COVID-19 后的 Deverji 病:病例报告

O. Y. Olisova, Natalya P. Teplyuk, Daria M. Martynenko, Ekaterina R. Dunaeva, E. Grekova
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引用次数: 0

摘要

德弗吉氏病是一种罕见的特发性皮肤病,以角化障碍为特征,表现为毛囊角化过度、橙红色脱皮斑、掌跖角化症,并可能发展为红皮病。这种皮肤病的发病机制尚不清楚。可能的诱发因素包括创伤、紫外线辐射、服用某些药物、自身免疫性疾病和肿瘤疾病、细菌或病毒感染、接种疫苗等。家族性病例的出现是由于 CARD14 基因发生了突变。该病的诊断基于特征性的临床症状。组织学检查没有明显的特征;但需要进行活组织检查,以便与其他丘疹鳞屑性皮肤病进行鉴别诊断。由于尚未对该病的发病机制进行充分研究,因此治疗德韦吉氏病仍是一项艰巨的任务。本文描述了一例德弗吉病的临床病例,患者是一名 64 岁的女性,曾两次感染 COVID-19。她因面部、躯干、上肢和下肢出现皮疹并伴有剧烈瘙痒而被塞切诺夫大学皮肤病与维纳学系收治。由于没有任何明显的临床和组织学变化、皮肤瘙痒和抗药性,因此很难做出诊断。在出现特征性临床症状(掌跖角化症、鲑鱼色皮疹伴有健康皮肤岛)以及反复组织学检查结果(正角化区和副角化区交替出现;颗粒层不均匀;基底细胞空泡化;宽窄不均的棘层溶解线;真皮-表皮交界处松动;血管周围淋巴-巨噬细胞小浸润)后,德韦吉氏病被确诊。使用标准疗法(全身糖皮质激素疗法、甲氨蝶呤、局部疗法)没有任何效果,因此决定开始使用奈达单抗。注射 5 次后,首次取得了积极效果,皮疹颜色变浅,数量减少,掌跖角化消退,患者的精神情绪得到改善。11 次注射后,病情几乎完全缓解,治疗一直持续到所有症状完全消失。文章对德韦吉病的发病机制、临床表现和治疗方法进行了文献综述。所描述的临床病例是世界上第五例感染 COVID-19 后出现 Deverji 病的病例,也是第一例成功使用 IL-17 抑制剂 netakimab 治疗该病的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Deverji's disease after COVID-19: Case report
Deverji's disease is a rare idiopathic skin disease characterized by keratinization disorder and manifested in follicular hyperkeratosis, orange-red peeling plaques, palmar-plantar keratodermia with the possible development of erythroderma. The etiopathogenesis of this dermatosis is still unknown. There are such possible trigger factors as traumatization, ultraviolet radiation, taking certain medications, autoimmune and oncological diseases, bacterial or viral infection, vaccination. The presence of familial cases is due to a mutation in the CARD14 gene. Diagnosis of the disease is based on characteristic clinical symptoms. The histological picture has no pathognomonic features; however, a biopsy is necessary for differential diagnosis with other papulosquamous dermatoses. Treatment of Deverji's disease remains a difficult task, since the disease pathogenesis has not been fully studied. The article describes a clinical case of Deverji's disease manifestation in a 64-year-old woman who had suffered COVID-19 infection twice. She was admitted to the Department of Dermatology and Venerology (Sechenov University) with complaints of skin rashes on her face, trunk, upper and lower extremities, accompanied by severe itching. The absence of any distinctive clinical and histological changes, the torpidity of the skin process and resistance to the therapy made it difficult to make a diagnosis. After the emergence of characteristic clinical symptoms (palmar-plantar keratodermia, salmon-tinged rashes with islands of healthy skin), as well as the results of repeated histological examination (alternating areas of ortho- and parakeratosis; uneven granular layer; vacuolization of basal cells; uneven broad acantholytic strands; loosened dermo-epidermal junction; small perivascular lymph-macrophage infiltrates) Deverji's disease was diagnosed. The use of standard therapies (systemic glucocorticosteroid therapy, methotrexate, topical therapy) did not give any results, and therefore it was decided to initiate the netakimab. After 5 injections, the first positive results were obtained in the form of the color paling and a decrease in the number of rashes, palmar-plantar keratodermia regression and improvement of the patient psychoemotional state. After 11 injections, almost complete remission was achieved, and treatment was continued until all symptoms disappeared completely. The article provides a literature review of the etiopathogenesis, clinical manifestations and treatment methods of Deverji's disease. The described clinical case is the fifth example in the world of the Deverji's disease manifestation after a COVID-19 infection, and is also the first case of the IL-17 inhibitor netakimab successful use for the disease treatment.
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