首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >Parry Romberg syndrome: Imaging features in 4 consecutive cases and review of literature
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Parry Romberg syndrome: Imaging features in 4 consecutive cases and review of literature

机译:Parry Romberg综合症:连续4个案例中的成像功能和文学审查

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摘要

Parry Romberg syndrome (PRS) is a distinct sporadic self-limiting entity comprising progressive hemiatrophy of the face with predisposition to affect the skin, subcutaneous tissue and in some cases deeper extension to the cartilage, osseous structures and musculature (Wong et al., 2015; Aydin et al., 2015; Sharma et al., 2012) [1-3]. Neurologic and ocular involvement is variable as is the progression of this entity. With a multitude of aetiologies ranging from autoimmune to infectious this syndrome is a diagnosis of exclusion, with a highly variable prognosis, drawing the amusement of radiologists and clinicians. Radiological assessment and subsequent diagnosis of this entity can aid in alleviating the lifestyle hampering progression of this disease process. We hereby report 4 cases of this syndrome and aim to describe the varied radiological presentations of this entity with concise review of literature. (C) 2020 Elsevier Ltd. All rights reserved.
机译:Parry Romberg综合征(PRS)是一种不同的散发性自我限制实体,包括面部的渐进性血管性,具有倾向于影响皮肤,皮下组织,以及在某些情况下更深入地延伸到软骨,骨质结构和肌肉组织(Wong等,2015年 ; Aydin等,2015; Sharma等,2012)[1-3]。 神经系统和眼镜参与是可变的,也是该实体的进展。 对于感染自身免疫性的众多的疾病来说,这种综合征是排除的诊断,具有高度可变的预后,吸引放射科和临床医生的娱乐。 放射性评估和随后对该实体的诊断可以帮助缓解妨碍这种疾病过程的生活方式。 我们在此报告了4例本综合征,并旨在描述本实体的各种放射性介绍,并简明地审查文献。 (c)2020 elestvier有限公司保留所有权利。

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