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伴局限性硬皮病的帕里-龙贝格综合征

Parry-Romberg Syndrome Associated with Localized Scleroderma.

作者信息

Maletic Jelena, Tsirka Vassiliki, Ioannides Panos, Karacostas Dimitrios, Taskos Nikolaos

机构信息

B Department of Neurology, AHEPA University Hospital, Thessaloniki, Greece.

出版信息

Case Rep Neurol. 2010 Jun 1;2(2):57-62. doi: 10.1159/000314927.

Abstract

Parry-Romberg syndrome is a rare neurocutaneous disorder of unknown origin. It is characterized by progressive facial hemiatrophy and frequently overlaps with a condition known as linear scleroderma 'en coup de sabre'. Neurological involvement is frequently described in these patients, including migraine, facial pain and epilepsy, which represent the commonest neurological conditions, sometimes associated with brain abnormalities ipsilaterally to the skin lesions. We present a case of Parry-Romberg syndrome with neurological involvement in a patient with diagnosed localized scleroderma (morphea).

摘要

帕里-龙贝格综合征是一种病因不明的罕见神经皮肤疾病。其特征为进行性面部半侧萎缩,常与一种称为“剑伤样”线状硬皮病的病症重叠。这些患者常出现神经受累情况,包括偏头痛、面部疼痛和癫痫,这些是最常见的神经病症,有时与皮肤病变同侧的脑部异常有关。我们报告一例已诊断为局限性硬皮病(硬斑病)且伴有神经受累的帕里-龙贝格综合征患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8659/2905582/7cc44f8abf00/crn0002-0057-f01.jpg

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