Mirror syndrome with noncompaction cardiomyopathy in the mother and fetus. Case report

• Published in: Revista colombiana de obstetricia y ginecología Vol. 72; no. 3; pp. 298 - 306
• Main Authors: Velásquez-Penagos, Jesús Arnulfo, Flórez-Ríos, Ana María, Muñoz-Ortiz, Edison, Gándara-Ricardo, Jairo Alfonso, Flórez-Muñoz, Juan Pablo, Holguín-González, Erika
• Format: Journal Article
• Language: English; Spanish
• Published: 30.09.2021
• ISSN: 2463-0225
• DOI: 10.18597/rcog.3659

ObjectiveTo report the case of a pregnant woman with mirror syndrome associated with non-compaction cardiomyopathy in the mother and the fetus, in which antenatal medical treatment provided to the mother resulted in a favorable perinatal maternal outcome. Case presentationA 16-year old primigravida with 33 weeks of gestation referred from a Level I institution to a private Level IV center in Medellín, Colombia, because of a finding of fetal hydrops on obstetric ultrasound. During hospitalization, the patient showed clinical and ultrasonographic signs of heart failure (dyspnea, edema and hypoxemia), with the diagnosis of hydrops fetalis (mirror syndrome) also confirmed. Diuretic treatment with furosemide was initiated in the mother, with subsequent improvement of the maternal condition as well as of the fetal edema. During the subacute postpartum period in the hospital, the presence of non-compaction cardiomyopathy was confirmed on cardiac nuclear magnetic resonance imaging in both the mother and the newborn. After discharge in adequated condition, they were included in the cardiovascular follow-up program for heart failure and congenital heart disease, respectively. ConclusionA case of mirror syndrome associated with maternal and fetal non-compaction cardiomyopathy is presented. There is a limited number of reports on mirror syndrome due to cardiac anomalies (maternal and fetal), with weak treatment descriptions, pointing to the need for research in this area. It would be important to consider the diagnosis of non-compaction cardiomyopathy in fetuses with hydrops unrelated to isoimmunization or cardiac dysfunction, and approach these cases from a multi-disciplinary perspective.