Prenatal diagnosis of noncompaction of the ventricular myocardium: A case report

Authors

  • Alberto Sosa Olavarría Professor of Obstetrics, University of Carabobo, Valencia, Venezuela; Perinatal Diagnosis Unit, Polyclinic Center Valencia, Venezuela. https://orcid.org/0000-0003-4776-7375

DOI:

https://doi.org/10.31403/rpgo.v66i2289

Keywords:

Cardiomyopathy, non-compacted, Isolated noncompaction of the ventricular myocardium, Prenatal diagnosis, Ultrasound

Abstract

"Spongy cardiomyopathy" or noncompaction heart disease is a rare congenital cardiomyopathy of unknown etiology which results from a failure in embryogenesis in the evolutionary process of normal myocardial trabeculation. The characteristic echocardiographic findings of this disease consist of multiple myocardial trabeculations and deep intertrabecular recesses that communicate with the left or right ventricular cavity or both. We present a case of this cardiomyopathy that affects the right ventricle, in a fetus of 31 weeks gestation, whose mother was an asymptomatic carrier of said pathology. Prenatal ultrasound images are presented, including evaluation using the strain (myocardial deformation) technique, emphasizing the importance of the patient’s medical history, possible etiologies and differential diagnosis with other entities.

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Published

2020-12-03

How to Cite

Sosa Olavarría, A. (2020). Prenatal diagnosis of noncompaction of the ventricular myocardium: A case report. The Peruvian Journal of Gynecology and Obstetrics, 66(4). https://doi.org/10.31403/rpgo.v66i2289

Issue

Section

Casos Clínicos

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