Oculomotor nerve palsy, an unusual onset of polyarteritis nodosa.

IF 1.4 Q3 RHEUMATOLOGY
Reumatologia Pub Date : 2023-01-01 DOI:10.5114/reum/161085
Ana Martins, Filipe Oliveira Pinheiro, Sofia Vedor, Daniela Oliveira, Maria Seabra Rato, Diogo Fonseca, Pedro Madureira, Luís Braz, Sofia Pimenta, Lúcia Costa
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引用次数: 0

Abstract

Introduction: Cranial nerve involvement in polyarteritis nodosa(PAN) is underrecognized and rarely reported. The aim of this article is to review the available literature and present an example of oculomotor nerve palsy in the course of PAN.

Material and methods: Evaluation of texts describing the analyzed problem using the terms "polyarteritis nodosa", "nerve", "oculomotor", "cranial nerve" and "cranial neuropathy" for searching the PubMed database was done. Only full-text articles in English language with titles and abstracts were included in the analysis. As a guideline for the analysis of articles, the methodology described in the Principles of Individual Patient Data systematic reviews (PRISMA-IPD) was used.

Results: After screening articles only 16 reported cases of PAN with cranial neuropathy were included in the analysis. In 10 the cranial neuropathy was reported as the initial manifestation of PAN with optic nerve involvement as the most frequent (62.5%); among these cases the oculomotor nerve was involved in 3 cases. Treatment with glucocorticosteroids and cyclophosphamide was the most common.

Conclusions: Although cranial neuropathy, especially oculomotor nerve palsy is a rare first neurological manifestation of PAN, this clinical problem should be considered in the differential diagnosis.Especially patients with peripheral neuropathy, general symptoms, skin lesions and hepatitis B virus infection should be evaluated for cranial nerve involvement in the course of vasculitis.In the case of unclear involvement of the cranial nerves, PAN should also be considered in the differential diagnosis as the cause of symptoms and the first manifestation of the disease.

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动眼神经麻痹,一种不寻常的结节性多动脉炎。
颅神经受累于结节性多动脉炎(PAN)被低估且很少报道。本文的目的是回顾现有的文献,并提出一个在PAN过程中动眼神经麻痹的例子。材料和方法:使用检索PubMed数据库的术语“结节性多动脉炎”、“神经”、“动眼病”、“颅神经”和“颅神经病变”对描述所分析问题的文本进行评价。分析中只包括带有标题和摘要的英文全文文章。作为文章分析的指导方针,使用了个体患者数据系统评价原则(PRISMA-IPD)中描述的方法。结果:经文献筛选,仅16例PAN合并颅神经病变纳入分析。10例PAN的首发表现为颅神经病变,以累及视神经最为常见(62.5%);其中动眼神经受累3例。糖皮质激素和环磷酰胺治疗是最常见的。结论:颅神经病变,特别是动眼神经麻痹是PAN罕见的首发神经表现,但在鉴别诊断时应考虑这一临床问题。特别是有周围神经病变、一般症状、皮肤病变和乙型肝炎病毒感染的患者,在血管炎过程中应评估是否累及脑神经。在脑神经受累不明确的情况下,在鉴别诊断中也应考虑PAN作为症状的原因和疾病的第一表现。
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
Reumatologia
Reumatologia Medicine-Rheumatology
CiteScore
2.70
自引率
0.00%
发文量
44
审稿时长
10 weeks
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