Department of Dermatology, Mayo Clinic, Rochester, Minnesota, USA.
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
J Cutan Pathol. 2024 Dec;51(12):987-999. doi: 10.1111/cup.14722. Epub 2024 Sep 22.
Due to the immune-mediated nature of non-infectious cutaneous vasculitis, skin biopsy specimens are often submitted for direct immunofluorescence (DIF) testing when vasculitis is considered clinically. However, evidence regarding the clinical value of DIF has not been rigorously appraised.
In this scoping review, we aimed to systematically evaluate the peer-reviewed literature on the utility of DIF in vasculitis to assist with the development of appropriate use criteria by the American Society of Dermatopathology.
Two electronic databases were searched for articles on DIF and vasculitis (January 1975-October 2023). Relevant case series involving more than or equal to three patients, published in English, and with full-text availability were included. Additional articles were identified manually via reference review. Due to study heterogeneity, findings were analyzed descriptively.
Of 255 articles identified, 61 met the inclusion criteria. Cumulatively representing over 1000 DIF specimens, several studies estimated DIF sensitivity to be 75%. While vascular immunoglobulin A (IgA) deposits on DIF were associated with renal disease, other systemic associations were inconsistent. Vascular IgG deposition may be overrepresented in ANCA-associated vasculitis. Granular vascular and epidermal basement membrane zone Ig deposition differentiated hypocomplementemic from normocomplementemic urticarial vasculitis. Few studies have assessed the added value of DIF over routine microscopy alone in vasculitis.
This scoping review discovered that DIF testing for vasculitis has been performed not only for diagnostic confirmation of vasculitis but also for disease subtype classification and prediction of systemic associations. Future studies on test sensitivity of DIF compared to that of histopathology are needed.
由于非感染性皮肤血管炎的免疫介导性质,当临床上考虑血管炎时,通常会提交皮肤活检标本进行直接免疫荧光(DIF)检测。然而,关于 DIF 的临床价值的证据尚未经过严格评估。
在本次范围界定审查中,我们旨在系统评估 DIF 在血管炎中的效用的同行评议文献,以协助美国皮肤病理学会制定适当的使用标准。
两个电子数据库被搜索了有关 DIF 和血管炎的文章(1975 年 1 月至 2023 年 10 月)。纳入了涉及 3 例以上患者的、发表在英语期刊上且可提供全文的相关病例系列研究。通过参考文献审查手动确定了其他文章。由于研究存在异质性,因此分析结果为描述性的。
在 255 篇文章中,有 61 篇符合纳入标准。这些研究累计涉及超过 1000 例 DIF 标本,多项研究估计 DIF 的敏感性为 75%。虽然 DIF 上的血管免疫球蛋白 A(IgA)沉积物与肾脏疾病有关,但其他系统相关性并不一致。血管 IgG 沉积可能在抗中性粒细胞胞浆抗体相关性血管炎中更为突出。颗粒状血管和表皮基底膜带 Ig 沉积可区分低补体血症性与正常补体血症性荨麻疹性血管炎。很少有研究评估 DIF 检测在血管炎中的附加价值是否超过单独常规显微镜检查。
本次范围界定审查发现,DIF 检测不仅用于血管炎的诊断确认,还用于疾病亚型分类和预测系统相关性。需要进一步研究 DIF 与组织病理学相比的检测敏感性。