背景:川崎病(KD),也被称为粘膜皮肤淋巴结综合征,是急性的,病因不明的自限性血管炎,主要累及中小动脉,可导致严重的心血管并发症,冠状动脉瘤的发生率为25%.Periton-Sillar脓肿是KD的罕见症状,在早期容易误诊。
方法:一名5岁男孩因3天的发烧来到社区医院,难以张开嘴,和颈部疼痛,最初治疗咽喉感染没有改善。在实验室测试的基础上,颌下和浅表淋巴结的超声和颈部的计算机断层扫描,临床医生诊断为杏仁核周围脓肿和脓毒症,但抗生素治疗后仍未消退.在入学的第五天,这个孩子出现了结膜充血,修剪舌头,肛周充血和脱皮,双脚上稍有僵硬和肿胀。静脉注射免疫球蛋白治疗后,KD的诊断完全缓解。
结论:患有颈部疼痛的儿童,淋巴结肿大,或以气道阻塞为主要表现的静脉广谱抗生素治疗效果不佳。临床医生不应该急于侵入性操作,如颈部穿刺,切口,和引流,当不能解释为颈深间隙感染和阿司匹林联合丙种球蛋白早期治疗时,应警惕KD。
BACKGROUND: Kawasaki disease (KD), also known as mucocutaneous lymph node syndrome, is an acute, self-limiting vasculitis of unknown aetiology that mainly involves the medium and small arteries and can lead to serious cardiovascular complications, with a 25% incidence of coronary artery aneurysms. Periton-Sillar abscesses are a rare symptom of KD and is easily misdiagnosed at its early stages.
METHODS: A 5-year-old boy who presented to a community hospital with a 3-d fever, difficulty in opening his mouth, and neck pain and was originally treated for throat infection without improvement. On the basis of laboratory tests, ultrasound of submandibular and superficial lymph nodes and computed tomography of the neck, the clinician diagnosed the periamygdala abscess and sepsis that did not resolve after antibiotic therapy. On the fifth day of admission, the child developed conjunctival congestion, prune tongue, perianal congestion and desquamation, and slightly stiff and swollen bunions on both feet. A diagnosis of KD was reached with complete remission after intravenous immunoglobulin treatment.
CONCLUSIONS: Children with neck pain, lymph node enlargement, or airway obstruction as the main manifestations are poorly treated with intravenous broad-spectrum antibiotics. Clinicians should not rush invasive operations such as neck puncture, incision, and drainage and should be alert for KD when it cannot be explained by deep neck space infection and early treatment with aspirin combined with gammaglobulin.