Your browser doesn't support javascript.
loading
A Case of Non-Immune Hydrops Fetalis due to Umbilical Venous Malformation and Noonan Syndrome / 대한주산의학회잡지
Korean Journal of Perinatology ; : 300-305, 2013.
Artigo em Coreano | WPRIM | ID: wpr-177249
ABSTRACT
Anomalies of the fetal venous system are rare. Major portion of fetal venous anomalies are malformation of umbilical vein and ductus venosus. Abnormal umbilico-systemic shunt, bypassing the ductus venosus makes direct connection between the high-pressure umbilical system and the low-pressure systemic system. And it makes adverse to the fetal hemodynamics. Fetal hemodynamic distress may induce fetal growth retardation, hepatomegaly, cardiomegaly, hydrops fetalis and fetal death. We report a case of non-immune hydrops fetalis which was associated with abnormal umbilical vein pathway. Our patient had bifurcated umbilical veins. Main branch of umbilical vein was drained directly to the left internal iliac vein and another branch was drained to the portal vein. After birth, extrahepatic shunt through main branch of umbilical vein that bypassed the portal system was persisted and thrombocytopenia was combined due to consumption in thrombus of a dilated anomalous umbilical vein. Later this case was diagnosed as Noonan syndrome with a genetic testing.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Sistema Porta / Veia Porta / Trombocitopenia / Trombose / Veias Umbilicais / Hidropisia Fetal / Testes Genéticos / Cardiomegalia / Parto / Malformações Vasculares Limite: Humanos Idioma: Coreano Revista: Korean Journal of Perinatology Ano de publicação: 2013 Tipo de documento: Artigo

Similares

MEDLINE

...
LILACS

LIS

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Sistema Porta / Veia Porta / Trombocitopenia / Trombose / Veias Umbilicais / Hidropisia Fetal / Testes Genéticos / Cardiomegalia / Parto / Malformações Vasculares Limite: Humanos Idioma: Coreano Revista: Korean Journal of Perinatology Ano de publicação: 2013 Tipo de documento: Artigo