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Case Report
Copyright ©The Author(s) 2025. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Clin Cases. Dec 26, 2025; 13(36): 114472
Published online Dec 26, 2025. doi: 10.12998/wjcc.v13.i36.114472
Cardiac arrest as initial presentation of Kawasaki disease with giant coronary aneurysms: A case report and review of literature
Dat Minh-Tan Truong, Liem Thanh Bui, Tam Khiet Nguyen, Hieu Trong Pham, Bao Quoc Vo, Thanh Tat Nguyen
Dat Minh-Tan Truong, Liem Thanh Bui, Hieu Trong Pham, Bao Quoc Vo, Department of Intensive Care Unit, Children’s Hospital 2, Ho Chi Minh City 700000, Viet Nam
Liem Thanh Bui, Department of Pediatrics, University of Medicine and Pharmacy, Ho Chi Minh City 700000, Viet Nam
Tam Khiet Nguyen, Department of Cardiology, Children’s Hospital 2, Ho Chi Minh City 700000, Viet Nam
Thanh Tat Nguyen, Department of Infectious Diseases, Children’s Hospital 2, Ho Chi Minh City 700000, Viet Nam
Co-first authors: Dat Minh-Tan Truong and Liem Thanh Bui.
Author contributions: Truong DMT and Bui LT contributed equally to this manuscript and are co-first authors. Truong DMT, Bui LT, Vo BQ, and Nguyen TT contributed to the conceptualization; Truong DMT and Bui LT contributed to the data curation and funding acquisition; Nguyen TT was involved in the formal analysis; Truong DMT, Pham HT, and Nguyen TT participated in the investigation; Truong DMT, Bui LT, and Pham HT contributed to the methodology of this manuscript; Truong DMT, Bui LT, Pham HT, and Nguyen TT wrote the original draft; Truong DMT, Bui LT, Vo BQ, and Nguyen TT contributed to the critical revision of the final manuscript. All authors have contributed to and approved the final manuscript.
Informed consent statement: Informed written consent was obtained from the patient for publication of this report and any accompanying images.
Conflict-of-interest statement: All the authors report no relevant conflicts of interest for this article.
CARE Checklist (2016) statement: The authors have read the CARE Checklist (2016), and the manuscript was prepared and revised according to the CARE Checklist (2016).
Open Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Thanh Tat Nguyen, MD, PhD, Senior Researcher, Department of Infectious Diseases, Children’s Hospital 2, Ly Tu Trong, Ho Chi Minh City 700000, Viet Nam. thanhhonor@gmail.com
Received: September 22, 2025
Revised: October 20, 2025
Accepted: December 11, 2025
Published online: December 26, 2025
Processing time: 96 Days and 16 Hours
Abstract
BACKGROUND

Kawasaki disease (KD) is an acute systemic vasculitis in young children that may cause coronary aneurysms, thrombosis, myocardial infarction, and sudden death if diagnosis is delayed.

CASE SUMMARY

We report a 19-month-old male patient who presented after 25 days of progressive illness culminating in sudden cardiac arrest. Initial episodes of fever, cough, and rash were misdiagnosed as viral infection and pneumonia, delaying recognition. On admission following prolonged resuscitation, he was comatose with severe metabolic acidosis, multiorgan dysfunction, and periungual desquamation. Echocardiography demonstrated giant bilateral coronary aneurysms with right coronary artery thrombosis, consistent with KD complicated by myocardial infarction. Management included mechanical ventilation, high-dose vasopressors, intravenous immunoglobulin, corticosteroids, anticoagulation, and antibiotics. Continuous renal replacement therapy, targeted temperature management, and therapeutic plasma exchange were employed to control cytokine storm and organ failure. The patient stabilized hemodynamically, was extubated by day 12, and subsequently transferred for cardiology care. Follow-up imaging confirmed persistent aneurysms without thrombosis, preserved cardiac function, and favorable neurological recovery.

CONCLUSION

This case underscores the challenges of recognizing atypical KD and highlights the importance of early suspicion, rapid resuscitation, and multimodal therapies, including Continuous renal replacement therapy and therapeutic plasma exchange, in improving survival and neurological outcomes.

Keywords: Kawasaki disease; Cardiac arrest; Coronary artery aneurysm; Continuous renal replacement therapy; Therapeutic plasma exchange; Viet Nam; Case report

Core Tip: Kawasaki disease (KD) is a childhood illness that can damage the heart if not recognized early. We describe a 19-month-old boy who developed fever, cough, and rash for almost a month, but was repeatedly treated as having infections. He suddenly went into cardiac arrest and was found to have severe heart vessel damage with clots from undiagnosed KD. He required prolonged resuscitation, advanced life support, and multiple treatments including cooling therapy, combined interventions of continuous renal replacement and plasma exchange. Remarkably, he recovered with good heart and brain function, showing the importance of early recognition and aggressive care in severe KD.