Department of Dermatopathology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Autoimmune Bullous Disease Research Center, Department of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Int J Dermatol. 2019 Jul;58(7):825-829. doi: 10.1111/ijd.14387. Epub 2019 Jan 28.
Urticarial vasculitis (UV) is a clinicopathologic entity in which skin lesions resemble urticaria clinically but last more than 24 hours and resolve with residual purpura. In this study, we evaluated distinguishing histological features of UV from common urticaria to differentiate between these two entities.
During 1 year, 55 urticaria and 245 UV samples were assessed. The selection criteria for UV included: (1) samples that the histological diagnosis was confirmed by two independent dermatopathologists, (2) the histological diagnosis of UV was inconsistent with the first clinical impression and lesion characteristics.
Of our 245 UV patients, 96% had endothelial swelling, 18% had red blood cell (RBC) extravasation, neutrophilic infiltration was seen in 46.7%, and perivascular, interstitial, and perineural eosinophilic infiltration in 198 (81.8%), 181 (74.2%), and 118 (48.1%), respectively. Among different histological findings, endothelial cell swelling as well as neutrophil around vessels and eosinophilic infiltrations were statistically different between two groups (P-value ˂ 0.001). Both urticaria and UV samples showed a predominantly lymphocytic infiltration more than 10 cells per high power field (HPF) (98.2% of urticaria, 98.8% of UV), and only two patients (0.8%) with UV had predominant neutrophilic infiltration (more than 10 cells/HPF).
We have found that both urticaria and UV showed a predominantly lymphocytic infiltration along with RBC extravasation, endothelial cell swelling, and fibrin deposition in UV. Moreover, significant perineural, perivascular, and interstitial infiltration of eosinophil in UV lesions compared to urticaria was another point that indicates special contribution of these cells in UV pathogenesis.
荨麻疹性血管炎(UV)是一种临床病理实体,其皮肤病变在临床上类似于荨麻疹,但持续时间超过 24 小时,并伴有残余紫癜消退。在这项研究中,我们评估了 UV 与常见荨麻疹的组织学特征,以区分这两种实体。
在 1 年内评估了 55 例荨麻疹和 245 例 UV 样本。UV 的选择标准包括:(1)由两位独立的皮肤科病理学家确认的组织学诊断;(2)UV 的组织学诊断与最初的临床印象和病变特征不一致。
在我们的 245 例 UV 患者中,96%有内皮细胞肿胀,18%有红细胞(RBC)外渗,中性粒细胞浸润见于 46.7%,血管周围、间质和神经周围嗜酸性粒细胞浸润分别见于 198(81.8%)、181(74.2%)和 118(48.1%)。在不同的组织学发现中,内皮细胞肿胀以及血管周围和嗜酸性粒细胞浸润在两组之间存在统计学差异(P 值均<0.001)。荨麻疹和 UV 样本均显示以淋巴细胞浸润为主,每高倍视野(HPF)超过 10 个细胞(98.2%的荨麻疹,98.8%的 UV),只有 2 例(0.8%)UV 患者以中性粒细胞浸润为主(每 HPF 超过 10 个细胞)。
我们发现,荨麻疹和 UV 均显示以淋巴细胞浸润为主,伴有 RBC 外渗、内皮细胞肿胀和 UV 中的纤维蛋白沉积。此外,与荨麻疹相比,UV 病变中显著的神经周围、血管周围和间质嗜酸性粒细胞浸润是这些细胞在 UV 发病机制中特殊作用的另一个表现。