Outcome of congenital cystic adenomatoid malformation of the lung after antenatal diagnosis

C. C. Hsieh; A. S. Chao; Y. L. Chang; D. M. Kuo; T. T. Hsieh; H. T. Hung

doi:10.1016/j.ijgo.2004.11.031

Outcome of congenital cystic adenomatoid malformation of the lung after antenatal diagnosis

C. C. Hsieh, A. S. Chao, Y. L. Chang, D. M. Kuo^*, T. T. Hsieh, H. T. Hung

^*Corresponding author for this work

Chang Gung Memorial Hospital

Research output: Contribution to journal › Journal Article › peer-review

30 Scopus citations

Abstract

Objective: We evaluated the outcome of fetuses diagnosed with having congenital cystic adenomatoid malformation (CCAM) on ultrasonographic examination and managed conservatively. Methods: A retrospective study of 19 cases of CCAM diagnosed antenatally in our hospital was conducted between 1990 and 2001. Complete clinical information was available for all patients, with a mean follow-up of 62 months. Results: The median gestational age at which CCAM was diagnosed was 23 weeks and there were eight live births. With conservative postnatal management, seven neonates had no major complications and one developed bronchopneumonia. Conclusion: Taken together, the findings of the present study and a review of the literature strongly support the conservative management of selected neonates with CCAM.

Original language	English
Pages (from-to)	99-102
Number of pages	4
Journal	International Journal of Gynecology and Obstetrics
Volume	89
Issue number	2
DOIs	https://doi.org/10.1016/j.ijgo.2004.11.031
State	Published - 05 2005
Externally published	Yes

Keywords

Congenital anomalies
Congenital cystic adenomatoid malformation of the lung
Outcome
Prenatal diagnosis

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10.1016/j.ijgo.2004.11.031

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title = "Outcome of congenital cystic adenomatoid malformation of the lung after antenatal diagnosis",

abstract = "Objective: We evaluated the outcome of fetuses diagnosed with having congenital cystic adenomatoid malformation (CCAM) on ultrasonographic examination and managed conservatively. Methods: A retrospective study of 19 cases of CCAM diagnosed antenatally in our hospital was conducted between 1990 and 2001. Complete clinical information was available for all patients, with a mean follow-up of 62 months. Results: The median gestational age at which CCAM was diagnosed was 23 weeks and there were eight live births. With conservative postnatal management, seven neonates had no major complications and one developed bronchopneumonia. Conclusion: Taken together, the findings of the present study and a review of the literature strongly support the conservative management of selected neonates with CCAM.",

keywords = "Congenital anomalies, Congenital cystic adenomatoid malformation of the lung, Outcome, Prenatal diagnosis",

author = "Hsieh, {C. C.} and Chao, {A. S.} and Chang, {Y. L.} and Kuo, {D. M.} and Hsieh, {T. T.} and Hung, {H. T.}",

year = "2005",

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doi = "10.1016/j.ijgo.2004.11.031",

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volume = "89",

pages = "99--102",

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AU - Hsieh, C. C.

AU - Chao, A. S.

AU - Chang, Y. L.

AU - Kuo, D. M.

AU - Hsieh, T. T.

AU - Hung, H. T.

PY - 2005/5

Y1 - 2005/5

N2 - Objective: We evaluated the outcome of fetuses diagnosed with having congenital cystic adenomatoid malformation (CCAM) on ultrasonographic examination and managed conservatively. Methods: A retrospective study of 19 cases of CCAM diagnosed antenatally in our hospital was conducted between 1990 and 2001. Complete clinical information was available for all patients, with a mean follow-up of 62 months. Results: The median gestational age at which CCAM was diagnosed was 23 weeks and there were eight live births. With conservative postnatal management, seven neonates had no major complications and one developed bronchopneumonia. Conclusion: Taken together, the findings of the present study and a review of the literature strongly support the conservative management of selected neonates with CCAM.

AB - Objective: We evaluated the outcome of fetuses diagnosed with having congenital cystic adenomatoid malformation (CCAM) on ultrasonographic examination and managed conservatively. Methods: A retrospective study of 19 cases of CCAM diagnosed antenatally in our hospital was conducted between 1990 and 2001. Complete clinical information was available for all patients, with a mean follow-up of 62 months. Results: The median gestational age at which CCAM was diagnosed was 23 weeks and there were eight live births. With conservative postnatal management, seven neonates had no major complications and one developed bronchopneumonia. Conclusion: Taken together, the findings of the present study and a review of the literature strongly support the conservative management of selected neonates with CCAM.

KW - Congenital anomalies

KW - Congenital cystic adenomatoid malformation of the lung

KW - Outcome

KW - Prenatal diagnosis

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Outcome of congenital cystic adenomatoid malformation of the lung after antenatal diagnosis

Abstract

Keywords

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