Iranian Journal of Pediatrics
Tehran University of Medical Sciences Press
Vol. 21, No. 1, 2011, pp. 113-115
Bioline Code: pe11020
Full paper language: English
Document type: Case Report
Document available free of charge
Iranian Journal of Pediatrics, Vol. 21, No. 1, 2011, pp. 113-115
© Copyright 2010 Iran Journal of Pediatrics.
Placental Chorioangioma as the Cause of Non-Immunologic Hydrops Fetalis; a Case Report|
Duro, Eduardo Alfredo & Moussou, Ines
Chorioangiomas are the most common benign tumors of the placenta originating from primitive angioblastic tissues. It comprises near 1 percent of placental tumors. Clinical manifestations in the newborn are rare and usually associated with tumors greater than 5 cm in diameter and consist of polyhydramnios, fetal anemia, massive edema with pleural effusion, ascites and intrauterine growth retardation. We present a case with large chorioangioma as the cause of non-immunologic hydrops fetalis with a successful outcome.
The patient was a female newborn with history of polyhydramnios, symptoms of congestive heart failure and associated anemia, thrombocytopenia and coagulopathy. The pathophysiology and management of the complications of hydrops fetalis with chorioangioma are discussed
Chorioangioma of the placenta has potentially serious perinatal risks and so the pregnancy needs to have regular surveillance. The chance of developing complications is directly related with the tumor size.
Placental Disease; Tumor; Chorioangioma; Hydrops Fetalis; Anemia; Fetus; Heart Failure
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