坏死的角质形成细胞可能有助于牛皮癣的诊断和发病机制吗?

IF 2.5 4区 医学 Q2 DERMATOLOGY Dermatology practical & conceptual Pub Date : 2024-07-01 DOI:10.5826/dpc.1403a213
Bengü Çevirgen Cemil, Aysun Gökçe, Gamze Taş Aygar, Selda Pelin Kartal
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引用次数: 0

摘要

导言:能够识别高风险面部基底细胞癌(BCC)可能会减少不完全切除和不适当的治疗:我们试图研究预测面部 BCC 亚型的临床和皮肤镜标准,分析读者之间的观察者间一致性,并开发一种诊断算法来预测高风险组织病理学亚型:在这项单中心回顾性调查中,6位独立读者评估了经组织病理学验证的原发性面部BCC图像中预定义的临床和皮肤镜标准,包括:地形、边界分界、血管、溃疡、白瓷区、发亮的白色斑点和条纹,以及溃疡内的色素结构和血管:共分析了 297 对临床和皮肤镜图像。与高风险亚型关系最密切的是"凹凸不平 "的地形(OR 3.8,95% CI,3.1-4.7)、边界不清晰(OR 3.4,95% CI 3.1-4.7)、白瓷区域(OR 3.5,95% CI 2.8-4.5)和溃疡内的血管(OR 3.1,95% CI 2.4-4.1)。主要集中的血管是结节型(OR 1.7,95% CI 1.3-2.2)或高危型(OR 2.0,95% CI 1.6-2.5)亚型的阳性诊断标准,是浅表 BCC 的强阴性诊断标准(OR 14.0,95% CI 9.6-20.8)。观察者之间的一致性从一般到相当高(κ=0.36 到 0.72)不等。基于这些结果的诊断算法显示,预测高风险 BCC 亚型的灵敏度为 81.4%(95% CI,78.9-83.7%),特异度为 53.3%(95% CI,49.7-56.9%):综合临床和皮肤镜特征(包括地形和溃疡内血管等新特征)对于改善面部 BCC 亚型预测和管理决策至关重要。
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Might Necrotic Keratinocytes Contribute to the Diagnosis and Pathogenesis of Psoriasis?

Introduction: Psoriasis is a chronic inflammatory skin disease that can pose challenges for histopathological diagnosis. Recent research has emphasized the importance of necrotic keratinocytes, meaning keratinocytes undergoing programmed cell death, for diagnosing psoriasis. It has also become increasingly evident that programmed cell death pathways play a significant role in psoriasis's pathogenesis, development, and progression, including via a recently identified programmed cell death mechanism called "PANoptosis."

Objectives: In our study, we aimed to investigate the significance of necrotic keratinocytes in both the diagnosis and pathogenesis of psoriasis.

Methods: We analyzed the number of necrotic keratinocytes in 135 samples of psoriasis, 57 samples of psoriasiform spongiotic dermatitis, and 71 samples of normal skin. We additionally assessed the distribution of necrotic keratinocytes in the upper, middle, and lower thirds of the epidermis.

Results: Our findings revealed a significant difference in the total number of necrotic keratinocytes and their distribution within epidermal regions between patients with psoriasis and both the psoriasiform spongiotic dermatitis and control groups (p < .001). In particular, necrotic keratinocytes were predominantly found in the upper epidermis (77.5%) in patients with psoriasis. We also observed a strong correlation between Psoriasis Area and Severity Index scores and the total count of necrotic keratinocytes in patients with psoriasis (r = .72).

Conclusions: Our results highlight the role of necrotic keratinocytes, resulting from programmed cell death, as important marker cells in both the diagnosis and pathogenesis of psoriasis.

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