Hitchins L, Fucich L F, Freeman S M, Millikan L E, Marrogi A J
Department of Pathology, Tulane University School of Medicine, New Orleans, LA, USA.
J Investig Med. 1997 Oct;45(8):463-8.
Lichen planus (LP) and the lichenoid variant of chronic graft-versus-host disease (cGVHD) can present with similar clinical and histological findings. The distinction, although difficult, is important both prognostically and therapeutically. The mechanism and effector cell phenotypes have also shown to differ between the 2 entities. While the lichenoid infiltrate of LP is predominantly T lymphocytes helper/inducer cell phenotype, the suppressor/cytotoxic subset appears to play a major role in cGVHD. The aim of this study is to determine whether the immunophenotypic character of the lichenoid infiltrate can aid in distinguishing the 2 entities.
Biopsies were obtained from 2 patients with lichenoid papules and a history of transplantation. Light microscopy revealed lichenoid inflammation in both cases characterized by a band-like lymphohistiocytic infiltrate at the dermal-epidermal junction. Immunochemistry was performed on fresh tissue using a panel of monoclonal antibodies including anti-CD1a, CD3, CD4, CD8, CD16, CD20, CD28, and CD68. Results were quantitated using computer-assisted image analysis.
We found that in both cases the majority of cells stained with pan T cell marker CD3+. One case demonstrated predominantly CD4+ T cells and increased numbers of CD1a positive Langerhans cells, while the lymphokine natural killer cell activity (LAK) markers anti-CD16 and anti-CD28 were largely nonreactive. Conversely, the second case contained predominately CD8+ lymphocytes and very few CD1a positive Langerhans cells with abundant LAK cell anti-CD16 and anti-CD28 reactivity.
Based on these findings, the former was classified as lichen planus and the latter as lichenoid cGVHD. The diagnoses are substantiated with clinical history and follow-up information. We conclude that immunophenotypic characteristics of the infiltrate can be a useful tool in differentiating lichenoid cGVHD from lichen planus.
扁平苔藓(LP)和慢性移植物抗宿主病(cGVHD)的苔藓样变体可呈现相似的临床和组织学表现。尽管区分困难,但在预后和治疗方面都很重要。这两种疾病的机制和效应细胞表型也有所不同。LP的苔藓样浸润主要是T淋巴细胞辅助/诱导细胞表型,而抑制/细胞毒性亚群似乎在cGVHD中起主要作用。本研究的目的是确定苔藓样浸润的免疫表型特征是否有助于区分这两种疾病。
从2例有苔藓样丘疹且有移植史的患者身上获取活检组织。光学显微镜检查显示两例均有苔藓样炎症,其特征为真皮-表皮交界处有条带状淋巴细胞-组织细胞浸润。使用一组单克隆抗体,包括抗CD1a、CD3、CD4、CD8、CD16、CD20、CD28和CD68,对新鲜组织进行免疫化学检测。结果采用计算机辅助图像分析进行定量。
我们发现,两例中大多数细胞均被泛T细胞标志物CD3+染色。其中一例主要为CD4+T细胞,且CD1a阳性朗格汉斯细胞数量增加,而淋巴因子自然杀伤细胞活性(LAK)标志物抗CD16和抗CD28大多无反应。相反,第二例主要为CD8+淋巴细胞,CD1a阳性朗格汉斯细胞极少,且LAK细胞抗CD16和抗CD28反应性丰富。
基于这些发现,前者被归类为扁平苔藓,后者被归类为苔藓样cGVHD。诊断通过临床病史和随访信息得到证实。我们得出结论,浸润的免疫表型特征可作为区分苔藓样cGVHD和扁平苔藓的有用工具。