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Case Report
A case of postoperative nasopharyngeal reflux associated with retropharyngeal lymphangioma in newborn infant
Kyo Yeon Koo, Jun Seok Lee, Soon Min Lee, Min Soo Park, Ran Namgung, Kook In Park, Chul Lee, Choon Sik Yoon, Woo Hee Jung, Hong Shik Choi
Clin Exp Pediatr. 2010;53(2):258-261.   Published online February 15, 2010
Lymphangioma is a rare benign congenital tumor of the lymphatic system, which is commonly diagnosed before 2 years of age. In the natronal report, cystic lymphangioma was usually reported as a huge translucent mass located in the head and neck area. It's occurrence in retropharyngeal space with respiratory obstruction and swallowing difficulty in neonate is extremely rare and postoperative nasopharyngeal...
A Case of Retroperitoneal Cystic Lymphangioma
Chang Ho Lee, Jeong Hwa Choi, Eun Ju Han, Jin Gook Kim, Bung Do Nam, Jae Won Back, Mun Kyu Park
Clin Exp Pediatr. 2000;43(1):111-116.   Published online January 15, 2000
Cystic lymphangiomas are comparatively rare, benign tumors of lymphatic system and their histogenesis are uncertain. About 75% of theses lesions are in the neck, 20% are in the axillary region, and 5% are in the mediastinum, retroperitoneal region or groin. But retroperitoneal cysticlymphangiomas are very rare. Retroperitoneal cystic lymphangiomas are usually found incidentally during diagnostic procedures performed for unrelated clinical...
Original Article
A Case of Retroperitoneal Lymphangioma.
Gyu Jin Oh, Jin Hyeon Park, Hee Jung Kwon, In Sil Lee, Kui Won Park, Je Geun Chi
Clin Exp Pediatr. 1990;33(3):422-428.   Published online March 31, 1990
Cystic lymphangioma, or cystic hygroma, is a true, benign, congenital multic-ystic tumor arising from sequestration of embryonic lymphatic tissue. Most often it occurs at birth or early in life, and it was found most commonly in the neck, but rarely in the retroperitoneum and its distribution coincides with that of the primitive lymph sac. We have experienced a case of retroperitoneal cystic lymphangioma in...
Case Report
A Case of Acardius Twin.
Kyung Hyo Kim, Jung Soo Park, Mina Lee, Hye Kyung Lee, Sung Sik Shin, Je G Chi
Clin Exp Pediatr. 1984;27(1):84-88.   Published online January 31, 1984
A case of acardiac twins to a 30 year-old primiparous mother is presented. This case was diagnosed to have this anomaly by ultrasonography at 28 weeks and 33 weeks of gestation. The acardiac monster was delivered as the second twin without any signs of Life. It weighed 2,175 gms and was connected to the placenta by an umbilical cord having...
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