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类苔藓样糠疹型药物反应:10例临床组织病理学研究

Pityriasis lichenoides-like drug reaction: A clinical histopathologic study of 10 cases.

作者信息

Magro Cynthia, Guo Ruifeng, Nguyen Giang Huong, Tsang Hamilton, Momtahen Shabnam

机构信息

Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York.

出版信息

Dermatol Online J. 2017 Nov 15;23(11):13030/qt7xd8j71z.

Abstract

BACKGROUND

Lymphomatoid drug reactions can mimic endogenous T and B cell lymphoproliferative diseases.

OBJECTIVES

We present a novel form of cutaneous drug reaction with features of pityriasis lichenoides (PL), a recognized form of T cell dyscrasia.

METHODS

Ten cases were studied where a cutaneous eruption exhibiting semblance to PL within a few weeks to months after starting a particular drug.

RESULTS

The patient cohort comprised 7 females and 3 males with the mean age of 60 years. Widely distributederythematous cutaneous lesions were present in 6 cases whereas a more localized distribution was seen in three cases. The most frequently implicated drugsassociated with the eruption were antidepressants and statins. Histologic examination showed a morphologic picture identical to PL including marked epitheliotropism of mildly atypical lymphocytes, psoriasiform epidermal hyperplasia, dyskeratosis, hemorrhage, and a thick parakeratotic scale. Therewas a significant reduction in the expression of CD7 and CD62L amid the T cells. Regression of the eruption occurred in all cases excluding one.

CONCLUSION

Thefindings conform the categorization of this process as a form of T-cell dyscrasia albeit one that is reversible, dependent on the drug withdrawal. The limitationof our study includes the retrospective design of the study.

摘要

背景

淋巴瘤样药物反应可模仿内源性T和B细胞淋巴增殖性疾病。

目的

我们报告一种具有苔藓样糠疹(PL)特征的新型皮肤药物反应,PL是一种公认的T细胞发育异常形式。

方法

研究了10例患者,这些患者在开始使用某种特定药物后的几周至几个月内出现了类似PL的皮肤疹。

结果

患者队列包括7名女性和3名男性,平均年龄为60岁。6例出现广泛分布的红斑性皮肤病变,3例分布较局限。与皮疹最常相关的药物是抗抑郁药和他汀类药物。组织学检查显示形态学表现与PL相同,包括轻度非典型淋巴细胞的显著亲表皮性、银屑病样表皮增生、角化不良、出血和厚的不全角化鳞屑。T细胞中CD7和CD62L的表达显著降低。除1例患者外,所有病例的皮疹均消退。

结论

这些发现符合将该过程归类为一种T细胞发育异常的形式,尽管它是可逆的,取决于停药。我们研究的局限性包括研究的回顾性设计。

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