CC BY 4.0 · Rev Bras Ginecol Obstet 2018; 40(11): 722-725
DOI: 10.1055/s-0038-1673677
Case Report
Thieme Revinter Publicações Ltda Rio de Janeiro, Brazil

Fetal Noncompaction Cardiomyopathy and Histologic Diagnosis of Spongy Myocardium: Case Report and Review of the Literature

Luigi Nappi
1   Department of Medical and Surgical Sciences, Institute of Obstetrics and Gynecology, Università di Foggia, Foggia, Italy
,
Lorenzo Vasciaveo
1   Department of Medical and Surgical Sciences, Institute of Obstetrics and Gynecology, Università di Foggia, Foggia, Italy
,
Felice Sorrentino
1   Department of Medical and Surgical Sciences, Institute of Obstetrics and Gynecology, Università di Foggia, Foggia, Italy
,
Gennaro Scutiero
2   Section of Obstetrics and Gynecology, Department of Morphology, Surgery and Experimental Medicine, Università degli Studi di Ferrara, Ferrara, Italy
,
Piergiorgio Iannone
2   Section of Obstetrics and Gynecology, Department of Morphology, Surgery and Experimental Medicine, Università degli Studi di Ferrara, Ferrara, Italy
,
Pantaleo Greco
2   Section of Obstetrics and Gynecology, Department of Morphology, Surgery and Experimental Medicine, Università degli Studi di Ferrara, Ferrara, Italy
› Author Affiliations
Further Information

Publication History

21 June 2018

09 August 2018

Publication Date:
11 October 2018 (online)

Abstract

Noncompaction cardiomyopathy (NCCM) and left ventricular noncompaction (LVNC), in their isolated form, are rare cardiomyopathies. They are characterized by a thickened myocardium due to the presence of deep trabeculae recesses, and to thick trabeculae. This condition is associated with a variable clinical phenotype including heart failure, thromboembolism, and sudden death. We report a case of LVNC at 26 weeks and 4 days of gestation revised on the basis of what is currently reported in the literature. A review of the literature was performed to better describe this rare condition. Left ventricular noncompaction is a rare fetal condition and it should be suspected in case of cardiomyopathy.

 
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