Kawasaki Disease: Unusual Presentation with Retropharyngeal Involvement.

IF 0.7 Q4 PEDIATRICS Case Reports in Pediatrics Pub Date : 2023-01-01 DOI:10.1155/2023/4913700
Chiara Zeroli, Armela Gorica, Giulia Claire D'Aleo Canova, Monica Caruso, Paolo Castelnuovo, Francesca De Bernardi
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Abstract

Background: Kawasaki disease is an acute febrile generalized vasculitic syndrome of childhood of unknown ethology. The most severe complication may involve the hearth and include acute myocarditis with hearth failure, arrythmia, and coronary artery aneurism. The typical clinical symptoms are fever, conjunctivitis, rash, cervical lymphadenopathy, and mucocutaneous changes, and the diagnosis is made by the clinical criteria. Early use of aspirin and immunoglobuline improves symptoms and prevent heart complications. Case Presentation. A 4-year-old male presented to our attention for multiple unilateral laterocervical lymphadenopathies, odynophagia, and neck stiffness, initially treated with IV antibiotic therapy with partial resolution of symptoms. After four months he made a new ER access for cervicalgia, tonsils asymmetry, trismus, stiff neck, lameness, and phalanx hyperaemia and increase in the size of cervical lymph nodes. Radiology showed increase of lymphnodes dimension and retropharyngeal space asymmetry. The same day heart murmur appeared, so the patient underwent cardiological evaluation that documented dilation of the coronary arteries. This sign made it possible to place the diagnostic suspicion of Kawasaki disease and to start IV immunoglobulins and acetylsalicylic acid administration with prompt response.

Conclusions: Kawasaki disease presents with a range of symptoms which, taken individually, are very common in childhood. One of these symptoms is represented by the swollen of neck lymph nodes. It is only clinical reasoning that leads to the correct diagnosis, and therefore, to the correct setting of the therapy, reducing the risk of complications.

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川崎病:有咽后受累的不寻常表现。
背景:川崎病是一种病因不明的儿童急性发热性全身性血管综合征。最严重的并发症可累及心脏,包括急性心肌炎伴心脏衰竭、心律失常和冠状动脉动脉瘤。临床典型症状为发热、结膜炎、皮疹、颈淋巴肿大、皮肤粘膜改变,根据临床标准诊断。早期使用阿司匹林和免疫球蛋白可改善症状并预防心脏并发症。案例演示。一名4岁男性患者因多发单侧颈侧淋巴结病、吞咽困难和颈部僵硬而引起我们的注意,最初接受静脉抗生素治疗,症状部分缓解。4个月后,他因颈痛、扁桃体不对称、牙关紧闭、颈部僵硬、跛行、指骨充血和颈部淋巴结增大而重新进入急诊室。影像学显示淋巴结肿大,咽后间隙不对称。当天出现心脏杂音,因此患者接受了心脏学评估,记录了冠状动脉扩张。这一征象使诊断怀疑为川崎病成为可能,并开始静脉注射免疫球蛋白和乙酰水杨酸,反应迅速。结论:川崎病表现出一系列症状,单独来看,这些症状在儿童时期非常常见。其中一种症状是颈部淋巴结肿大。只有临床推理才能导致正确的诊断,从而导致正确的治疗方案,减少并发症的风险。
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11.10%
发文量
48
审稿时长
13 weeks
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