An incidental finding of maternal multiple myeloma by non invasive prenatal testing

被引：10

作者：

Imbert-Bouteille, Marion ^{[1
,2
]}

Chiesa, Jean ^{[1
]}

Gaillard, Jean-Baptiste ^{[1
]}

Dorvaux, Veronique ^{[3
]}

Altounian, Lucille ^{[4
]}

Gatinois, Vincent ^{[2
]}

Mousty, Eve ^{[5
]}

Finge, Sanae ^{[6
]}

Bourquard, Pascal ^{[7
]}

Vermeesch, Joris Robert ^{[8
,9
]}

Legius, Eric ^{[8
,9
]}

Vandenberghe, Peter ^{[8
,9
]}

机构：

[1] Caremeau Univ Hosp Ctr, Med Genet & Cytogenet Dept, Nimes, France

[2] Univ Hosp Ctr, Med Genet & Cytogenet Dept, Montpellier, France

[3] Mercy Hosp Ctr Metz Thionville, Dept Hematol, Metz, France

[4] Mercy Hosp Ctr Metz Thionville, Dept Cytogenet, Metz, France

[5] Caremeau Univ Hosp Ctr, Multidisciplinary Prenatal Diag Dept, Nimes, France

[6] Caremeau Univ Hosp Ctr, Biol & Immunol Dept, Nimes, France

[7] Caremeau Univ Hosp Ctr, Dept Clin Hematol, Nimes, France

[8] Univ Hosp Leuven, Dept Human Genet, Ctr Human Genet, Leuven, Belgium

[9] Univ Hosp Leuven, Dept Hematol, Leuven, Belgium

来源：

PRENATAL DIAGNOSIS | 2017年 / 37卷 / 12期

关键词：

PREGNANCY; CANCER;

D O I：

10.1002/pd.5168

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

What is already known about this subject? Non invasive prenatal testing for fetal trisomies 13, 18, and 21 occasionally identifies maternal cancer. What does this study add? A further case of maternal cancer incidentally diagnosed by routine NIPT. Extensive NIPT abnormalities are unlikely to be of fetal origin. Information given to patients should also adequately advise patients on potential incidental findings and might offer the option to opt out of receiving results beyond the trisomy report. International guidelines would improve patient counseling.

引用

页码：1257 / 1260

页数：4

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