此,这篇图片文章的主要目的是回顾在儿童年龄发现的主要颅骨溶解性病变,描述不同成像模式(CT和MRI)的主要发现,通过对病变的系统和简单表征,让神经放射科医生更有信心建立鉴别诊断。
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 Neuroimaging
Journal of Neuroimaging 医学-核医学
CiteScore
4.70
自引率
0.00%
发文量
117
审稿时长
6-12 weeks
期刊介绍: Start reading the Journal of Neuroimaging to learn the latest neurological imaging techniques. The peer-reviewed research is written in a practical clinical context, giving you the information you need on: MRI CT Carotid Ultrasound and TCD SPECT PET Endovascular Surgical Neuroradiology Functional MRI Xenon CT and other new and upcoming neuroscientific modalities.The Journal of Neuroimaging addresses the full spectrum of human nervous system disease, including stroke, neoplasia, degenerating and demyelinating disease, epilepsy, tumors, lesions, infectious disease, cerebral vascular arterial diseases, toxic-metabolic disease, psychoses, dementias, heredo-familial disease, and trauma.Offering original research, review articles, case reports, neuroimaging CPCs, and evaluations of instruments and technology relevant to the nervous system, the Journal of Neuroimaging focuses on useful clinical developments and applications, tested techniques and interpretations, patient care, diagnostics, and therapeutics. Start reading today!
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