Miny P, Hammer P, Gerlach B, Tercanli S, Horst J, Holzgreve W, Eiben B
Institut für Humangenetik, University of Münster, Germany.
Prenat Diagn. 1991 Aug;11(8):581-9. doi: 10.1002/pd.1970110815.
Discrepant chromosome findings in placenta and fetus (false negative and false positive) after chorionic villus sampling (CVS) are mainly due to confined mosaicism. Non-mosaic normal or abnormal chromosome counts after direct preparation and culture nearly always correctly reflect the fetal chromosome constitution. False-negative results have almost exclusively been restricted to cytotrophoblast cells not representing a fetal chromosome abnormality. Diagnosis of placental mosaicism definitely requires an adequate follow-up by amniocentesis, fetal blood sampling, or sonography before a pregnancy is terminated. When direct preparations and cultured cells are used for cytogenetic diagnoses and placental mosaicism is not taken as proof for a chromosomal abnormality in the fetus, CVS is an accurate diagnostic tool.
绒毛取样(CVS)后胎盘和胎儿出现染色体结果不一致(假阴性和假阳性)主要是由于局限性嵌合体。直接制片和培养后非嵌合的正常或异常染色体计数几乎总能正确反映胎儿的染色体构成。假阴性结果几乎完全局限于不代表胎儿染色体异常的细胞滋养层细胞。在终止妊娠前,胎盘嵌合体的诊断绝对需要通过羊膜穿刺术、胎儿采血或超声进行充分的随访。当直接制片和培养细胞用于细胞遗传学诊断且胎盘嵌合体不作为胎儿染色体异常的证据时,绒毛取样是一种准确的诊断工具。