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直肠吸引活检中乙酰胆碱酯酶活性检测对肠道神经节发育异常诊断的研究:单中心17年经验

Study of acetylcholinesterase activity in rectal suction biopsy for diagnosis of intestinal dysganglionoses: 17-year experience of a single center.

作者信息

Santos Maria Mercês, Tannuri Uenis, Coelho Maria Cecília M

机构信息

Pediatric Surgery Laboratory (LIM 30), University of São Paulo Medical School, São Paulo, Brazil.

出版信息

Pediatr Surg Int. 2008 Jun;24(6):715-9. doi: 10.1007/s00383-008-2141-9. Epub 2008 Apr 12.

Abstract

Although the utility of the acetylcholinesterase (AChE) histochemistry on rectal suction biopsy in diagnosing Hirschsprung's disease (HD) has been documented, few reports address a great number of biopsies and patients. Our aim is to present a 17-year experience on the method of rectal suction biopsy and AChE histochemical staining for diagnosis of intestinal dysganglionoses. Between August 1989 and July 2006, 297 children suspected of having HD were submitted to rectal suction biopsies that were evaluated by the same two surgeons. There were 18 complications (6.0%), namely one self-limited rectal bleeding and 17 (5.7%) inadequate procedures that were repeated. A total of 157 patients (52.8%) showed no increased AChE activity and the remaining patients (140-47.2.0%) presented patterns of increased AChE activity confirming the diagnosis of HD or neuronal intestinal dysplasia. Among the 140 cases suspected as having HD, in 131 children the diagnosis of HD was confirmed and they were operated on. The histological studies showed that 111 children presented the classic form of HD or a long spastic segment. Sixteen children presented total colonic aganglionosis and four children proved to have intestinal neuronal dysplasia, according to histological and radiological criteria. Nine (6.6%) newborns were identified as false-positives and no false-negative results were verified. The rectal suction biopsy combined with AChE staining is advantageous for the differentiation between normal bowel and intestinal dysganglionoses. The rectal suction method is simple and can easily be performed by experienced surgeons. The histological evaluation is very objective and can be performed by a non-pathologist.

摘要

尽管直肠吸引活检中乙酰胆碱酯酶(AChE)组织化学在诊断先天性巨结肠(HD)中的效用已有文献记载,但很少有报告涉及大量活检和患者。我们的目的是介绍17年来直肠吸引活检及AChE组织化学染色诊断肠道神经节发育异常的经验。1989年8月至2006年7月,297名疑似患有HD的儿童接受了直肠吸引活检,由同两位外科医生进行评估。共有18例并发症(6.0%),即1例自限性直肠出血和17例(5.7%)活检不充分而进行了重复操作。总共157例患者(52.8%)AChE活性未升高,其余患者(140例,47.2%)AChE活性升高,确诊为HD或神经元性肠发育异常。在140例疑似HD的病例中,131例儿童确诊为HD并接受了手术。组织学研究表明,111例儿童呈现HD的经典形式或长痉挛段。16例儿童表现为全结肠无神经节细胞症,4例儿童根据组织学和放射学标准被证实患有肠道神经元发育异常。9例(6.6%)新生儿被确定为假阳性,未发现假阴性结果。直肠吸引活检联合AChE染色有利于区分正常肠管和肠道神经节发育异常。直肠吸引方法简单,经验丰富的外科医生易于操作。组织学评估非常客观,非病理学家也可进行。

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