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

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 af...

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Main Authors: Donghao Lu, Yuhe Wang, Weiyue Zeng, Bing Peng
Format: Article
Language:English
Published: Elsevier 2015-02-01
Series:Taiwanese Journal of Obstetrics & Gynecology
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1028455914002095
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spelling doaj-280c5dc8b769414eb2d75092314cd7612020-11-24T20:51:02ZengElsevierTaiwanese Journal of Obstetrics & Gynecology1028-45592015-02-01541626510.1016/j.tjog.2014.11.009Giant fetal lymphangioma at chest wall and prognosis: Case report and literature reviewDonghao Lu0Yuhe Wang1Weiyue Zeng2Bing Peng3Department of Obstetrics and Gynecology, West China Second University Hospital, Sichuan University, Chengdu, ChinaDepartment of Obstetrics and Gynecology, West China Second University Hospital, Sichuan University, Chengdu, ChinaDepartment of Obstetrics and Gynecology, West China Second University Hospital, Sichuan University, Chengdu, ChinaDepartment of Obstetrics and Gynecology, West China Second University Hospital, Sichuan University, Chengdu, ChinaObjective: 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 × 9.2 cm × 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.http://www.sciencedirect.com/science/article/pii/S1028455914002095congenital malformationsgenetic counselinglymphangiomaprenatal diagnosis
collection DOAJ
language English
format Article
sources DOAJ
author Donghao Lu
Yuhe Wang
Weiyue Zeng
Bing Peng
spellingShingle Donghao Lu
Yuhe Wang
Weiyue Zeng
Bing Peng
Giant fetal lymphangioma at chest wall and prognosis: Case report and literature review
Taiwanese Journal of Obstetrics & Gynecology
congenital malformations
genetic counseling
lymphangioma
prenatal diagnosis
author_facet Donghao Lu
Yuhe Wang
Weiyue Zeng
Bing Peng
author_sort Donghao Lu
title Giant fetal lymphangioma at chest wall and prognosis: Case report and literature review
title_short Giant fetal lymphangioma at chest wall and prognosis: Case report and literature review
title_full Giant fetal lymphangioma at chest wall and prognosis: Case report and literature review
title_fullStr Giant fetal lymphangioma at chest wall and prognosis: Case report and literature review
title_full_unstemmed Giant fetal lymphangioma at chest wall and prognosis: Case report and literature review
title_sort giant fetal lymphangioma at chest wall and prognosis: case report and literature review
publisher Elsevier
series Taiwanese Journal of Obstetrics & Gynecology
issn 1028-4559
publishDate 2015-02-01
description 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 × 9.2 cm × 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.
topic congenital malformations
genetic counseling
lymphangioma
prenatal diagnosis
url http://www.sciencedirect.com/science/article/pii/S1028455914002095
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AT yuhewang giantfetallymphangiomaatchestwallandprognosiscasereportandliteraturereview
AT weiyuezeng giantfetallymphangiomaatchestwallandprognosiscasereportandliteraturereview
AT bingpeng giantfetallymphangiomaatchestwallandprognosiscasereportandliteraturereview
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