Stephan Carla, Ma Linglei
Department of Pathology and Laboratory Medicine, Weill Cornell Medical Center, NewYork-Presbyterian, New York, NY 10065, USA.
Department of Pathology, University of Virginia, Charlottesville, VA 22903, USA.
Dermatopathology (Basel). 2024 Dec 19;11(4):377-382. doi: 10.3390/dermatopathology11040041.
The diagnostic utility of immunohistochemistry on paraffin-embedded sections in bullous disorders is useful when frozen tissue is not available. In pemphigus vulgaris and pemphigus foliaceus, an intercellular lace-like staining pattern of IgG4 on lesional tissue by immunohistochemistry has been described, with a comparable sensitivity and specificity to direct immunofluorescence on perilesional tissue. This study aimed to evaluate the staining pattern of IgG4 in non-immunobullous disorders to highlight the potential pitfalls when using this stain. In this study, we conducted a retrospective review of our institution's database of non-immunobullous disorders where immunohistochemistry of IgG4 was performed to rule out pemphigus. We identified 27 cases where IgG4 immunohistochemistry was performed and observed intercellular IgG4 staining in some cases of Grover disease, bullous impetigo, irritated dermal hypersensitivity reaction, acantholytic actinic keratosis, and graft versus host disease. Our results indicate that the interpretation of IgG4 staining by immunohistochemistry in cutaneous acantholytic disorders should be approached with caution. Confirmation on cryosections with direct immunofluorescence study results is important in these settings.
当无法获得冷冻组织时,免疫组化技术在石蜡包埋切片上对大疱性疾病的诊断具有重要作用。在寻常型天疱疮和落叶型天疱疮中,免疫组化显示病变组织上IgG4呈细胞间花边样染色模式,其敏感性和特异性与病损周围组织直接免疫荧光检查相当。本研究旨在评估IgG4在非免疫性大疱性疾病中的染色模式,以突出使用该染色时可能存在的陷阱。在本研究中,我们对本机构非免疫性大疱性疾病数据库进行了回顾性分析,这些病例均进行了IgG4免疫组化检查以排除天疱疮。我们确定了27例行IgG4免疫组化检查的病例,在某些Grover病、大疱性脓疱疮、刺激性皮肤过敏反应、棘层松解性光化性角化病和移植物抗宿主病病例中观察到细胞间IgG4染色。我们的结果表明,在皮肤棘层松解性疾病中,对免疫组化IgG4染色结果的解读应谨慎。在这些情况下,通过直接免疫荧光研究结果对冰冻切片进行确认很重要。