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Sudden unexpected intrapartum death and left ventricular noncompaction involving the right ventricle.
Ottaviani, Giulia; Tomasello, Tobia; Boggio, Francesca; Runza, Letterio; Gobbo, Alessandro Del; Buja, L Maximilian.
Affiliation
  • Ottaviani G; Anatomic Pathology, Lino Rossi Research Center, Department of Biomedical, Surgical and Dental Sciences, Università degli Studi di Milano, 20122 Milan, Italy; Department of Pathology and Laboratory Medicine, University of Texas Health Science Center at Houston (UTHealth), McGovern Medical School, Hou
  • Tomasello T; Department of Pathology, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, 20122 Milan, Italy.
  • Boggio F; Department of Pathology, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, 20122 Milan, Italy.
  • Runza L; Department of Pathology, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, 20122 Milan, Italy.
  • Gobbo AD; Department of Pathology, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, 20122 Milan, Italy.
  • Buja LM; Department of Pathology and Laboratory Medicine, University of Texas Health Science Center at Houston (UTHealth), McGovern Medical School, Houston, TX 77030, USA.
Cardiovasc Pathol ; 71: 107633, 2024.
Article in En | MEDLINE | ID: mdl-38485103
ABSTRACT
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stillbirth / Heart Ventricles Limits: Adult / Female / Humans / Pregnancy Language: En Journal: Cardiovasc Pathol Journal subject: ANGIOLOGIA / CARDIOLOGIA / PATOLOGIA Year: 2024 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stillbirth / Heart Ventricles Limits: Adult / Female / Humans / Pregnancy Language: En Journal: Cardiovasc Pathol Journal subject: ANGIOLOGIA / CARDIOLOGIA / PATOLOGIA Year: 2024 Document type: Article Country of publication: