Clinical Presentations and Diagnostic Imaging of VACTERL Association.

IF 0.7 4区 医学 Q4 PATHOLOGY Fetal and Pediatric Pathology Pub Date : 2023-08-01 Epub Date: 2023-05-17 DOI:10.1080/15513815.2023.2206905
Gabriele Tonni, Çağla Koçak, Gianpaolo Grisolia, Giuseppe Rizzo, Edward Araujo Júnior, Heron Werner, Rodrigo Ruano, Waldo Sepulveda, Maria Paola Bonasoni, Mario Lituania
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引用次数: 1

Abstract

Background: VACTERL association consists of Vertebral, Anorectal, Cardiac, Tracheo-Esophageal, Renal, and Limb defects. The diagnosis depends on the presence of at least three of these structural abnormalities. Methods: The clinical presentation and diagnostic prenatal imaging of VACTERL association are comprehensively reviewed. Results: The most common feature is a vertebral anomaly, found in 60-80% of cases. Tracheo-esophageal fistula is seen in 50-80% of cases and renal malformations in 30% of patients. Limb defects including thumb aplasia/hypoplasia, polydactyly, and radial agenesis/hypoplasia are present in 40-50% of cases. Anorectal defects, like imperforate anus/anal atresia, are challenging to detect prenatally. Conclusion: The diagnosis of VACTERL association mostly relies on imaging techniques such as ultrasound, computed tomography, and magnetic resonance. Differential diagnosis should exclude similar diseases such as CHARGE and Townes-Brocks syndromes and Fanconi anemia. New insights into genetic etiology have led to recommendations of chromosomal breakage investigation for optimal diagnosis and counseling.

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VACTERL协会的临床表现和诊断影像学。
背景:VACTERL相关性包括脊椎、肛门直肠、心脏、气管、食道、肾脏和四肢缺陷。诊断取决于这些结构异常中至少有三种的存在。方法:对VACTERL相关性的临床表现和产前影像学诊断进行综合评述。结果:最常见的特征是脊椎异常,在60-80%的病例中发现。50-80%的病例出现气管食管瘘,30%的患者出现肾脏畸形。40-50%的病例存在四肢缺陷,包括拇指发育不全/发育不全、多指和桡骨发育不全或发育不全。肛门直肠缺陷,如肛门闭锁/肛门闭锁,很难在产前发现。结论:VACTERL相关性的诊断主要依赖于超声、计算机断层扫描和磁共振等成像技术。鉴别诊断应排除类似的疾病,如CHARGE和Townes-Brocks综合征以及Fanconi贫血。对遗传病因的新见解导致了染色体断裂调查的建议,以获得最佳诊断和咨询。
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来源期刊
CiteScore
3.00
自引率
0.00%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Fetal and Pediatric Pathology is an established bimonthly international journal that publishes data on diseases of the developing embryo, newborns, children, and adolescents. The journal publishes original and review articles and reportable case reports. The expanded scope of the journal encompasses molecular basis of genetic disorders; molecular basis of diseases that lead to implantation failures; molecular basis of abnormal placentation; placentology and molecular basis of habitual abortion; intrauterine development and molecular basis of embryonic death; pathogenisis and etiologic factors involved in sudden infant death syndrome; the underlying molecular basis, and pathogenesis of diseases that lead to morbidity and mortality in newborns; prenatal, perinatal, and pediatric diseases and molecular basis of diseases of childhood including solid tumors and tumors of the hematopoietic system; and experimental and molecular pathology.
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