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伴有嗜酸性粒细胞增多的播散性血管淋巴样增生:一例报告

Disseminated angiolymphoid hyperplasia with eosinophilia: a case report.

作者信息

Zhang Guo-Yi, Jiang Juan, Lin Tong, Wang Qian-Qiu

机构信息

Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, People's Republic of China.

出版信息

Cutis. 2003 Oct;72(4):323-6.

PMID:14604086
Abstract

A 37-year-old Cantonese man presented with pruritic erythematous papules and nodules on his face, limbs, and trunk that had been present for 10 years and aggravated for 2 years. More nodules were noticed where the skin was scratched and traumatized. The lesions were alleviated temporarily, but they did not subside entirely without therapy. The lesions responded to treatment with intravenous dexamethasone. Histopathology results indicated angiolymphoid hyperplasia with eosinophilia (ALHE), and the patient was diagnosed with disseminated ALHE (DALHE). His lesions ameliorated after treatment with prednisone.

摘要

一名37岁的广东男性,面部、四肢及躯干出现瘙痒性红斑丘疹和结节10年,近2年加重。在皮肤搔抓和外伤处可见更多结节。皮损经治疗可暂时缓解,但未经治疗则不会完全消退。静脉注射地塞米松治疗有效。组织病理学结果提示嗜酸性粒细胞增多性血管淋巴样增生(ALHE),该患者被诊断为播散性ALHE(DALHE)。泼尼松治疗后皮损改善。

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引用本文的文献

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Angiolymphoid hyperplasia with eosinophilia developing in a patient with history of peripheral T-cell lymphoma: evidence for multicentric T-cell lymphoproliferative process.患者外周 T 细胞淋巴瘤病史后发生血管淋巴样增生伴嗜酸性粒细胞增多:多中心 T 细胞淋巴增生过程的证据。
Diagn Pathol. 2008 May 29;3:22. doi: 10.1186/1746-1596-3-22.