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Spectrum of anorectal anomalies in pygopagus twins.

Authors :
Janik JS
Hendrickson RJ
Janik JP
Bensard DD
Partrick DA
Karrer FM
Source :
Journal of pediatric surgery [J Pediatr Surg] 2003 Apr; Vol. 38 (4), pp. 608-12.
Publication Year :
2003

Abstract

Background/purpose: The literature lacks a concise description of the anorectal anomalies encountered in pygopagus twins.<br />Methods: This is a retrospective literature review of 34 pygopagus twins highlighting their anorectal malformations.<br />Results: Overall pygopagus twins represent 17% of all conjoined twins. Live-birth pygopagus twins are more commonly female (86%), whereas stillborns are commonly male (80%). Half of the twins had nonfused rectums, and half had fused rectums. The nonfused had 2 rectums (80%) or one rectum and one rectovaginal fistula (20%). The fused had high (46%) or low (54%) rectal junctions. All reported living male pygopagus twins have had nonfused rectums. All can be managed applying the principles of posterior sagittal anorectoplasty.<br />Conclusions: In general, live-born male pygopagus twins are likely to survive with a nonfused rectum and good bowel function, whereas live-born female pygopagus twins have a good chance of surviving with a fused rectum (high or low), which requires appropriate operative reconstruction.<br /> (Copyright 2003, Elsevier Science (USA). All rights reserved.)

Details

Language :
English
ISSN :
1531-5037
Volume :
38
Issue :
4
Database :
MEDLINE
Journal :
Journal of pediatric surgery
Publication Type :
Academic Journal
Accession number :
12677576
Full Text :
https://doi.org/10.1053/jpsu.2003.50132