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16例线性IgA沉积患者经免疫电子显微镜检查诊断成人线状IgA皮病。

Diagnosis of adult linear IgA dermatosis by immunoelectronmicroscopy in 16 patients with linear IgA deposits.

作者信息

Prost C, De Leca A C, Combemale P, Labeille B, Martin N, Cosnes A, Guillaume J C, Venencie P Y, Verret J L, Dubertret L

机构信息

Department of Dermatology, Hôpital Henri Mondor, Créteil, France.

出版信息

J Invest Dermatol. 1989 Jan;92(1):39-45. doi: 10.1111/1523-1747.ep13070851.

DOI:10.1111/1523-1747.ep13070851
PMID:2642511
Abstract

Homogeneous linear IgA deposits at the dermo-epidermal junction (DEJ) shown by direct immunofluorescence are characteristic of what is termed linear IgA bullous dermatosis. However, it is not yet certain that this disease constitutes an entity distinct from other subepidermal blistering diseases, especially when IgG deposits are also present. Sixty-one cases of subepidermal blistering disease in adults were therefore investigated by immunoelectron microscopy (IEM), and the 16 patients observed to have homogeneous linear IgA deposits were compared with the 45 who had no IgA but had IgG and/or C3. In 11 of the 16 patients with IgA (four of whom also had IgG), the deposits were linear and formed a mirror image pattern on each side of the lamina densa from which they were separated by a clear space. In contrast to this monomorphic IEM pattern, clinical and other laboratory findings were very heterogeneous, making exact clinical diagnosis difficult. Of the remaining five patients in this group of sixteen, three (all with both IgA and IgG) had bullous pemphigoid, epidermolysis bullosa acquisita, and cicatricial pemphigoid, respectively, on IEM and clinical investigation. In the remaining two patients (one with both IgA and IgG, and one with IgA only) the deposits were located in the lamina lucida, making precise classification impossible. None of the 45 patients with isolated IgG and/or C3 deposition displayed the mirror image pattern. We conclude that this IEM pattern may constitute a specific diagnostic criterion of linear IgA dermatosis.

摘要

直接免疫荧光显示在真皮-表皮交界处(DEJ)有均匀线性IgA沉积是所谓线性IgA大疱性皮肤病的特征。然而,这种疾病是否构成一种与其他表皮下大疱性疾病不同的实体尚不确定,尤其是当也存在IgG沉积时。因此,我们通过免疫电子显微镜(IEM)对61例成人表皮下大疱性疾病进行了研究,并将观察到有均匀线性IgA沉积的16例患者与45例无IgA但有IgG和/或C3的患者进行了比较。在16例有IgA的患者中,有11例(其中4例也有IgG),沉积物呈线性,在致密板两侧形成镜像模式,它们与致密板之间有一个清晰的间隙。与这种单形性IEM模式形成对比的是,临床和其他实验室检查结果非常异质,使得准确的临床诊断很困难。在这16例患者中的其余5例中,3例(均同时有IgA和IgG)经IEM和临床检查分别诊断为大疱性类天疱疮、获得性大疱性表皮松解症和瘢痕性类天疱疮。在其余2例患者中(1例同时有IgA和IgG,1例仅有IgA),沉积物位于透明板内,无法进行精确分类。45例仅有IgG和/或C3沉积的患者均未表现出镜像模式。我们得出结论,这种IEM模式可能构成线性IgA皮肤病的一个特异性诊断标准。

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Diagnosis of adult linear IgA dermatosis by immunoelectronmicroscopy in 16 patients with linear IgA deposits.16例线性IgA沉积患者经免疫电子显微镜检查诊断成人线状IgA皮病。
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