Autopsy report of a sudden infant death that was strongly suspicious of Kawasaki disease

Author:

Yokouchi Yuki1ORCID,Asakawa Nanae1,Iwase Hirotaro2,Nasu Takeshi3,Takahashi Kei1

Affiliation:

1. Department of Surgical Pathology Toho University Ohashi Medical Center Tokyo Japan

2. Department of Legal Medicine, Graduate School of Medicine Chiba University Chiba Japan

3. Nasu Pediatrics Chiba Japan

Abstract

AbstractWe 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.

Publisher

Wiley

Reference19 articles.

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