在Stevens-Johnson综合征和中毒性表皮坏死松解的表皮中,髓过氧化物酶阳性的单核细胞多于cd3阳性的t淋巴细胞。

IF 3.1 3区 医学 Q1 PATHOLOGY
Masakazu Fujimoto, Yuki Teramoto, Kai Mizoguchi, Kodai Furuta, Hiroyuki Irie, Yo Kaku, Masahiro Hirata, Kenji Kabashima, Hironori Haga
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引用次数: 0

摘要

Stevens-Johnson综合征和中毒性表皮坏死松解症(SJS/TEN)是危及生命的粘膜皮肤疾病,传统上被认为是严重的T细胞介导的超敏反应。然而,最近的证据强调了髓过氧化物酶(MPO)在SJS/TEN发病机制中的潜在作用,MPO主要由中性粒细胞产生。在这里,我们检测了SJS/TEN患者(n = 15)皮肤活检标本中MPO的表达,以评估其诊断价值,并将其与多形性红斑(EM) (n = 8)和移植物抗宿主病(GVHD) (n = 10)患者的结果进行比较。所有SJS/TEN病例中均存在mpo阳性的单个核细胞,其数量往往超过cd3阳性T细胞(86.7%)。与GVHD患者相比,SJS/TEN患者MPO/CD3比值大于1的病例明显增多(p1是SJS/TEN的病理特征,但其特异性可能有限)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Myeloperoxidase-positive mononuclear cells predominate over CD3-positive T-lymphocytes in the epidermis of Stevens-Johnson syndrome and toxic epidermal necrolysis.

Stevens-Johnson syndrome and toxic epidermal necrolysis (SJS/TEN) are life-threatening mucocutaneous conditions traditionally regarded as severe T cell-mediated hypersensitivity reactions. However, recent evidence has highlighted the potential role of myeloperoxidase (MPO), primarily produced by neutrophils, in the pathogenesis of SJS/TEN. Here, we examined the expression of MPO in skin biopsy specimens from patients with SJS/TEN (n = 15) to evaluate its diagnostic utility, comparing the findings with those from patients with erythema multiforme (EM) (n = 8) and graft-versus-host disease (GVHD) (n = 10). MPO-positive mononuclear cells were present in all SJS/TEN cases, often outnumbering CD3-positive T cells (86.7%). A significantly higher number of cases with an MPO/CD3 ratio greater than 1 was observed in patients with SJS/TEN compared with that in patients with GVHD (p < 0.01). However, no such difference was observed between SJS/TEN and EM. These findings suggest that an MPO/CD3 > 1 is a pathologic feature of SJS/TEN; however, its specificity may be limited.

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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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