Summary
We here report a case of trisomy 21 with congenital chylothorax. The patient was a male newborn who had been diagnosed as having trisomy 21 with congenital chylothorax. This is the fifth case of the both conditions in English literature. Congenital chylothorax is very rare in a trisomy 21 patient. There, however, may be causal relationship between the two conditions.
Similar content being viewed by others
References
Chernick V, Reed MH (1970) Pneumothorax and chylothorax in the neonatal period. J Pediatr 76:624–632
Ho NK, Leong NKY, Lim SB (1989) Chylothorax in Down's syndrome associated with hydrops fetalis. J Singapore Paediatr Soc 31:90–92
Machin GA (1989) Hydrops revisited: Literature review of 1,414 cases published in the 1980s. Am J Med Genet 34:366–390
Serra A, Neri G (1990) Trisomy 21: Conference report and 1990 update. Am J Med Genet [Suppl] 7:11–19
Van Aerde J, Campbell AN, Smyth JA, Lloyd D, Bryan MH (1984) Spontaneous chylothorax in newborns. A J D C 138:961–964
Yoss BS, Lipsitz PJ (1977) Chylothorax in two mongoloid infants. Clin Genet 12:357–360
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Hamada, H., Fujita, K., Kubo, T. et al. Congenital chylothorax in a trisomy 21 newborn. Arch Gynecol Obstet 252, 55–58 (1992). https://doi.org/10.1007/BF02389608
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF02389608