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[T细胞免疫缺陷中面部孔窍的增殖性脓皮病]

[Pyoderma vegetans of facial orifices in T-cell immunodeficiency].

作者信息

Hornstein O P, Djawari D

出版信息

Hautarzt. 1984 Mar;35(3):132-7.

PMID:6609152
Abstract

This is a report of a 24-year follow-up of a man now 33 years of age, who suffers almost continuously from severe inflammatory lesions of the lips, nose and eyelids, with increased susceptibility to respiratory infections since early childhood. The condition, previously described as "pyo-rhino-blepharo-stomatitis vegetans (McCarthy)", was treated with systemic corticosteroids and antimicrobial agents for years, but failed to improve until the immune status of the patient was checked after withdrawal of the steroids. T lymphocytes were found to be abnormal as to count in peripheral blood and various functional qualities determined in vivo and in vitro. For treatment, levamisole and thymopoietin pentapeptide (TP-5) were given. Subsequently each drug induced rapid and complete clearing of all lesions, but was followed by the recurrence of facial periorificial lesions after drug withdrawal. Change of the regimen by administering either inosiplex orally or commercial calf thymus extract parenterally, remained ineffective. During therapy with levamisole as well as TP-5, the number of T lymphocytes in peripheral blood normalized, yet impaired functions failed to improve. There was an elevated ratio of T-suppressor/T-inducer cells in blood using OKT antibodies. In vitro testing of different functions of polymorphonuclear leucocytes revealed normal results except for a slight decrease of chemotactic activity during levamisole. In view of the long clinical course, the mass of clinical and immunological data collected over decades, and the therapeutic results as a whole, the disease can be characterized as a peculiar type of pluriorificial pyoderma vegetans, caused by a distinct immunodeficiency of T lymphocytes.

摘要

这是一份对一名现年33岁男性患者进行24年随访的报告。该患者自童年早期起就几乎持续患有唇部、鼻部和眼睑的严重炎症性病变,且易患呼吸道感染。这种疾病先前被描述为“脓性鼻睑口炎(麦卡锡型)”,多年来一直使用全身性皮质类固醇和抗菌药物治疗,但直到停用类固醇后检查患者的免疫状态,病情才有所改善。发现患者外周血中的T淋巴细胞计数以及体内和体外测定的各种功能特性均异常。治疗时给予了左旋咪唑和胸腺生成素五肽(TP - 5)。随后,每种药物都使所有病变迅速完全消退,但停药后面部口周病变复发。改为口服肌苷或注射商业小牛胸腺提取物的治疗方案均无效。在使用左旋咪唑以及TP - 5治疗期间,外周血中的T淋巴细胞数量恢复正常,但受损的功能未能改善。使用OKT抗体检测发现血液中T抑制细胞/T诱导细胞的比例升高。对多形核白细胞不同功能的体外检测显示结果正常,只是在使用左旋咪唑期间趋化活性略有下降。鉴于其漫长的临床病程、数十年来收集的大量临床和免疫学数据以及整体治疗结果,该疾病可被表征为一种由T淋巴细胞明显免疫缺陷引起的特殊类型的多口周脓疱性增殖性皮炎。

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