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Isolated fetal lymphatic malformation of the thigh: prenatal diagnosis and follow-up
Durukan, Huseyin; Gözükara, Ilay; Cevikoglu, Murside; Dilek, Talat Umut Kutlu.
Afiliação
  • Durukan, Huseyin; Mersin University. Faculty of Medicine. Department of Obstetrics and Gynecology. Mersin. TR
  • Gözükara, Ilay; Mustafa Kemal University. Faculty of Medicine. Department of Obstetrics and Gynecology. Hatay. TR
  • Cevikoglu, Murside; Mersin University. Faculty of Medicine. Department of Obstetrics and Gynecology. Mersin. BR
  • Dilek, Talat Umut Kutlu; Acibadem Atakent University Hospital. Faculty of Medicine. Department of Obstetrics and Gynecology. Istanbul. TR
Autops. Case Rep ; 7(1): 49-53, Jan.-Mar. 2017. ilus
Article em En | LILACS | ID: biblio-905134
Biblioteca responsável: BR26.7
ABSTRACT
Fetal lymphatic malformation can be found in different parts of the fetal body. It occurs most frequently in the nuchal and axillary region and less frequently in the abdomen or inguinal areas. Lymphatic malformation has been associated with fetal aneuploidy, hydrops fetalis, structural malformations, and intrauterine fetal death. A 31-year-old gravida 3, para 2 woman was admitted to our hospital at 22 weeks of gestation (confirmed by ultrasonographic examination). The fetus was alive, and had a mass derived from the left inguinal region extending to the anterior left leg with fluid-filled cavities about 3-5 cm in size. There was no evidence of intra-abdominal extension of the mass. Amniocentesis was performed. Fetal magnetic resonance imaging revealed a left inguinal cystic mass, which extended to the left thigh. Antenatal follow-up was uneventful. The mother gave birth at term with a cesarean section. Postnatal clinical examination and imaging examination confirmed the diagnosis of lymphatic malformation. Fetal lymphatic malformation carries a high risk of aneuploidy and fetal malformations. Patients diagnosed with lymphatic malformation in antenatal follow-up should be assessed in terms of coexistent anomalies. Fetal karyotyping should be done and the fetus should be monitored for fetal hydrops.
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Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS Assunto principal: Coxa da Perna / Anormalidades Linfáticas / Doenças Fetais Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Autops. Case Rep Assunto da revista: Anatomia / Patologia Cl¡nica / Patologia Legal Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Turquia

Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS Assunto principal: Coxa da Perna / Anormalidades Linfáticas / Doenças Fetais Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Autops. Case Rep Assunto da revista: Anatomia / Patologia Cl¡nica / Patologia Legal Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Turquia