Department of Pathology, Hospital Infantil Universitario Niño Jesús, Madrid, Spain.
Department of Pathology, Hospital Universitario Fundación Jiménez Díaz, Madrid, Spain.
Br J Dermatol. 2020 Oct;183(4):729-737. doi: 10.1111/bjd.19327. Epub 2020 Aug 5.
Chilblains ('COVID toes') are being seen with increasing frequency in children and young adults during the COVID-19 pandemic. Detailed histopathological descriptions of COVID-19 chilblains have not been reported, and causality of SARS-CoV-2 has not yet been established.
To describe the histopathological features of COVID-19 chilblains and to explore the presence of SARS-CoV-2 in the tissue.
We examined skin biopsies from seven paediatric patients presenting with chilblains during the COVID-19 pandemic. Immunohistochemistry for SARS-CoV-2 was performed in all cases and electron microscopy in one.
Histopathology showed variable degrees of lymphocytic vasculitis ranging from endothelial swelling and endotheliitis to fibrinoid necrosis and thrombosis. Purpura, superficial and deep perivascular lymphocytic inflammation with perieccrine accentuation, oedema, and mild vacuolar interface damage were also seen. SARS-CoV-2 immunohistochemistry was positive in endothelial cells and epithelial cells of eccrine glands. Coronavirus particles were found in the cytoplasm of endothelial cells on electron microscopy.
Although the clinical and histopathological features were similar to other forms of chilblains, the presence of viral particles in the endothelium and the histological evidence of vascular damage support a causal relation of the lesions with SARS-CoV-2. Endothelial damage induced by the virus could be the key mechanism in the pathogenesis of COVID-19 chilblains and perhaps also in a group of patients severely affected by COVID-19 presenting with features of microangiopathic damage. What is already known about this topic? Despite the high number of cases of chilblains seen during the COVID-19 pandemic, a definite causative role for SARS-CoV-2 has not yet been proven. Different pathogenetic hypotheses have been proposed, including coagulation anomalies, interferon release and external factors. What does this study add? The demonstration of SARS-CoV-2 in endothelial cells of skin biopsies by immunohistochemistry and electron microscopy confirms that these lesions are part of the spectrum of COVID-19. Virus-induced vascular damage and secondary ischaemia could explain the pathophysiology of COVID-19 chilblains. Our findings support the hypothesis that widespread endothelial infection by SARS-CoV-2 could have a pathogenetic role in the severe forms of COVID-19. Linked Comment: Wetter. Br J Dermatol 2020; 183:611.
在 COVID-19 大流行期间,儿童和青少年中越来越多地出现冻疮(“COVID 脚趾”)。尚未详细描述 COVID-19 冻疮的组织病理学特征,也尚未确定 SARS-CoV-2 的因果关系。
描述 COVID-19 冻疮的组织病理学特征,并探讨组织中是否存在 SARS-CoV-2。
我们检查了在 COVID-19 大流行期间出现冻疮的 7 名儿科患者的皮肤活检。所有病例均进行 SARS-CoV-2 的免疫组织化学检查,1 例进行电子显微镜检查。
组织病理学显示程度不同的淋巴细胞性血管炎,从内皮肿胀和内皮细胞炎到纤维蛋白样坏死和血栓形成。还可见瘀点、浅表和深在血管周围淋巴细胞性炎症伴毛囊周围加重、水肿和轻度空泡界面损伤。SARS-CoV-2 免疫组织化学染色在血管内皮细胞和小汗腺上皮细胞中呈阳性。电子显微镜下在血管内皮细胞的细胞质中发现冠状病毒颗粒。
尽管临床和组织病理学特征与其他形式的冻疮相似,但内皮细胞中存在病毒颗粒以及血管损伤的组织学证据支持这些病变与 SARS-CoV-2 之间存在因果关系。病毒引起的内皮损伤可能是 COVID-19 冻疮发病机制的关键机制,也可能是 COVID-19 严重患者中出现微血管损伤特征的一个患者群体的发病机制。
关于这个话题已经知道了什么?尽管在 COVID-19 大流行期间出现了大量的冻疮病例,但尚未明确证明 SARS-CoV-2 的致病作用。已经提出了不同的发病机制假说,包括凝血异常、干扰素释放和外部因素。
本研究增加了什么?免疫组织化学和电子显微镜检查显示 SARS-CoV-2 在皮肤活检的内皮细胞中,证实这些病变是 COVID-19 谱的一部分。病毒引起的血管损伤和继发性缺血可能解释了 COVID-19 冻疮的病理生理学。我们的研究结果支持这样一种假说,即 SARS-CoV-2 广泛感染内皮细胞可能在 COVID-19 的严重形式中具有致病作用。
Wetter. Br J Dermatol 2020; 183:611.