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嗜酸性粒细胞增多综合征1例 被引量:4

A Case of Hyperosinophilic Syndrome
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摘要 患者男,65岁。全身反复出现红斑和丘疹,伴瘙痒5年,加重2周。伴心、肝和肺多器官功能损害。骨髓及外周血嗜酸性粒细胞明显增多。诊断:嗜酸性粒细胞增多综合征。予糖皮质激素、雷公藤多甙及对症支持治疗半月后,症状明显好转。 A-65-year-old male was referred to our hospital with a 5 years history of recurrent itchy erythematous papule on the entire body, associated with multiple organ damage in heart, liver and lung. These skin lesions had aggravated two weeks before. The eosinophils on the bone marrow and peripheral blood smears showed marked elevation. Thus, a clinical diagnosis of hypereosinophilia syndrome was made. The patient obtained after had been treated with oral glucocorticoids, Tripterygium wilfordii and supporting therapy for two weeks clinical improvement.
出处 《中国皮肤性病学杂志》 CAS 北大核心 2012年第1期64-65,共2页 The Chinese Journal of Dermatovenereology
关键词 嗜酸性粒细胞增多综合征 糖皮质激素 雷公藤多甙 Hypereosinophilia syndrome Glucocorticoids Glucosida tripterygii
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参考文献4

  • 1Offidani A, Bemardini ML,Simonetti O,et al. Hypereosinophilie dermatosis: skin lesions as the only manifestation of the idiopathic hypereosinophilic syndrome? [J]. Br J Dermatol,2000,143 ( 3 ) : 675-677.
  • 2Song HS, Park SK. A case of monosomy-7 eosinophilie leukemia and neurofibromatosis,terminated with disseminated cryptococcosis[ J ]. Korean J Intern Med ,1987,2( 1 ) :131-134.
  • 3Yoon TY,Ahn GB, Chang SH. Complete remission of hyperensinophilic syndrome after interferon-alpha therapy : report of a ease and literature review[ J ]. J Dermatol,2000,27 (2) : 110-115.
  • 4Schaller JL,Burkland GA. Case report:rapid and complete control of idiopathic hypereosinophilia with imatinib mesylate [J]. Med Gen Med, 2001,3(5) :9.

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