Please use this identifier to cite or link to this item: http://imsear.hellis.org/handle/123456789/72690
Title: Diffuse multifocal chorangiomatosis of the placenta with multiple intestinal stenosis of the fetus: combination of rare causes for nonimmune hydrops fetalis.
Authors: Chopra, Anita
Iyer, Venkateswaran K
Thapar, Rajeev
Singh, Neeta
Issue Date: 23-Oct-2006
Citation: Chopra A, Iyer VK, Thapar R, Singh N. Diffuse multifocal chorangiomatosis of the placenta with multiple intestinal stenosis of the fetus: combination of rare causes for nonimmune hydrops fetalis. Indian Journal of Pathology & Microbiology. 2006 Oct; 49(4): 600-2
Abstract: Non-immune causes of hydrops fetalis are rare but frequently fatal. Identification of the cause for hydrops fetalis is essential to institute therapy. Chorangiomatosis and intestinal stenosis have not been previously reported as aetiological factors for the development of hydrops. We report a fetus born with hydrops associated with both of these conditions. A 1575 gms preterm neonate was born to a multigravida at 31 weeks of gestation. Emergency caesarean section was performed after detection of hydrops by prenatal ultrasonography. Baby had generalized edema at birth and died after 3 days due to progressive heart failure. At autopsy there was generalized edema and effusions. There were multiple stenotic segments in the intestine. Placenta showed numerous chorangiomas varying from 0.2 to 3 cm in diameter, hence diagnosed as diffuse multifocal chorangiomatosis. Examination of the placenta at neonatal autopsy is an essential part of assessment for hydrops fetalis. Chorangiomatosis is a rare and under reported condition which can cause prematurity, intrauterine growth retardation, pre-eclampsia and rarely hydrops fetalis.
URI: http://imsear.hellis.org/handle/123456789/72690
Appears in Collections:Indian Journal of Pathology & Microbiology

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