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一名发作性血管性水肿伴嗜酸性粒细胞增多综合征患者血清白细胞介素-5水平升高。

Increased serum level of interleukin-5 in a patient with episodic angioedema and eosinophilia syndrome.

作者信息

Murakami T, Kato J, Kogawa K, Watanabe N, Sakamaki S, Kohgo Y, Hamabe K, Ishiyama N, Enokihara H, Niitsu Y

机构信息

Department of Internal Medicine (Section 4), Sapporo Medical College, Japan.

出版信息

Intern Med. 1993 Apr;32(4):343-5. doi: 10.2169/internalmedicine.32.343.

Abstract

A case of episodic angioedema and eosinophilia syndrome is reported. An 18-year-old male suffered from monthly episodes of angioedema, pruritic papules, weight gain, and fever for twelve years. During the episodes, peripheral eosinophils and serum levels of interleukin (IL)-5, an eosinophil proliferating cytokine were elevated. Extensive evaluations disclosed neither visceral involvement nor evidence of parasitic infections, collagen diseases, or neoplastic disorders. Corticosteroid treatment brought about a dramatic clinical improvement concomitant with decrement of eosinophils and serum IL-5 was observed. These observations suggest that IL-5 may be a causative factor for this pathological state.

摘要

报告了一例发作性血管性水肿和嗜酸性粒细胞增多综合征病例。一名18岁男性,12年来每月发作血管性水肿、瘙痒性丘疹、体重增加和发热。发作期间,外周嗜酸性粒细胞以及嗜酸性粒细胞增殖细胞因子白细胞介素(IL)-5的血清水平升高。广泛评估未发现内脏受累,也未发现寄生虫感染、胶原病或肿瘤性疾病的证据。皮质类固醇治疗带来了显著的临床改善,同时观察到嗜酸性粒细胞减少以及血清IL-5下降。这些观察结果表明,IL-5可能是这种病理状态的致病因素。

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