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태아복수가 출생 후 KT 증후군으로 진단받은 1예Fetal Ascites Proven as Klippel-Trenaunay Syndrome after Birth: A Case Report

Other Titles
Fetal Ascites Proven as Klippel-Trenaunay Syndrome after Birth: A Case Report
Authors
김효진조혜정김은진김석영손동우
Issue Date
Mar-2022
Publisher
대한주산의학회
Keywords
Klippel-Trenaunay syndrome; Ascites; Chylous ascites; Breast feeding; Newborn infant
Citation
Perinatology, v.33, no.1, pp.53 - 57
Journal Title
Perinatology
Volume
33
Number
1
Start Page
53
End Page
57
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/83991
ISSN
2508-4887
Abstract
Fetal ascites may occur for various reasons, and the prognosis depends on the underlying pathology. Fetal chylous ascites is a rare form of fetal ascites that results from the leakage of lymph into the peritoneal cavity. Klippel-Trenaunay syndrome (KTS) is a rare congenital anomaly characterized by vascular malformations of the capillary, venous and lymphatic vessels, unilateral soft and skeletal tissue hypertrophy, usually the lower extremity. We diagnosed a preterm infant with fetal ascites on prenatal ultrasonography, and it was confirmed as chylous ascites after birth. It was also later proven to be associated with KTS as the patient had certain characteristic skin lesions. The chylous ascites resolved with paracentesis and breastfeeding. We report this case along with a review of the relevant literature.
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