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在使用超强效外用类固醇和甲氨蝶呤治疗大疱性类天疱疮期间发生的皮肤卡波西肉瘤:三例报告

Cutaneous Kaposi sarcoma during treatment with superpotent topical steroids and methotrexate for bullous pemphigoid: three cases.

作者信息

Binois Raphaëlle, Nadal Marion, Esteve Eric, De Muret Anne, Kerdraon Rémy, Gheit Tarik, Tommasino Massimo, Gaboriaud Pauline, Touze Antoine, Samimi Mahtab

机构信息

University François Rabelais, Boulevard Tonnelé, 37044 Tours Cedex 9, France, Department of Dermatology, Hospital of Orléans, 1 rue Porte Madeleine, 45032 Orléans, France.

University François Rabelais, Boulevard Tonnelé, 37044 Tours Cedex 9, France, Department of Dermatology, Hospital of Tours, Avenue de la République, 37044 Tours Cedex 9, France.

出版信息

Eur J Dermatol. 2017 Aug 1;27(4):369-374. doi: 10.1684/ejd.2017.3027.

Abstract

Iatrogenic Kaposi sarcoma (KS) has previously been reported in patients with bullous pemphigoid (BP), in relation to systemic steroids. To report three cases of previously unreported cutaneous KS during treatment with superpotent topical steroids (STS) and methotrexate (MTX). All patients were elderly men with BP treated with STS for 2 to 32 months (cumulative doses: 2,700-9,150 g) before MTX was introduced (dosage: 10-12.5 mg/week). KS occurred one to nine months after the combined therapy. In one case, KS rapidly resolved after withdrawal of MTX. In two cases, vinblastine and/or radiotherapy were required to achieve regression of KS. Human herpes virus 8 (HHV8) latency-associated nuclear antigen was not expressed in BP lesions biopsied prior to development of KS (n = 3), but HHV8 DNA was detected in BP lesions from the patient with the most aggressive KS. Several predisposing factors were identified, including sex and age, high cumulative doses of STS, combination with MTX, and impaired immune status. In such cases, serum antibodies against HHV8 infection may be investigated in BP patients before introduction of MTX in order to guide clinical monitoring.

摘要

医源性卡波西肉瘤(KS)此前曾在大疱性类天疱疮(BP)患者中被报道,与全身用类固醇有关。本文报告3例在强效外用类固醇(STS)和甲氨蝶呤(MTX)治疗期间出现的此前未报道过的皮肤KS病例。所有患者均为老年男性,患有BP,在引入MTX(剂量:10 - 12.5mg/周)之前,接受STS治疗2至32个月(累积剂量:2700 - 9150g)。联合治疗后1至9个月出现KS。1例患者在停用MTX后KS迅速消退。2例患者需要长春花碱和/或放疗才能使KS消退。在KS发生前活检的BP皮损中未检测到人疱疹病毒8(HHV8)潜伏相关核抗原(n = 3),但在KS最严重的患者的BP皮损中检测到HHV8 DNA。确定了几个易感因素,包括性别和年龄、STS的高累积剂量、与MTX联合使用以及免疫状态受损。在这种情况下,在引入MTX之前,可对BP患者进行HHV8感染血清抗体检测,以指导临床监测。

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