Idiopathic Harlequin syndrome.

Q4 Medicine
V. Voitenkov, V. Komantsev, E. Ekusheva, V. Y. Romanenko, M. A. Irikova
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引用次数: 0

Abstract

Harlequin syndrome (HA) is a rare pathology. It is manifested by isolated unilateral facial flushing (less often the face and limb), sometimes with concomitant hyperhidrosis and Horner’s syndrome. In most cases, this is an idiopathic condition with a benign course. However, HA can be a manifestation of serious diseases, as well as a complication of surgical interventions at the cervical and upper thoracic levels. We present clinical case of a female patient with Harlequin syndrome as well as a short review of scientific literature.
特发性哈勒金综合征
哈勒金综合征(HA)是一种罕见病。它表现为孤立的单侧面部潮红(面部和四肢较少见),有时伴有多汗症和霍纳综合征。在大多数情况下,这是一种特发性疾病,病程为良性。不过,HA 也可能是严重疾病的一种表现形式,也可能是颈椎和上胸椎手术治疗的并发症。我们将介绍一名女性哈勒金综合征患者的临床病例,并对科学文献进行简要回顾。
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
Russian Neurological Journal
Russian Neurological Journal Medicine-Neurology (clinical)
CiteScore
0.40
自引率
0.00%
发文量
49
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