Kavasaki综合征临床1例

V. Tkach, M. Voloshynovych, B. Zubyk, L.A. Vitovska, Yu.V. Tsipochka, N. Kozak
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引用次数: 0

摘要

川崎综合征在欧洲很少见。1967年,日本儿科医生川崎富作首次描述了这种相对“年轻”的疾病。这种疾病的病因尚不清楚。大多数科学家倾向于认为,这种疾病是由体内现有的病毒或细菌感染灶引发的,引起炎症和对血液和淋巴管的损害。川崎综合征是一种非传染性疾病,但也有复发病例。38-40°C范围内的高温患者可出现多形态皮疹:红疹、红斑、荨麻疹、丘疹,可模仿麻疹或猩红热。孩子易流泪,易怒,常醒,腹泻,腹痛。皮疹影响四肢和躯干。下肢和上肢肿胀;手掌、脚底和手指的肿胀尤为明显。1、5-2周后,指尖和脚趾出现片状剥落。指间关节肿胀,儿童关节的活跃运动引起疼痛和哭闹。口腔粘膜充血,舌头呈深红色,也诊断为口唇炎。该病有三个阶段:急性期(发病后两周内)、亚急性期(2至4周)和恢复期(1至3个月)。在大多数患者中,颈部淋巴结受到影响,通常触诊到一个淋巴结,直径从1到1.5厘米不等。目前还没有专门的实验室检查来诊断这种综合征。考虑到散发的性质和复杂性的诊断,我们提出了一个3.5岁的男孩川崎综合征的临床病例。该疾病的可能原因是水痘病毒和COVID-19的组合。该综合征的各种症状导致诊断错误,从而影响了初级保健医生的治疗策略。临床表现,并发症,患者途径,复杂的治疗和康复的描述。在我们的报告中,我们提请儿科医生、家庭医生和皮肤科医生注意这样一个事实,即川崎综合征在大流行期间并非罕见疾病,COVID-19与其他病毒和微生物感染的结合导致严重并发症的可能性增加了数倍。及时诊断和合理治疗是预防诊断错误和并发症的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical case of Kavasaki syndrome
Kawasaki syndrome is rare in Europe. This relatively «young» disease was first described by Japanese pediatrician Tomisaku Kawasaki in 1967. The causes of the disease are not clear. Most scientists tend to believe that the disease is triggered by existing foci of infection of viral or bacterial origin in the body, causing inflammation and damage to blood and lymphatic vessels. Kawasaki syndrome is a non­contagious disease, but cases of recurrence have been described.Patients with a high temperature, in the range of 38—40 °C, develop polymorphic rashes: roseola, erythema, urticaria, papules that can mimic measles or scarlet fever. Children are tearful, irritable, often wake up, suffer from diarrhea, abdominal pain. The rash affects the extremities and torso. The lower and upper extremities are swollen; especially pronounced swelling is on the palms, soles and fingers. After 1,5—2 weeks there is a lamellar peeling of the fingertips and toes. The interphalangeal joints are swollen, active movements in children’s joints cause pain and crying as a result. The mucous membranes of the oral cavity are hyperemic, the tongue is deep red (crimson), cheilitis is also diagnosed. There are three phases of the disease: acute — within 2 weeks since the onset, subacute — from 2 to 4 weeks, the recovery phase — from 1 to 3 months. In most patients, the cervical lymph nodes are affected, often one node is palpated ranging in size from 1 to 1.5 cm in diameter. There are no specific laboratory tests to diagnose the syndrome.Considering the sporadic nature and complexity of the diagnosis, we present a clinical case of Kawasaki syndrome in a 3.5­year­old boy. The probable cause of the disease was a combination of chickenpox virus and COVID­19. The variety of symptoms of the syndrome led to diagnostic errors and, accordingly, influenced the tactics of treatment of the primary care physician. Clinical manifestations, complications, route of the patient, complex treatment and rehabilitation are described.In our report, we have focused the attention of pediatricians, family physicians and dermatologists on the fact that Kawasaki syndrome is not a rare disease during the pandemic, and the combination of COVID­19 with other viral and microbial infections led to a multifold increase in the likelihood of serious complications. Timely diagnosis and rational therapy are the prevention of diagnostic errors and complications.
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