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[Nonimmune hydrops fetalis associated with congenital small bowel atresia--a case study].

Authors :
Pietryga M
Murlewska J
Pietrzycka D
Becela P
Brazert J
Gadzinowski J
Jankowski A
Source :
Ginekologia polska [Ginekol Pol] 2011 Sep; Vol. 82 (9), pp. 709-14.
Publication Year :
2011

Abstract

Nonimmune hydrops fetalis is observed with the frequency of 1:3000 cases diagnosed pre- and postnatally. In the following paper the authors analyzed the course of pregnancy complicated by fetal ascites and polyhydramnios with the appearance of colonic ileus and they presented the postnatal condition of the baby The preliminary diagnosis was confirmed after birth and the newborn was operated in the second day of his life. The congenital small bowel atresia was qualified as a III B type (Grossfeld qualification), which is called the "pagoda" syndrome [3]. The colonic atresia is located then around the superior mesenteric vessels, which leads to colonic necrosis (Figure 1).

Details

Language :
Polish
ISSN :
0017-0011
Volume :
82
Issue :
9
Database :
MEDLINE
Journal :
Ginekologia polska
Publication Type :
Academic Journal
Accession number :
22379934