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Successfully treated congenital cystic adenomatoid malformation by open fetal surgery: A care-compliant case report of a 5-year follow-up and review of the literature
BACKGROUND: Congenital cystic adenomatoid malformation (CCAM) is a rare hamartomatous cystic lesion. Open fetal surgery currently provides a potential therapeutic option for management of a fetus with CCAM diagnosis. CASE SUMMARY: A 22-year-old G2P0 woman presented at [Image: see text] weeks’ gest...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266184/ https://www.ncbi.nlm.nih.gov/pubmed/28079822 http://dx.doi.org/10.1097/MD.0000000000005865 |
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author | Fan, Dazhi Wu, Shuzhen Wang, Rui Huang, Yi Fu, Yao Ai, Wen Zeng, Meng Guo, Xiaoling Liu, Zhengping |
author_facet | Fan, Dazhi Wu, Shuzhen Wang, Rui Huang, Yi Fu, Yao Ai, Wen Zeng, Meng Guo, Xiaoling Liu, Zhengping |
author_sort | Fan, Dazhi |
collection | PubMed |
description | BACKGROUND: Congenital cystic adenomatoid malformation (CCAM) is a rare hamartomatous cystic lesion. Open fetal surgery currently provides a potential therapeutic option for management of a fetus with CCAM diagnosis. CASE SUMMARY: A 22-year-old G2P0 woman presented at [Image: see text] weeks’ gestation for evaluation of a fetus with a left lung lesion and diagnosed as CCAM at [Image: see text] weeks’ gestation. Open fetal surgery was performed to resection the lesion at [Image: see text] weeks’ gestation under deep maternal general anesthesia. The mother presented at [Image: see text] weeks after open fetal surgery with preterm premature rupture of membranes (PPROM) and underwent cesarean delivery at [Image: see text] weeks’ gestation. A vigorous woman infant of 1955 g, with good Apgar score, was delivered. At 1 month, 4 years, and present, 5 years after birth, she has continued to do well without any obvious deficit and both respiration and circulation were well maintained. CONCLUSION: We present one case of CCAM which was cured by open fetal surgery and continued to do well at follow-up of 5 years. The success of treatment provided preliminary experience for further carrying out such interventions in China. |
format | Online Article Text |
id | pubmed-5266184 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-52661842017-02-07 Successfully treated congenital cystic adenomatoid malformation by open fetal surgery: A care-compliant case report of a 5-year follow-up and review of the literature Fan, Dazhi Wu, Shuzhen Wang, Rui Huang, Yi Fu, Yao Ai, Wen Zeng, Meng Guo, Xiaoling Liu, Zhengping Medicine (Baltimore) 7100 BACKGROUND: Congenital cystic adenomatoid malformation (CCAM) is a rare hamartomatous cystic lesion. Open fetal surgery currently provides a potential therapeutic option for management of a fetus with CCAM diagnosis. CASE SUMMARY: A 22-year-old G2P0 woman presented at [Image: see text] weeks’ gestation for evaluation of a fetus with a left lung lesion and diagnosed as CCAM at [Image: see text] weeks’ gestation. Open fetal surgery was performed to resection the lesion at [Image: see text] weeks’ gestation under deep maternal general anesthesia. The mother presented at [Image: see text] weeks after open fetal surgery with preterm premature rupture of membranes (PPROM) and underwent cesarean delivery at [Image: see text] weeks’ gestation. A vigorous woman infant of 1955 g, with good Apgar score, was delivered. At 1 month, 4 years, and present, 5 years after birth, she has continued to do well without any obvious deficit and both respiration and circulation were well maintained. CONCLUSION: We present one case of CCAM which was cured by open fetal surgery and continued to do well at follow-up of 5 years. The success of treatment provided preliminary experience for further carrying out such interventions in China. Wolters Kluwer Health 2017-01-13 /pmc/articles/PMC5266184/ /pubmed/28079822 http://dx.doi.org/10.1097/MD.0000000000005865 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 7100 Fan, Dazhi Wu, Shuzhen Wang, Rui Huang, Yi Fu, Yao Ai, Wen Zeng, Meng Guo, Xiaoling Liu, Zhengping Successfully treated congenital cystic adenomatoid malformation by open fetal surgery: A care-compliant case report of a 5-year follow-up and review of the literature |
title | Successfully treated congenital cystic adenomatoid malformation by open fetal surgery: A care-compliant case report of a 5-year follow-up and review of the literature |
title_full | Successfully treated congenital cystic adenomatoid malformation by open fetal surgery: A care-compliant case report of a 5-year follow-up and review of the literature |
title_fullStr | Successfully treated congenital cystic adenomatoid malformation by open fetal surgery: A care-compliant case report of a 5-year follow-up and review of the literature |
title_full_unstemmed | Successfully treated congenital cystic adenomatoid malformation by open fetal surgery: A care-compliant case report of a 5-year follow-up and review of the literature |
title_short | Successfully treated congenital cystic adenomatoid malformation by open fetal surgery: A care-compliant case report of a 5-year follow-up and review of the literature |
title_sort | successfully treated congenital cystic adenomatoid malformation by open fetal surgery: a care-compliant case report of a 5-year follow-up and review of the literature |
topic | 7100 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266184/ https://www.ncbi.nlm.nih.gov/pubmed/28079822 http://dx.doi.org/10.1097/MD.0000000000005865 |
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