成人先天性神经节巨结肠的治疗。

F Docobo Durántez, M Fernández Dovale, M Lozano Crivell, C Crivell Charneco
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引用次数: 0

摘要

本文报告5例12岁以上的先天性神经节性巨结肠。他们在西班牙塞维利亚“圣母Rocío”大学医院的消化系统服务和外科接受诊断和治疗。在描述了这种病理在幼儿期以外的罕见发病率后,对其诊断提出了不同的程序。一旦临床怀疑为巨结肠,应详细记录临床病史,特别参考出生时的排便习惯,并进行钡灌肠、肛肠测压、直肠内窥镜检查和活检进行组织学和组织化学研究。一旦确诊,所有患者都接受手术,包括切除腺体结直肠节段,将健康结肠直肠后降低,并通过内肛门括约肌纤维切除。健康结肠和病变直肠(Duhamel II)之间进行了侧对侧的经肛门吻合。所有患者均有满意的进展,几乎没有立即发病。术后5 ~ 10年,患者无症状,无排便习惯紊乱,发育正常。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Treatment of congenital aganglionic megacolon in adults].

The authors present 5 cases of congenital aganglionar megacolon in patients over 12 years of age. They were diagnosed and treated in the Digestive System Service and Surgery Department of the "Virgen del Rocío" University Hospital of Seville (Spain). After describing the infrequent incidence of this pathology outside early childhood, the different procedures proposed for its diagnosis are described. Once clinical suspicion of megacolon was established, a careful clinical history with special reference to bowel habit from birth was made, as well as a barium enema, anorectal manometry and rectal endoscopy and biopsy for histological and histochemical studies. Once diagnosed, all patients underwent surgery consisting in excision of the aganglionar colorectal segment, retrorectal lowering of the healthy colon and exteriorization through the fibers of the internal anal sphincter. A side-to-side transanal anastomosis between the healthy colon and diseased rectum (Duhamel II) was fashioned. All the patients had a satisfactory evolution with little immediate morbidity. Five to ten years after performing the operations, the patients remained asymptomatic, without bowel habit disturbances and showed an adequate development.

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