中华围产医学杂志
中華圍產醫學雜誌
중화위산의학잡지
CHINESE JOURNAL OF PERINATAL MEDICINE
2009年
6期
413-417
,共5页
林胜谋%方群%王晨虹%陈健生%张铨富%陈筠虹%陈涌珍
林勝謀%方群%王晨虹%陳健生%張銓富%陳筠虹%陳湧珍
림성모%방군%왕신홍%진건생%장전부%진균홍%진용진
胎儿疾病%腹水%产前诊断%腹膜炎%预后
胎兒疾病%腹水%產前診斷%腹膜炎%預後
태인질병%복수%산전진단%복막염%예후
Fetal diseases%Ascites%Prenatal diagnosis%Peritonitis%Prognosis
目的 探讨胎儿腹水的病因、诊断和预后.方法 对79例超声诊断为单胎胎儿腹水的产前诊断结果及妊娠结局进行回顾性分析.结果 79例中,超声提示56例(70.9%)为胎儿水肿综合征表现,23例(29.1%)为单纯性腹水.56例胎儿水肿综合征中29例(51.8%)伴心脏扩大.病因诊断显示79例中,30例为α-重型地中海贫血,9例宫内感染,3例母胎Rh血型不合,Turner综合征和13一三体各1例,胎儿脏器畸形引起的腹水19例,16例病因不明,病因的诊断率79.7%.随访中64例孕妇选择终止妊娠(5例胎死宫内),13例足月分娩(10例健存,包括7例胎粪性腹膜炎和3例特发性腹水),2例失访.结论 胎儿腹水病因复杂,α-重型地中海贫血、胎儿脏器结构畸形和宫内感染为主要病因.建议通过系统方案进行产前诊断并对预后作出评估.
目的 探討胎兒腹水的病因、診斷和預後.方法 對79例超聲診斷為單胎胎兒腹水的產前診斷結果及妊娠結跼進行迴顧性分析.結果 79例中,超聲提示56例(70.9%)為胎兒水腫綜閤徵錶現,23例(29.1%)為單純性腹水.56例胎兒水腫綜閤徵中29例(51.8%)伴心髒擴大.病因診斷顯示79例中,30例為α-重型地中海貧血,9例宮內感染,3例母胎Rh血型不閤,Turner綜閤徵和13一三體各1例,胎兒髒器畸形引起的腹水19例,16例病因不明,病因的診斷率79.7%.隨訪中64例孕婦選擇終止妊娠(5例胎死宮內),13例足月分娩(10例健存,包括7例胎糞性腹膜炎和3例特髮性腹水),2例失訪.結論 胎兒腹水病因複雜,α-重型地中海貧血、胎兒髒器結構畸形和宮內感染為主要病因.建議通過繫統方案進行產前診斷併對預後作齣評估.
목적 탐토태인복수적병인、진단화예후.방법 대79례초성진단위단태태인복수적산전진단결과급임신결국진행회고성분석.결과 79례중,초성제시56례(70.9%)위태인수종종합정표현,23례(29.1%)위단순성복수.56례태인수종종합정중29례(51.8%)반심장확대.병인진단현시79례중,30례위α-중형지중해빈혈,9례궁내감염,3례모태Rh혈형불합,Turner종합정화13일삼체각1례,태인장기기형인기적복수19례,16례병인불명,병인적진단솔79.7%.수방중64례잉부선택종지임신(5례태사궁내),13례족월분면(10례건존,포괄7례태분성복막염화3례특발성복수),2례실방.결론 태인복수병인복잡,α-중형지중해빈혈、태인장기결구기형화궁내감염위주요병인.건의통과계통방안진행산전진단병대예후작출평고.
Objective To investigate the etiology, diagnosis and prognosis of fetal ascites. Methods A retrospective analysis on prenatal diagnosis and pregnant outcomes was performed on 79 singleton pregnancies presenting with fetal ascites through ultrasound scan. Results Among the 79 cases, ultrasound scan indicated 56 cases (70. 9%) of fetal ascites were the menifestation of fetal hydrops and 23 (29. 1%) were isolated cases. Twenty-nine (51.8%) out of the 56 cases of hydrops fetalis presented with cardiac enlargement, and digestive deformities, respiratory and cardiac malformations were commonly seen. Etiology exploration showed 30 cases with alpha-thalassernia, intrauterine infection in 9 cases, organic malformation in 19 cases, 3 cases with matenal-fetal Rhesus alloimmunization, 1 case with Turner syndrome and 1 trisomy-13. The rest 16 cases were idiopathic, thus etiology could be determined in 79. 7% of the 79 cases. During the follow-up, 64 women elected to terminate their pregnancies (5 fetal deaths), 13 full term delivered among which 10 livebom infants survived beyond the neonatal period, including 7 cases of meconium peritonitis and 3 idiopathic ascites, and 2 were lost. Conclusions The etiology of fetal ascites are various, mainly including alpha-thalassemia, organic malformations and intrauterine infection. Isolated fetal ascites, especially fetal ascites caused by meconium peritonitis, have a better prognosis. A systematic protocol is recommended to reach etiology diagnosis and prognosis prediction.