Tennstedt C, Chaoui R, Körner H, Dietel M
Department of Pathology, Charité Hospital of the Humboldt University, Berlin, Germany.
Heart. 1999 Jul;82(1):34-9. doi: 10.1136/hrt.82.1.34.
To analyse the spectrum of congenital heart malformations, the frequency of extracardiac malformations, and the proportion of chromosome aberrations among fetuses sent for necropsy.
Necropsies were performed on 815 fetuses-448 induced abortions (55%), 220 spontaneous abortions (27%), and 147 stillbirths (18%)-during a seven year period (1991-97) in the department of pathology of the Charité Medical Centre in Berlin. A congenital heart defect was identified in 129 cases (16%). For all 129 fetuses, karyotyping and an ultrasound examination had been performed.
Congenital heart defects were present in 22% of induced abortions (99 cases), 9% of spontaneous abortions (20 cases), and 7% of stillbirths (10 cases). The heart malformations were classified into 13 categories. A fetus with more than one defect was included only in the category of the most serious defect. The malformations in order of frequency were: ventricular septal defect (VSD) (28%), atrioventricular septal defect (AVSD) (16%), hypoplastic left heart (HLH) (16%), double outlet right ventricle (DORV) (12%), coarctation of the aorta (CoA) (6%), transposition of the great arteries (TGA) (4%), aortic valve stenosis (AoVS) (4%), tetralogy of Fallot (TOF) (3%), truncus arteriosus communis (TAC) (3%), pulmonary valve stenosis/pulmonary valve atresia (PaVS/PaVA) (3%), tricuspid atresia (TA) (3%), single ventricle (SV) (1.5%), and atrial septal defect (ASD) (0.5%). The most common congenital heart defects were VSD, AVSD, HLH, and DORV, which made up 72% of all the cases. In 11 cases the heart defect was isolated (no other cardiovascular or extracardiac malformations present), 85 cases (66%) were associated with additional cardiac malformations, 85 cases (66%) were associated with extracardiac malformations, and chromosome anomalies were detected in 43 cases (33%).
Fetal congenital heart malformations are common. These defects are often associated with other cardiovascular and extracardiac malformations, as well as with chromosome anomalies. Complex heart defects such as AVSD, HLH, and DORV are frequent in fetuses, as they often lead to spontaneous abortion or stillbirth or, after prenatal diagnosis, to deliberate termination of pregnancy.
分析送检尸检胎儿的先天性心脏畸形谱、心外畸形频率及染色体畸变比例。
在柏林夏里特医学中心病理科的七年期间(1991 - 1997年),对815例胎儿进行了尸检,其中448例为人工流产(55%),220例为自然流产(27%),147例为死产(18%)。129例(16%)被鉴定出有先天性心脏缺陷。对所有129例胎儿都进行了染色体核型分析和超声检查。
人工流产胎儿中22%(99例)有先天性心脏缺陷,自然流产胎儿中9%(20例)有先天性心脏缺陷,死产胎儿中7%(10例)有先天性心脏缺陷。心脏畸形分为13类。有多种缺陷的胎儿仅归入最严重缺陷类别。畸形出现频率依次为:室间隔缺损(VSD)(28%)、房室间隔缺损(AVSD)(16%)、左心发育不全(HLH)(16%)、右心室双出口(DORV)(12%)、主动脉缩窄(CoA)(6%)、大动脉转位(TGA)(4%)、主动脉瓣狭窄(AoVS)(4%)、法洛四联症(TOF)(3%)、共同动脉干(TAC)(3%)、肺动脉瓣狭窄/肺动脉瓣闭锁(PaVS/PaVA)(3%)、三尖瓣闭锁(TA)(3%)、单心室(SV)(1.5%)、房间隔缺损(ASD)(0.5%)。最常见的先天性心脏缺陷是VSD、AVSD、HLH和DORV,占所有病例的72%。11例心脏缺陷为孤立性(无其他心血管或心外畸形),85例(66%)伴有其他心脏畸形,85例(66%)伴有心外畸形,43例(33%)检测到染色体异常。
胎儿先天性心脏畸形很常见。这些缺陷常与其他心血管和心外畸形以及染色体异常相关。复杂心脏缺陷如AVSD、HLH和DORV在胎儿中很常见,因为它们常导致自然流产或死产,或在产前诊断后导致人工终止妊娠。