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累及颅底的特发性嗜酸性粒细胞增多综合征

Idiopathic hypereosinophilic syndrome with skull base involvement.

作者信息

Battineni M L, Galetta S L, Oh J, Lango M, Brooks J J, Schuster S J, Loevner L A

机构信息

Department of Radiology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.

出版信息

AJNR Am J Neuroradiol. 2007 May;28(5):971-3.

Abstract

Idiopathic hypereosinophilic syndrome (HES) is a heterogeneous disorder characterized by prolonged eosinophilia without an identifiable cause, ultimately resulting in organ dysfunction. Three major types of neurologic involvement have been well defined in HES; however, to our knowledge, inflammatory pseudotumor (IPT) in association with HES has not been reported. We present a case of IPT of the skull base in a patient with HES that suggests that HES may result in an exaggerated immunologic or inflammatory response leading to the formation of IPT.

摘要

特发性嗜酸性粒细胞增多综合征(HES)是一种异质性疾病,其特征为嗜酸性粒细胞增多且持续时间较长,病因不明,最终导致器官功能障碍。HES中已明确有三种主要的神经系统受累类型;然而,据我们所知,与HES相关的炎性假瘤(IPT)尚未见报道。我们报告一例HES患者发生颅底IPT的病例,提示HES可能导致过度的免疫或炎症反应,进而导致IPT的形成。

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本文引用的文献

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