Chircor Lidia, Mehedinţi Rodica, Hîncu Mihaela
Department of Normal and Pathological Morphology, "Ovidius" University, Constanta, Romania.
Rom J Morphol Embryol. 2009;50(4):645-9.
Omphalocele and gastroschisis are recognized as congenital malformations with a high mortality. Only 60% of children with such malformations survive until the end of the first year of age. It has been suggested that omphalocele and gastroschisis are associated with other congenital malformations, concerning the bones, the heart and the kidney. The aim of the present study is to determine the risk factors in 12 omphalocele and four gastroschisis cases diagnosed and surveyed in the last four years (November 2003-November 2007) at the Emergency County Hospital of Constanta. In 10 of the 16 cases of the studied group, the subjects resulted from spontaneous premature births. None of the cases in the studied group received the maximum APGAR score, values varying between 6 and 9. The average birth weight in the studied group is 2100 g, with values between 950 g and 2900 g. Maternal age is between 15-21-year-old. Average maternal age in cases of second-degree gastroschisis is 6.5 years younger than the witness population and in case of first degree is 5.8 years younger. 87.5% of children's mothers in studied group are first time pregnant, first time gestant. The mother's socio-economic status may be a risk factor on the occurrence of omphalocele and gastroschisis. 81.25% of children's mother in the studied group have no own income and half are single (mono-parental families). None of the studied cases had a history of congenitally malformed siblings, but half of the cases in the studied group associate congenital malformations of gastro-intestinal tract, locomotor system, kidneys and/or heart. The abdominal wall defect existing in gastroschisis is accompanied by the delay of the intestinal loops differentiation. In all cases of gastroschisis in the studied group, the thin intestine caliber is higher or equal to the one of the thick intestine, the intestinal loops remained outside the abdominal cavity have an aspect characteristic to the fifth month of fetal life.
脐膨出和腹裂被认为是死亡率很高的先天性畸形。患有此类畸形的儿童只有60%能存活到一岁末。有人提出,脐膨出和腹裂与骨骼、心脏和肾脏等其他先天性畸形有关。本研究的目的是确定过去四年(2003年11月至2007年11月)在康斯坦察县急诊医院诊断和调查的12例脐膨出和4例腹裂病例中的危险因素。在研究组的16例病例中,有10例是自发早产。研究组中没有一例获得最高阿氏评分,评分在6至9分之间。研究组的平均出生体重为2100克,体重在950克至2900克之间。产妇年龄在15至21岁之间。二度腹裂病例的平均产妇年龄比对照人群小6.5岁,一度腹裂病例的平均产妇年龄比对照人群小5.8岁。研究组中87.5%的儿童母亲是初孕、初产。母亲的社会经济地位可能是脐膨出和腹裂发生的一个危险因素。研究组中81.25%的儿童母亲没有自己的收入,一半是单身(单亲家庭)。研究的病例中没有先天性畸形兄弟姐妹的病史,但研究组中有一半病例伴有胃肠道、运动系统、肾脏和/或心脏的先天性畸形。腹裂中存在的腹壁缺损伴有肠袢分化延迟。在研究组的所有腹裂病例中,细肠管径大于或等于粗肠管径,留在腹腔外的肠袢具有胎儿生命第五个月的特征外观。