Giant fetal lymphangioma at chest wall and prognosis: Case report and literature review

被引:10
|
作者
Lu, Donghao [1 ,2 ]
Wang, Yuhe [1 ]
Zeng, Weiyue [1 ]
Peng, Bing [1 ]
机构
[1] Sichuan Univ, West China Univ Hosp 2, Dept Obstet & Gynecol, Chengdu 610041, Peoples R China
[2] Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden
来源
关键词
congenital malformations; genetic counseling; lymphangioma; prenatal diagnosis; NUCHAL CYSTIC HYGROMA; PRENATAL-DIAGNOSIS; INTRAUTERINE TREATMENT; EXPERIENCE; MANAGEMENT;
D O I
10.1016/j.tjog.2014.11.009
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To report a rare liveborn case with a giant, septated, chest wall lymphangioma that underwent prenatal expectation treatment. Case report: A case of giant fetal chest wall cystic lymphangioma was diagnosed prenatally at 19 weeks gestation. Expectation treatment was performed, carefully after prenatal counseling, ruling out other structural abnormalities. At 38 weeks gestation, ultrasound showed a multilocular, subcutaneous cystic mass of 12.3 cm x 9.2 cm x 11.0 cm located on the left chest wall and left upper arm. The tumor was surgically removed 4 days after birth, and no recurrence was observed in the following 18 months. Conclusion: Our experience suggests that a large, septated fetal lymphangioma may still merit prenatal expectation treatment if there is no evidence for chromosomal and structural abnormality. Copyright (C) 2014, Taiwan Association of Obstetrics & Gynecology. Published by Elsevier Taiwan LLC. All rights reserved.
引用
收藏
页码:62 / 65
页数:4
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