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口腔盘状红斑狼疮。III. 66例患者的组织病理学研究。

Oral discoid lupus erythematosus. III. A histopathologic study of sixty-six patients.

作者信息

Schiødt M

出版信息

Oral Surg Oral Med Oral Pathol. 1984 Mar;57(3):281-93. doi: 10.1016/0030-4220(84)90184-1.

DOI:10.1016/0030-4220(84)90184-1
PMID:6584819
Abstract

A detailed histopathologic study was conducted blindly on biopsy specimens from 66 patients with oral discoid lesions (oral DLE) mixed in random order with biopsy specimens from control groups of 25 cases of oral lichen planus (LP), 25 cases of oral leukoplakia, 13 cases with an uncertain diagnosis termed DLE? LP? and 7 cases of galvanic lesions related to amalgam fillings. Fifty-two histopathologic variables were examined, and a ranking was calculated for the variables that provided the best discrimination between the subgroups of clinically typical oral DLE and LP and between typical DLE and leukoplakia, respectively. Histopathologic variables not previously described in oral DLE but characteristic of this disease were identified: multinucleated epithelial cells containing three or more nuclei and the presence of epithelial islands in the connective tissue. Patients with systemic lupus erythematosus (SLE) in addition to oral DLE showed generally the same histopathologic features as those without SLE. The inflammatory infiltrates were slighter and more diffuse among the SLE patients as compared to the non-SLE patients. The simplest possible combination of histopathologic variables diagnostic for oral DLE consisted of the following five: (1) hyperkeratosis with keratotic plugs, (2) atrophy of the rete processes, (3) deep inflammatory infiltrate, (4) edema in the lamina propria, and (5) thick patchy or continuous PAS-positive juxtaepithelial deposits. This combination is suggested as new histopathologic criteria for oral DLE. These criteria were tested among clinically atypical cases of DLE and the other groups of mucosal lesions, with a sensitivity of 92% and a specificity of 96% against both LP and leukoplakia for the presence of two or more of the five criteria.

摘要

对66例口腔盘状病变(口腔盘状红斑狼疮,oral DLE)患者的活检标本进行了详细的组织病理学研究,这些标本与25例口腔扁平苔藓(LP)、25例口腔白斑、13例诊断不明确(称为DLE?LP?)以及7例与汞合金充填物相关的电损伤病例的活检标本随机混合。检查了52个组织病理学变量,并分别计算了能最佳区分临床典型口腔DLE和LP亚组以及典型DLE和白斑亚组的变量的排名。确定了以前未在口腔DLE中描述但为本病特征的组织病理学变量:含有三个或更多核的多核上皮细胞以及结缔组织中上皮岛的存在。除口腔DLE外还患有系统性红斑狼疮(SLE)的患者通常表现出与无SLE患者相同的组织病理学特征。与非SLE患者相比,SLE患者的炎症浸润更轻微且更弥漫。诊断口腔DLE的组织病理学变量的最简单可能组合包括以下五个:(1)伴有角化栓的角化过度,(2) rete突萎缩,(3)深部炎症浸润,(4)固有层水肿,(5)厚的斑片状或连续的PAS阳性上皮下沉积物。建议将此组合作为口腔DLE的新组织病理学标准。在DLE临床非典型病例和其他黏膜病变组中对这些标准进行了测试,对于存在五个标准中的两个或更多标准的情况,针对LP和白斑的敏感性为92%,特异性为96%。

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