Nozaki Taiki, Morita Yuka, Hasegawa Daisuke, Makidono Akari, Yoshimoto Yuri, Starkey Jay, Kusakawa Isao, Manabe Atsushi, Saida Yukihisa
Department of Radiology, St Luke's International Hospital, Tokyo, Japan.
Department of Pediatrics, St Luke's International Hospital, Tokyo, Japan.
Pediatr Int. 2016 Nov;58(11):1146-1152. doi: 10.1111/ped.13017. Epub 2016 Jul 27.
Differentiating Kawasaki disease (KD) from cervical lymphadenitis (CL) is clinically difficult but essential given that treatment and outcome differ significantly. Research on differentiation between KD and CL using ultrasound (US) and computed tomography (CT) is limited. The purpose of this study was to identify cervical US and CT findings that may differentiate KD from CL.
We retrospectively reviewed cervical US of 25 KD patients and 25 CL patients, and CT of 14 KD patients, and 14 CL patients. Two radiologists analyzed specific imaging features on US (lymph node size, shape, echogenicity, margins, laterality, necrosis, and presence of normal hilum) and on CT (size and location of enlarged nodes, laterality, perinodal infiltration, and retropharyngeal edema).
On US, patients with KD more frequently had lymph nodes with a "cluster of grapes" appearance (KD vs CL: 64% vs 32%, P < 0.05) and less frequently had poorly circumscribed margins (0% vs 36%, P < 0.01), necrosis (0% vs 32%, P < 0.01), or non-visualization of the hilum (4% vs 36%, P < 0.01). On CT, KD patients more frequently had retropharyngeal edema (100% vs 29%, P < 0.001) and less frequently had level 4 lymphadenopathy (14% vs 79%, P < 0.01) than CL patients.
Ultrasound is mainly useful for excluding purulent lymphadenopathy while CT is a useful diagnostic tool for differentiating KD from CL, especially in patients with incomplete KD, who present with prominent cervical lymphadenopathy and other equivocal principal findings.
鉴于川崎病(KD)和颈淋巴结炎(CL)的治疗方法和预后差异显著,临床上区分二者很困难但至关重要。利用超声(US)和计算机断层扫描(CT)鉴别KD和CL的研究有限。本研究的目的是确定可能有助于区分KD和CL的颈部超声及CT表现。
我们回顾性分析了25例KD患者和25例CL患者的颈部超声,以及14例KD患者和14例CL患者的CT。两名放射科医生分析了超声上的特定影像特征(淋巴结大小、形状、回声、边界、侧别、坏死及正常淋巴结门的存在情况)和CT上的特定影像特征(肿大淋巴结的大小和位置、侧别、淋巴结周围浸润及咽后水肿)。
在超声检查中,KD患者的淋巴结更常表现为“葡萄串”样外观(KD与CL:64% 对32%,P < 0.05),边界不清(0% 对36%,P < 0.01)、坏死(0% 对32%,P < 0.01)或淋巴结门不可见(4% 对36%,P < 0.01)的情况较少见。在CT检查中,与CL患者相比,KD患者更常出现咽后水肿(100% 对29%,P < 0.001),而4区淋巴结肿大的情况较少见(14% 对79%,P < 0.01)。
超声主要有助于排除化脓性淋巴结病,而CT是鉴别KD和CL的有用诊断工具,尤其对于不完全KD患者,这类患者表现为明显的颈部淋巴结肿大及其他不明确的主要表现。