[Retrocervical cystic hygroma: diagnosis, prognosis and management. A series of 13 cases].
Identifieur interne : 003D12 ( Ncbi/Checkpoint ); précédent : 003D11; suivant : 003D13[Retrocervical cystic hygroma: diagnosis, prognosis and management. A series of 13 cases].
Auteurs : S. Douvier ; J P Feldman ; A. Nivelon-Chevalier ; M. Degrolard ; M H Harran ; J. JahierSource :
- Journal de gynecologie, obstetrique et biologie de la reproduction [ 0368-2315 ] ; 1991.
Descripteurs français
- KwdFr :
- Adulte, Caryotypage, Femelle, Grossesse, Humains, Lymphangiome (anatomopathologie), Lymphangiome (génétique), Lymphangiome (imagerie diagnostique), Maladies foetales (anatomopathologie), Maladies foetales (génétique), Maladies foetales (imagerie diagnostique), Maladies lymphatiques (anatomopathologie), Maladies lymphatiques (génétique), Maladies lymphatiques (imagerie diagnostique), Phénotype, Pronostic, Échographie prénatale, Études rétrospectives.
- MESH :
- anatomopathologie : Lymphangiome, Maladies foetales, Maladies lymphatiques.
- génétique : Lymphangiome, Maladies foetales, Maladies lymphatiques.
- imagerie diagnostique : Lymphangiome, Maladies foetales, Maladies lymphatiques.
- Adulte, Caryotypage, Femelle, Grossesse, Humains, Phénotype, Pronostic, Échographie prénatale, Études rétrospectives.
English descriptors
- KwdEn :
- Adult, Female, Fetal Diseases (diagnostic imaging), Fetal Diseases (genetics), Fetal Diseases (pathology), Humans, Karyotyping, Lymphangioma (diagnostic imaging), Lymphangioma (genetics), Lymphangioma (pathology), Lymphatic Diseases (diagnostic imaging), Lymphatic Diseases (genetics), Lymphatic Diseases (pathology), Phenotype, Pregnancy, Prognosis, Retrospective Studies, Ultrasonography, Prenatal.
- MESH :
- diagnostic imaging : Fetal Diseases, Lymphangioma, Lymphatic Diseases.
- genetics : Fetal Diseases, Lymphangioma, Lymphatic Diseases.
- pathology : Fetal Diseases, Lymphangioma, Lymphatic Diseases.
- Adult, Female, Humans, Karyotyping, Phenotype, Pregnancy, Prognosis, Retrospective Studies, Ultrasonography, Prenatal.
Abstract
Fetal cystic hygroma (CH) are congenital malformation of the lymphatic system which are seen in antenatally ultrasonography from the end of the first trimester of pregnancy. From a 13 CH retrospective study, the authors discuss the ultrasound diagnosis, the prognosis and the management of CH. In our study, CH is associated with lymphedema (69%), hydrops (46%), diminution of amniotic fluid (69%) and other abnormality (31%). In all cases a diminution or an absence of fetal movement are found. In seven cases a cytogenetic analysis are performed on amniocentesis or fetal tissues: there are five 45XO, one 47XX + 13 and one 46XX. In six cases the chromosome culture failed: two male phenotypes and two histologic appearances of chromosomic anomaly. The prognosis depends on chromosome analysis, other ultrasound abnormality and the size of CH. It is usually fatal in utero. If chromosome anomaly are found, a genetic counsel is proposed.
PubMed: 2071861
Affiliations:
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A series of 13 cases].</title><author><name sortKey="Douvier, S" sort="Douvier, S" uniqKey="Douvier S" first="S" last="Douvier">S. Douvier</name><affiliation><nlm:affiliation>Clinique Gynécologique et Obstétricale, CHU, Dijon.</nlm:affiliation><wicri:noCountry code="subField">Dijon</wicri:noCountry></affiliation></author><author><name sortKey="Feldman, J P" sort="Feldman, J P" uniqKey="Feldman J" first="J P" last="Feldman">J P Feldman</name></author><author><name sortKey="Nivelon Chevalier, A" sort="Nivelon Chevalier, A" uniqKey="Nivelon Chevalier A" first="A" last="Nivelon-Chevalier">A. Nivelon-Chevalier</name></author><author><name sortKey="Degrolard, M" sort="Degrolard, M" uniqKey="Degrolard M" first="M" last="Degrolard">M. Degrolard</name></author><author><name sortKey="Harran, M H" sort="Harran, M H" uniqKey="Harran M" first="M H" last="Harran">M H Harran</name></author><author><name sortKey="Jahier, J" sort="Jahier, J" uniqKey="Jahier J" first="J" last="Jahier">J. Jahier</name></author></analytic><series><title level="j">Journal de gynecologie, obstetrique et biologie de la reproduction</title><idno type="ISSN">0368-2315</idno><imprint><date when="1991" type="published">1991</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term><term>Female</term><term>Fetal Diseases (diagnostic imaging)</term><term>Fetal Diseases (genetics)</term><term>Fetal Diseases (pathology)</term><term>Humans</term><term>Karyotyping</term><term>Lymphangioma (diagnostic imaging)</term><term>Lymphangioma (genetics)</term><term>Lymphangioma (pathology)</term><term>Lymphatic Diseases (diagnostic imaging)</term><term>Lymphatic Diseases (genetics)</term><term>Lymphatic Diseases (pathology)</term><term>Phenotype</term><term>Pregnancy</term><term>Prognosis</term><term>Retrospective Studies</term><term>Ultrasonography, Prenatal</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Adulte</term><term>Caryotypage</term><term>Femelle</term><term>Grossesse</term><term>Humains</term><term>Lymphangiome (anatomopathologie)</term><term>Lymphangiome (génétique)</term><term>Lymphangiome (imagerie diagnostique)</term><term>Maladies foetales (anatomopathologie)</term><term>Maladies foetales (génétique)</term><term>Maladies foetales (imagerie diagnostique)</term><term>Maladies lymphatiques (anatomopathologie)</term><term>Maladies lymphatiques (génétique)</term><term>Maladies lymphatiques (imagerie diagnostique)</term><term>Phénotype</term><term>Pronostic</term><term>Échographie prénatale</term><term>Études rétrospectives</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Lymphangiome</term><term>Maladies foetales</term><term>Maladies lymphatiques</term></keywords><keywords scheme="MESH" qualifier="diagnostic imaging" xml:lang="en"><term>Fetal Diseases</term><term>Lymphangioma</term><term>Lymphatic Diseases</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Fetal Diseases</term><term>Lymphangioma</term><term>Lymphatic Diseases</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Lymphangiome</term><term>Maladies foetales</term><term>Maladies lymphatiques</term></keywords><keywords scheme="MESH" qualifier="imagerie diagnostique" xml:lang="fr"><term>Lymphangiome</term><term>Maladies foetales</term><term>Maladies lymphatiques</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Fetal Diseases</term><term>Lymphangioma</term><term>Lymphatic Diseases</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Female</term><term>Humans</term><term>Karyotyping</term><term>Phenotype</term><term>Pregnancy</term><term>Prognosis</term><term>Retrospective Studies</term><term>Ultrasonography, Prenatal</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Adulte</term><term>Caryotypage</term><term>Femelle</term><term>Grossesse</term><term>Humains</term><term>Phénotype</term><term>Pronostic</term><term>Échographie prénatale</term><term>Études rétrospectives</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Fetal cystic hygroma (CH) are congenital malformation of the lymphatic system which are seen in antenatally ultrasonography from the end of the first trimester of pregnancy. From a 13 CH retrospective study, the authors discuss the ultrasound diagnosis, the prognosis and the management of CH. In our study, CH is associated with lymphedema (69%), hydrops (46%), diminution of amniotic fluid (69%) and other abnormality (31%). In all cases a diminution or an absence of fetal movement are found. In seven cases a cytogenetic analysis are performed on amniocentesis or fetal tissues: there are five 45XO, one 47XX + 13 and one 46XX. In six cases the chromosome culture failed: two male phenotypes and two histologic appearances of chromosomic anomaly. The prognosis depends on chromosome analysis, other ultrasound abnormality and the size of CH. It is usually fatal in utero. If chromosome anomaly are found, a genetic counsel is proposed.</div></front></TEI><affiliations><list></list><tree><noCountry><name sortKey="Degrolard, M" sort="Degrolard, M" uniqKey="Degrolard M" first="M" last="Degrolard">M. 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