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消化道重复畸形。临床特征、首选治疗方法及相关畸形。

Duplications of the alimentary tract. Clinical characteristics, preferred treatment, and associated malformations.

作者信息

Ildstad S T, Tollerud D J, Weiss R G, Ryan D P, McGowan M A, Martin L W

机构信息

Department of Pediatric Surgery, Children's Hospital Medical Center, Cincinnati, OH 45229.

出版信息

Ann Surg. 1988 Aug;208(2):184-9. doi: 10.1097/00000658-198808000-00009.

Abstract

Duplications of the alimentary tract are unusual congenital anomalies that frequently present a diagnostic as well as therapeutic challenge to the surgeon. Because these lesions occur so infrequently, they are often not suspected until encountered intraoperatively. Due to the complicated anatomy and common blood supply shared between the duplication and associated native bowel, appropriate management requires a familiarity with the anatomy and clinical characteristics of this entity. To better define the range of patient characteristics, clinical presentation, and preferred therapy, 20 enteric duplications were reviewed in 17 patients treated at the Children's Hospital Medical Center from 1956 to 1986. Ages of patients ranged from 1 day to 11 years; 60% were less than 2 years of age at initial presentation. Seven duplications in six patients involved alimentary tract structures of foregut derivation (esophagus, stomach, and Parts I and II of duodenum), with a predominance of girls (4 of 6). Most of these patients (67%) presented with moderate to severe acute respiratory distress and a mass present on chest radiograph. In 67% of the patients, the correct diagnosis was established before operation. None required emergency operative intervention. By contrast, 13 duplications in 11 patients were of midgut or hindgut derivation (Parts III and IV of the duodenum, jejunum, ileum, and colon). In this group of patients, 62% of the duplications involved the cecum, 23% involved the ileum, and 16%, the jejunum. Seventy-eight per cent of the patients were boys. The most common symptoms were nausea and vomiting, and the most common sign was a palpable abdominal mass. Emergency operative intervention was required of eight of 11 patients with duplications involving the small bowel and colon. Three patients presented with an intussusception, four with signs and symptoms consistent with acute appendicitis, one with a small bowel obstruction, and two with gastrointestinal hemorrhage due to the presence of ectopic gastric mucosa within the duplication. It was found that two important points must be considered in regard to the management of enteric duplications: (1) the common blood supply shared between the duplication and native bowel must be carefully protected to avoid undue sacrifice of normal bowel, and (2) the presence of heterotopic gastric mucosa in 35% of patients negates internal drainage.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

消化道重复畸形是一种罕见的先天性异常,常常给外科医生带来诊断和治疗上的挑战。由于这些病变极为少见,往往直到术中才被怀疑。由于重复畸形与相关正常肠管之间解剖结构复杂且血供相同,恰当的处理需要熟悉该病症的解剖结构和临床特征。为了更好地明确患者特征、临床表现及首选治疗方法的范围,我们回顾了1956年至1986年在儿童医院医疗中心接受治疗的17例患者中的20例肠道重复畸形病例。患者年龄从1天至11岁不等;60%的患者初诊时年龄小于2岁。6例患者中的7处重复畸形累及前肠来源的消化道结构(食管、胃以及十二指肠的第一和第二部分),其中女孩居多(6例中的4例)。这些患者大多数(67%)表现为中度至重度急性呼吸窘迫,胸部X线片显示有肿块。67%的患者在手术前确诊。均无需紧急手术干预。相比之下,11例患者中的13处重复畸形为中肠或后肠来源(十二指肠的第三和第四部分、空肠、回肠和结肠)。在这组患者中,62%的重复畸形累及盲肠,23%累及回肠,16%累及空肠。78%的患者为男孩。最常见的症状是恶心和呕吐,最常见的体征是可触及的腹部肿块。11例累及小肠和结肠的重复畸形患者中有8例需要紧急手术干预。3例患者表现为肠套叠,4例有与急性阑尾炎相符的体征和症状,1例有小肠梗阻,2例因重复畸形内存在异位胃黏膜而出现胃肠道出血。研究发现,在肠道重复畸形的处理方面必须考虑两个要点:(1)必须小心保护重复畸形与正常肠管之间共享的血供,避免过度牺牲正常肠管;(2)35%的患者存在异位胃黏膜,这使得内引流不可行。(摘要截选至400字)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/838c/1493602/e3caccd44a1f/annsurg00186-0086-a.jpg

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