SciELO - Scientific Electronic Library Online

 
vol.72 número3Prenatal ultrasound diagnostic approach to Omenn syndrome: case reportRevisiting the indication for prophylactic contralateral mastectomy in patients with Li-Fraumeni syndrome and breast cáncer. Case report índice de autoresíndice de assuntospesquisa de artigos
Home Pagelista alfabética de periódicos  

Serviços Personalizados

Journal

Artigo

Indicadores

Links relacionados

  • Em processo de indexaçãoCitado por Google
  • Não possue artigos similaresSimilares em SciELO
  • Em processo de indexaçãoSimilares em Google

Compartilhar


Revista Colombiana de Obstetricia y Ginecología

versão impressa ISSN 0034-7434versão On-line ISSN 2463-0225

Resumo

VELASQUEZ-PENAGOS, Jesús Arnulfo et al. Mirror syndrome with noncompaction cardiomyopathy in the mother and fetus. Case report. Rev Colomb Obstet Ginecol [online]. 2021, vol.72, n.3, pp.298-306.  Epub 30-Set-2021. ISSN 0034-7434.  https://doi.org/10.18597/rcog.3659.

Objective:

To report the case of a pregnant woman with mirror syndrome associated with noncompaction cardiomyopathy in the mother and the fetus, in which antenatal medical treatment provided to the mother resulted in a favorable perinatal maternal outcome.

Case presentation:

A 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.

Conclusion:

A 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 multidisciplinary perspective.

Palavras-chave : Hydrops fetalis; cardiomyopathies; placental diseases; isolated noncompaction of the ventricular myocardium.

        · resumo em Espanhol     · texto em Espanhol     · Espanhol ( pdf )