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儿童消化道重复畸形:26年经验报告

Alimentary tract duplications in children: report of 26 years' experience.

作者信息

Karnak I, Ocal T, Senocak M E, Tanyel F C, Büyükpamukçu N

机构信息

Department of Pediatric Surgery, Hacettepe University Faculty of Medicine, Ankara, Turkey.

出版信息

Turk J Pediatr. 2000 Apr-Jun;42(2):118-25.

Abstract

Duplications of the alimentary tract are one of the rare anomalies of the gastrointestinal system. Because of the wide spectrum of the signs and symptoms, preoperative diagnosis frequently cannot be made. A close familiarity with clinical and surgical characteristics provides appropriate management and treatment of duplications. A retrospective clinical study was conducted to evaluate clinical and surgical characteristics and the treatment of duplications of the alimentary tract. During a 26-year period between 1971 and 1997, 38 patients with duplications of alimentary tract underwent operation at the Hacettepe University Department of Pediatric Surgery. Forty-two duplications in 38 patients (20 male, 53%; 18 female, 47%) were encountered. Sixty-nine percent of the patients were symptomatic under the age of one year, with 24 percent presenting with symptoms in the neonatal period. There were one sublingual, nine intrathoracic (including 2 thoracoabdominal) and 32 intraabdominal duplications. Abdominal mass, abdominal distention, constipation, vomiting and respiratory distress were the most frequently encountered signs and symptoms. Plain thoracic and abdominal X-rays, ultrasonography, and computed tomography of the chest and abdomen were the most commonly used diagnostic radiological methods. Thirty-three duplications (79%) were spherical and nine (21%) were tubular. Multiple duplications were encountered in two patients (5.3%). Fourteen duplications (33%) contained heterotopic mucosa, mostly gastric type. More than one type of heterotopic mucosa in the same duplication was encountered in four duplications (10%). Additional malformations were encountered in 26 percent of patients. Six patients (15.8%) died from unrelated causes. The signs and symptoms vary among duplications. Signs and symptoms leading to diagnosis and surgery varied according to the age of patient, location of the duplication, type of mucosal lining, duration of disease and presence of complication. The ideal surgical treatment of duplication is complete excision. However, the other treatment options should be well known.

摘要

消化道重复畸形是胃肠道系统罕见的异常情况之一。由于其体征和症状范围广泛,术前常难以做出诊断。熟悉其临床和手术特征有助于对重复畸形进行恰当的管理和治疗。我们进行了一项回顾性临床研究,以评估消化道重复畸形的临床和手术特征及治疗方法。在1971年至1997年的26年间,38例消化道重复畸形患者在哈杰泰佩大学儿科外科接受了手术。38例患者共发现42处重复畸形(男性20例,占53%;女性18例,占47%)。69%的患者在1岁前出现症状,24%在新生儿期出现症状。其中舌下1例,胸内9例(包括胸腹部2例),腹内32例。腹部肿块、腹胀、便秘、呕吐和呼吸窘迫是最常见的体征和症状。胸部和腹部平片、超声以及胸部和腹部计算机断层扫描是最常用的诊断性放射学检查方法。33处重复畸形(79%)呈球形,9处(21%)呈管状。2例患者(5.3%)出现多处重复畸形。14处重复畸形(33%)含有异位黏膜,大多为胃型。4处重复畸形(10%)在同一重复畸形中出现不止一种类型的异位黏膜。26%的患者伴有其他畸形。6例患者(15.8%)死于无关原因。不同的重复畸形其体征和症状有所不同。导致诊断和手术的体征和症状因患者年龄、重复畸形的位置、黏膜内衬类型、病程及并发症的存在而有所差异。重复畸形的理想手术治疗方法是完整切除。然而,其他治疗选择也应熟知。

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