Sudden unexpected intrapartum death and left ventricular noncompaction involving the right ventricle

• DOI: 10.1016/j.carpath.2024.107633
• Publication Date: 2024-03-12T08:02:00Z
• Authors: Giulia Ottaviani; Tobia Tomasello; Francesca Boggio; Letterio Runza; Alessandro Del Gobbo; L. Maximilian Buja
• Keywords: Adult; Death, Sudden, Cardiac; Isolated Noncompaction of the Ventricular Myocardium; Pregnancy; Autopsy; Brainstem; Cardiac conduction system; Left ventricular noncompaction involving the right ventricle; Sudden unexpected intrapartum death; Heart Ventricles; Humans; Female; Gestational Age; Autopsy; Stillbirth; Fetal Death

Left ventricular noncompaction (LVNC), involving mainly the right ventricle, is a rare form of congenital heart disorder characterized by a developmental arrest in myocardial compaction, resulting in a spongy appearance of the myocardium, mainly of the right ventricle, rarely detected in fetuses. We report the case of a female fetus with a gestational age of 41+4 weeks who came to our attention for intrapartum sudden unexpected death, resulting in stillbirth. The ventricular walls, particularly the right ventricular wall, appeared thick, hypertrabeculated and spongy, leading to the diagnosis of LVNC involving mainly the right ventricle. The atrioventricular node and His bundle presented areas of fetal dispersion and resorptive degeneration; islands of conduction tissue were detected in the central fibrous body. Arcuate nucleus of the brainstem showed bilateral severe hypoplasia. The right bundle branch was hypoplastic. The final cause of death was an electrical conduction disfunction in an LVNC involving mainly the right ventricle. To the best of our knowledge, the herein described case is the first reported observation of sudden intrapartum death from LVNC involving mainly the right ventricle well documented post-mortem with cardiac conduction and brainstem studies. Our findings confirm the need of an accurate post-mortem examination including the study of the cardiac conduction system on serial section in every case of sudden unexpected fetal death, although there are no universally recognized guidelines.