Outcome and treatment in an antenatally diagnosed congenital cystic adenomatoid malformation of the lung |
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Authors: | Kouji Nagata Kouji Masumoto Risa Tesiba Genshirou Esumi Kiyomi Tsukimori Wake Norio Tomoaki Taguchi |
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Affiliation: | (1) Department of Pediatric Surgery, Reproductive and Developmental Medicine, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku Fukuoka, 812-8582, Japan;(2) Department of Obstetrics and Gynecology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan; |
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Abstract: |
Background The natural history of patients with antenatally diagnosed congenital cystic adenomatoid malformation of the lung (CCAM) is still fully unknown. In symptomatic patients with respiratory distress, an operation is performed during the neonatal period. However, in asymptomatic patients, the optimal timing of the operation remains controversial. During the period from 1977 to 2007, we experienced 14 CCAM patients diagnosed antenatally. Therefore, we investigated the outcome of antenatally diagnosed CCAM patients to clarify the optimal treatment for such patients. |
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