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[放疗诱发的泛发性大疱性类天疱疮]

[Generalized bullous pemphigoid induced by radiotherapy].

作者信息

Srifi N, Benomar S, Zaghba N, Qasmi S, Senouci K, Elgueddari B, Hassam B, Ismaili N

机构信息

Service de dermatologie, CHU Ibn-Sina, Rabat, Maroc.

出版信息

Ann Dermatol Venereol. 2011;138(4):311-4. doi: 10.1016/j.annder.2010.11.016. Epub 2011 Jan 13.

Abstract

BACKGROUND

There have been a very small number of reported cases of radiotherapy-induced autoimmune bullous disease. We describe a case of generalised autoimmune sub-epidermal bullous pemphigoid (BP) induced by radiotherapy in a female patient presenting squamous cell carcinoma of the vulva.

CASE REPORT

In June 2008, a 48-year-old woman underwent vulvectomy with lymph node curettage for squamous cell carcinoma of the vulva. Following surgery, adjuvant radiotherapy was indicated. At the 16th session (dose of 32 Gy), erythema occurred on the irradiation field. At the 23rd session (46 Gy), the patient presented bullous lesions that became generalised after four days with involvement of the oral mucosa. Skin biopsy revealed sub-epidermal bullae and direct immunofluorescence showed continuous linear deposits of IgG and of C3 along the dermal-epidermal junction. Indirect immunofluorescence revealed the presence of antibodies directed against the basement membrane. A favourable outcome was achieved under systemic corticosteroids. No immunotransfer analysis of serum or any other immunological investigations were performed.

DISCUSSION

The clinical and histological features of this autoimmune bullous disease were evocative of BP, despite the absence of any formal proof. Radio-induced BP is extremely rare, with only 28 cases being described to date in the literature. The trigger mechanism is poorly understood; radiotherapy appears to cause changes in the antigenic properties of proteins in the dermal-epidermal junction resulting in production of autoantibodies. The radio-induced nature of BP does not affect therapeutic response. The case we report is novel in terms of both generalisation of the eruption and mucosal involvement.

摘要

背景

放射治疗诱发的自身免疫性大疱性疾病的报道病例数量极少。我们描述了一例因放疗诱发的全身性自身免疫性表皮下大疱性类天疱疮(BP),患者为一名患有外阴鳞状细胞癌的女性。

病例报告

2008年6月,一名48岁女性因外阴鳞状细胞癌接受了外阴切除术及淋巴结刮除术。术后,需进行辅助放疗。在第16次放疗(剂量为32 Gy)时,照射部位出现红斑。在第23次放疗(46 Gy)时,患者出现水疱性皮损,4天后皮损泛发并累及口腔黏膜。皮肤活检显示表皮下大疱,直接免疫荧光显示IgG和C3沿真皮-表皮交界处呈连续线性沉积。间接免疫荧光显示存在针对基底膜的抗体。在全身使用皮质类固醇激素治疗下取得了良好疗效。未进行血清免疫转移分析或任何其他免疫学检查。

讨论

尽管缺乏任何正式证据,但这种自身免疫性大疱性疾病的临床和组织学特征提示为BP。放射性诱发的BP极为罕见,迄今为止文献中仅描述了28例。触发机制尚不清楚;放疗似乎导致真皮-表皮交界处蛋白质的抗原特性发生变化,从而产生自身抗体。BP的放射性诱发性质并不影响治疗反应。我们报告的该病例在皮疹泛发和黏膜受累方面均具有独特性。

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