Department of Surgical Pathology, Toho University Ohashi Medical Center, Tokyo, Japan.
Department of Legal Medicine, Graduate School of Medicine, Chiba University, Chiba, Japan.
Pathol Int. 2024 Jul;74(7):408-414. doi: 10.1111/pin.13437. Epub 2024 May 15.
We conducted an autopsy on a 3-month-old boy in whom Kawasaki disease (KD) was strongly suspected based on the autopsy findings. The infant had a fever and was brought to a nearby clinic, where he was prescribed antipyretics and kept under observation. However, 15 days after onset of the fever, he suddenly died in bed. He exhibited no obvious redness of the lips, tongue, or conjunctiva. Membranous desquamation was present on his distal fingers. Vasculitis was observed in the coronary arteries, renal artery, splenic artery, and pulmonary vein. In addition, coronary artery aneurysms were present in the right coronary artery and left anterior descending artery. Thrombotic occlusion was observed in one aneurysm in the right coronary artery, resulting in acute myocardial infarction. The coronary artery wall showed infiltration of numerous macrophages and neutrophils. This case was classified as incomplete KD because the coronary artery aneurysm could not be demonstrated before death and was only recognized at autopsy. Pathologists and forensic scientists need to be aware that there are cases in which KD goes undiagnosed and untreated, leading to coronary artery aneurysm formation and sudden death.
我们对一名 3 个月大的男婴进行了尸检,该男婴根据尸检结果强烈怀疑患有川崎病(KD)。婴儿发烧,并被带到附近的诊所,在那里他被开了退烧药并进行观察。然而,发烧 15 天后,他突然在床上死亡。他的嘴唇、舌头或结膜没有明显的发红。他的远端手指有膜状脱皮。在冠状动脉、肾动脉、脾动脉和肺静脉中观察到血管炎。此外,右冠状动脉和左前降支存在冠状动脉瘤。在右冠状动脉的一个动脉瘤中观察到血栓闭塞,导致急性心肌梗死。冠状动脉壁有大量巨噬细胞和中性粒细胞浸润。本例被归类为不完全性 KD,因为在死亡前不能显示冠状动脉瘤,只能在尸检时发现。病理学家和法医学家需要意识到,有些川崎病病例未被诊断和治疗,导致冠状动脉瘤形成和突然死亡。