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自身免疫性大疱性皮肤病的诊断:在病灶组织和病灶周围冷冻皮肤样本中使用 C4d、C3d、IgG 和 IgG4 进行免疫组织化学染色的对比分析。

Diagnosis of autoimmune bullous dermatoses: Comparative analysis of immunohistochemical staining using C4d, C3d, IgG, and IgG4 in lesional tissues and perilesional frozen skin samples.

机构信息

Tekirdağ Namık Kemal University Medical Faculty, Pathology Department, Tekirdağ, Turkey.

Tekirdağ Namık Kemal University Medical Faculty, Dermatology and Venereology Department, Tekirdağ, Turkey.

出版信息

Ann Diagn Pathol. 2024 Dec;73:152367. doi: 10.1016/j.anndiagpath.2024.152367. Epub 2024 Aug 22.

Abstract

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.

摘要

免疫组织化学染色法检测免疫球蛋白和补体有助于诊断临床和组织学检查结果与自身免疫性大疱性皮肤病(AIBD)一致的患者。我们旨在研究免疫组织化学标志物在 AIBD 病变活检和病变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,根据初步诊断为 AIBD 收集病变活检和病变周围样本的 136 例患者。尽管直接免疫荧光(DIF)检查结果被认为是优先考虑的,但所有诊断均通过评估临床、组织病理学和血清学发现以及 DIF 结果(与临床诊断一致的 C3、IgG、IgA 或 IgM 阳性)来共同确认。在确认诊断后,将样本分为 AIBD 或其他。同时为 DIF 采集的病变周围组织在 -80°C 下冷冻,并解冻,制备 FFPE 组织。我们对病变和病变周围样本的 FFPE 组织进行了免疫组织化学染色(C4d、C3d、IgG 和 IgG4)。在表皮真皮交界处或表皮水疱空间出现强线性或颗粒状染色模式被认为与病例诊断相符。AIBD 以外的病例被用作阴性对照组织,以评估免疫组织化学标志物的特异性。在 136 例病例中,52 例被诊断为 AIBD。在病变样本中,C4d、C3d、IgG 和 IgG4 的敏感性分别为 80.6%、69.4%、75%和 5.7%,相应的特异性分别为 100%、98.7%、89.6%和 97.4%,与天疱疮疾病相比,天疱疮疾病的敏感性分别为 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,我们检测到的表达数量有限。C4d、C3d、IgG 和 IgG4 的敏感性分别为 8.7%、2.2%、19.4%和 2.2%,相应的特异性分别为 100%、100%、98.5%和 98.6%。病变组织和病变周围冷冻样本的免疫组化结果之间存在无到轻微的一致性。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)。从病变处采集的活检样本进行 C4d、C3d、IgG 和 IgG4 的免疫组织化学染色可能有助于 AIBD 的诊断,从而无需进行额外的活检并加速诊断过程。

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