Warning: fopen(/home/virtual/pediatrics/journal/upload/ip_log/ip_log_2024-03.txt) [function.fopen]: failed to open stream: Permission denied in /home/virtual/pediatrics/journal/ip_info/view_data.php on line 82

Warning: fwrite(): supplied argument is not a valid stream resource in /home/virtual/pediatrics/journal/ip_info/view_data.php on line 83
A Case of Omphalocele Associated with Multiple Congenital Anomalies.

Journal of the Korean Pediatric Society 1983;26(1):66-70.
Published online January 31, 1983.
A Case of Omphalocele Associated with Multiple Congenital Anomalies.
Yoon Ja Kim1, Soo Kyung Jeong1, Nam Ji Cho1, Jae Keum Ji2
1Department of Pediatrics,National Seoul Hospital, Seoul, Korea
2Department of Pathology,College of Medicine,Seoul National University
다발성 선천성 기형을 동반한 제대탈출증 1례
김윤자1, 정수경1, 조남지1, 지제근2
1국립서울병원 소아과
2서울대학교 의과대학 병리학교실
Abstract
A omphalocele associated with multiple congenital anomalies is extremely rare congenital malformation. We experienced a ruptured large omphalocele of short duration associated with multiple congenital anomalies such as patent omphalomesenteric duct, cleft palate and lip, postaxial polydactylia with dystrophic nails on both hands and leftfoot, adrenal heterotophia in left peritesticular region, pancreatic heterotophia in perisplenic lymphnode, nodular excrescene of spleen, and cystic lymphangioma involving thyroid. A brief case history with autopsy finding and review of literatures were presented.
Key Words: Omphalocele, Multiple congenital anomalies.


METRICS Graph View
  • 670 View
  • 1 Download