Search

Objectives: Our aim was to evaluate ultrasound findings and perinatal outcome after prenatal diagnosis of lymphangioma., Methods: This was a retrospective case series study. We searched the archives of our ultrasound database at our center for cases with the prenatal diagnosis of the lymphangioma in the period between January 2008 and November 2014. We described maternal, fetal and perinatal variables for all cases., Results: Nine fetuses with lymphangioma were identified. All cases were diagnosed during the second and third trimesters with the average gestational age of 22.6 ± 3.9 weeks. The average diameter of lymphangioma was 55.4 ± 20.1 mm at the time of diagnosis. Five fetuses (55.6%) had lymphangioma on the neck, and four fetuses (44.4%) had lymphangioma on other localizations. Normal fetal karyotype was detected in all cases. There were a total of six live births, one intrauterine death and two medical terminations of pregnancy following the diagnosis of lymphangioma. No abnormal Doppler finding or hydrops were detected in the antenatal follow-up of remaining six cases., Conclusion: The risk of chromosomal abnormalities is very low in pregnancies with isolated lymphangioma. The outcome of pregnancies with lymphangioma is generally favorable and prognosis depends on their locations and size.

Objective: Our aim was to evaluate ultrasound findings and perinatal outcome after prenatal diagnosis of lymphangiomas Methods: We searched the archives of our ultrasound database at our center for cases with a prenatal diagnosis of the lymphangioma in the period from 2008 to 2013. We described maternal, fetal and perinatal variables for all cases. Results: Seven fetuses were diagnosed in our center as having the lymphangioma between 2008 and 2013. All cases were diagnosed during the second and third trimesters with the average gestational age of 24±4 weeks. The average diameter of lymphangioma were 58.4±22.5 mm at time of diagnosis. Four of the seven fetuses (57.1%) had lymphangioma in the neck. Three of the seven fetuses (42.9%) had lymphangioma in locations other than fetal neck. Fetal karyotyping was normal in all cases. Two of these fetuses was terminated. No abnormal doppler finding or hydrops were detected in the antenatal follow-up of remaining five cases. Cesarean section was performed due to dystocia for all cases. Conclusion: The risk of chromosomal abnormalities is very low in pregnancies with isolated lymphangioma. The outcome of pregnancies with lymphangioma is generally favorable and prognosis depends on their locations and size. [ABSTRACT FROM AUTHOR]