自身免疫性大疱性皮肤病的诊断:使用 C4d、C3d、IgG 和 IgG4 对病变组织和周围冷冻皮肤样本进行免疫组化染色的比较分析

IF 1.5 4区 医学 Q3 PATHOLOGY Annals of Diagnostic Pathology Pub Date : 2024-08-22 DOI:10.1016/j.anndiagpath.2024.152367
Sevil Karabağ , Özge Zorlu
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引用次数: 0

摘要

免疫球蛋白和补体的免疫组化染色可帮助诊断临床和组织学结果与自身免疫性大疱性皮肤病(AIBD)一致的患者。我们的目的是研究免疫组化标记物在 AIBD 皮损活检和皮损周围冷冻样本中的诊断价值。我们纳入了2019年1月至2023年1月期间收集的136例初步诊断为AIBD的皮损活检和韧带周围直接免疫荧光(DIF)检查样本。通过评估临床、组织病理学和血清学结果以及 DIF 结果(与临床诊断相符的 C3、IgG、IgA 或 IgM 阳性),对所有诊断进行了再次确认,但 DIF 结果被视为优先事项。确诊后,样本被归类为 AIBD 或其他。解冻与皮肤活检同时获得的 DIF 周围组织,并将其保存在 -80 °C,然后制备 FFPE 组织。我们对病变和韧带周围样本的 FFPE 组织进行了免疫组化染色(C4d、C3d、IgG 和 IgG4)。根据病例的诊断,真皮表皮交界处或表皮内水疱间隙的强线性或颗粒状染色模式被视为阳性。AIBD以外的病例作为阴性对照组织,以评估免疫组化标记物的特异性。在 136 例病例中,52 例被确诊为 AIBD。在皮损样本中,C4d、C3d、IgG和IgG4对丘疹性荨麻疹的敏感性分别为80.6%、69.4%、75%和5.7%,特异性分别为100%、98.7%、89.6%和97.4%,而对丘疹性荨麻疹的敏感性分别为18.2%、9.1%、70%和9.1%,特异性分别为98.7%、100%、89.6%和97.4%。在冷冻样本中,我们只在少数病例中检测到表达。C4d、C3d、IgG和IgG4的敏感性分别为8.7%、2.2%、19.4%和2.2%,特异性分别为100%、100%、98.5%和98.6%。病变组织和周围冷冻样本的 IHC 结果之间的一致性从无到有。C4d、C3d、IgG和IgG4的Kappa系数分别为0.120(P = 0.029)、0.111(P = 0.050)、0.203(P = 0.003)和- 0.15(P = 0.846)。用 C4d、C3d、IgG 和 IgG4 对从病变部位采集的活检样本进行免疫组化染色可指导 AIBD 的诊断,从而无需再进行活检并加快诊断过程。
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Diagnosis of autoimmune bullous dermatoses: Comparative analysis of immunohistochemical staining using C4d, C3d, IgG, and IgG4 in lesional tissues and perilesional frozen skin samples

Immunohistochemical staining with immunoglobulins and complements may aid the diagnosis of patients whose clinical and histological findings are consistent with autoimmune bullous dermatoses (AIBD). We aimed to investigate the diagnostic value of immunohistochemical markers in lesional biopsy and perilesional frozen samples in AIBD. We included 136 cases from whom lesional biopsies and perilesional samples for direct immunofluorescence (DIF) examination were collected with a preliminary diagnosis of AIBD between January 2019 and January 2023. All diagnoses were reconfirmed by evaluating the clinical, histopathological, and serological findings and DIF results (C3, IgG, IgA, or IgM positivity compatible with the clinical diagnosis) altogether, although DIF results were considered a priority. After confirming the diagnoses, the samples were categorized as AIBD or the others. The perilesional tissues obtained for DIF simultaneously with skin biopsy and stored at −80 °C were thawed, and FFPE tissues were prepared. We performed immunohistochemical staining (C4d, C3d, IgG, and IgG4) on FFPE tissues of both lesional and perilesional samples. Strong, linear, or granular staining patterns at the dermoepidermal junction or the intraepidermal blistering space were considered positive in line with the diagnosis of the case. Cases other than AIBD were used as negative control tissues to assess the specificity of immunohistochemical markers. Of the 136 cases, 52 were diagnosed with AIBD. In lesional samples, the sensitivity of C4d, C3d, IgG, and IgG4 was 80.6 %, 69.4 %, 75 %, and 5.7 % with corresponding specificity of 100 %, 98.7 %, 89.6 %, and 97.4 %, respectively in pemphigoid diseases compared to a sensitivity of 18.2 %, 9.1 %, 70 %, and 9.1 % and specificity of 98.7 %, 100 %, 89.6 %, and 97.4 %, respectively in pemphigus diseases. In frozen samples, we detected expression in a limited number of cases. The sensitivity of C4d, C3d, IgG, and IgG4 was 8.7 %, 2.2 %, 19.4 %, and 2.2 %, with corresponding specificity of 100 %, 100 %, 98.5 %, and 98.6, respectively. There was a none to slight concordance rate between the IHC results of lesional tissues and perilesional frozen samples. Kappa coefficients for C4d, C3d, IgG, and IgG4 were 0.120 (P = 0.029), 0.111 (P = 0.050), 0.203 (P = 0.003), and - 0.15 (P = 0.846), respectively. Immunohistochemical staining with C4d, C3d, IgG, and IgG4 on biopsy samples collected from lesions may guide the diagnosis of AIBD, thereby eliminating the need for an additional biopsy and accelerating the diagnostic process.

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来源期刊
CiteScore
3.90
自引率
5.00%
发文量
149
审稿时长
26 days
期刊介绍: A peer-reviewed journal devoted to the publication of articles dealing with traditional morphologic studies using standard diagnostic techniques and stressing clinicopathological correlations and scientific observation of relevance to the daily practice of pathology. Special features include pathologic-radiologic correlations and pathologic-cytologic correlations.
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