One hundred three consecutive patients with anorectal malformations and their associated anomalies

被引:83
作者
Cho, S [1 ]
Moore, SP [1 ]
Fangman, T [1 ]
机构
[1] Univ Kansas, Sch Med, Dept Pediat, Wichita, KS 67214 USA
来源
ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE | 2001年 / 155卷 / 05期
关键词
D O I
10.1001/archpedi.155.5.587
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective: A long-term retrospective analysis of 103 infants with anorectal malformations (ARMs) was con ducted to describe any associated congenital anomalies and surgical classifications. Design: Retrospective medical record review. Setting: This case series was conducted on all infants with ARMs born at, or referred to, any of 3 major medical centers in Wichita, Kan, for close to a 22-year period. Patients: The 103 infants in this study represent a consecutive sample of patients with ARMs. Patients were separated into 2 groups: isolated ARMs without associated anomalies (n=30), and ARMs with associated anomalies (n=73), The male-female ratio was 2:1. Main Outcome Measures: Patients with associated anomalies were further classified into groups of ARMs with minor anomalies; major anomalies; chromosomal abnormalities; and malformation syndromes, associations, or sequences. Only anomalies that occurred mure than once were reported. Malformations were also classified according to major organ systems. Results: The incidence of ARMs in our study was approximately 1 in 2500 live births. Additional anomalies were found in 71% of infants with ARMs. Associated anomalies by major organ system included genitourinary anomalies (49%), musculoskeletal anomalies (43%), craniofacial anomalies (34%), cardiovascular anomalies (27%), gastrointestinal anomalies (18%), respiratory anomalies (13%), and central nervous system anomalies (12%). The most common chromosomal abnormalities were trisomies (8%), and ARMs were associated with VATER complex (vertebral defects, anal atresia, tracheoesophageal fistula with esophageal atresia, and radial and renal anomalies) in 11 cases (11%) and VACTERL (vertebral, anal, cardiac, tracheal, esophageal, renal, and limb anomalies) in 4 cases (4%). Conclusions: Patients with ARMs have a high incidence of associated congenital anomalies. Evaluation of the most commonly affected organ systems in these infants is essential because it is these associated anomalies that account for most of the morbidity and mortality that is associated with this condition.
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收藏
页码:587 / 591
页数:5
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