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短结肠
相关语句
  short colon
     Conclusions Congenital anorectal malformation associated with short colon is scarce with a low incidence of12.5%(2/16). This disease was divided into IV types.
     结论先天性肛门直肠畸形伴短结肠较罕见,本组发生率为12.5%(2/16)。
短句来源
     Association of Imperforate Anus with Short Colon (AIASC):diagnosis and treatment
     肛门闭锁短结肠联合征的诊断和治疗
短句来源
     Preliminary surgery is colostomy at the short colon site in infancy and definitive surgical repair is undertaken when infant age exceeded3~6months.
     新生儿期在短结肠处造瘘,待3~6个月后行根治术。
短句来源
     Methods Autopsies of sixteen cases of congenital anorectal malformation were made and2cases of anorectal deformity associated with short colon was found. Anatomicohistologic examinations were used to observe the pathomorphologic changes.
     方法对16例先天性肛门直肠畸形行尸检,发现2例有肛门直肠畸形合并短结肠,行解剖组织学方法观察。
短句来源
     To assess the experience of diagnosis and treatment of Association of Imperforate Anus with Short Colon in children.
     探讨肛门闭锁短结肠联合征诊治中的若干问题。
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  相似匹配句对
     Association of Imperforate Anus with Short Colon (AIASC):diagnosis and treatment
     肛门闭锁结肠联合征的诊断和治疗
短句来源
     The articles are short.
     文章 ;
短句来源
     Promotion of Colonic Adaptation for Short Bowel Rat by Diet Fiber and Enteral Nutrition Treatment
     膳食纤维促肠大鼠结肠代偿
短句来源
     gubernaculum short.
     引带
短句来源
     Management of Patients with Colon Injury
     结肠损伤的处理
短句来源
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  short colon
Congenital short colon with imperforate anus (pouch colon)
      
It was found to consist of a long oesophagus, a two-chambered stomach, a small intestine measuring only 5.2×body length, two rudimentary caeca and a short colon, typical of carnivorous birds.
      
Imperforate anus with congenital short colon (pouch colon syndrome)
      
There have not been many case reports of imperforate anus with congenital short colon (pouch colon syndrome).
      
Imperforate anus with congenital short colon: combined abdominal and posterior sagittal approach
      
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To assess the experience of diagnosis and treatment of Association of Imperforate Anus with Short Colon in children.Methods From May, 1986 to May, 1998. 14 children (male 6.female 8) with AIASC were reviewed. It was found that the blood supply of one side of short colon in 12 patients was from the inferior mesenteric vessels, they were treated by 1-stage or 2-stage coloplasty (to reform the saccular colon in to Tubular one) and anoplasty procedure (by overding the muscle ular cuff of the stump of colon to form...

To assess the experience of diagnosis and treatment of Association of Imperforate Anus with Short Colon in children.Methods From May, 1986 to May, 1998. 14 children (male 6.female 8) with AIASC were reviewed. It was found that the blood supply of one side of short colon in 12 patients was from the inferior mesenteric vessels, they were treated by 1-stage or 2-stage coloplasty (to reform the saccular colon in to Tubular one) and anoplasty procedure (by overding the muscle ular cuff of the stump of colon to form an internal sphincter).Results Seven cases of 13 were alive (54 % ). Among 7 operated newborn patients. 2 were alive (28. 6% ). 5 of six infants patients, were alive (83% ). All of the 7 living cases were followedup 1-12 years (mean 7. 3 years). One died of unrelated disease. and six cases were living well.Conclusions Earlier diagnosis and colostomy in newborn, and tubular coloplasty plus internal sphineter plastic procedure in infants are important in improving the cure rate and reducing the mortality of AIASC.

探讨肛门闭锁短结肠联合征诊治中的若干问题。方法作者对1986年5月以后诊断治疗的14例患儿的临床资料进行回顾性分析,观察发现12例患儿存在肠乐膜下血管,并对其采用了短结肠的管状成形术和袖套状翻转结肠肌层的肛门成形术。结果手术病人7/13(54%)存活,新生儿2/7(28.6%)存活,幼儿患者5/6(83%)存活。新生儿病人,术式未改进前病人死亡率高,效果差。幼儿及术式改良后死亡率明显下降,效果明显改善。结论及时正确诊断,新生儿期结肠造口、幼儿期行短结肠管状成形及末端肌层袖状翻转肛门成形术能明显改善患儿预后。

Objective To explore the pathology of congenital anorectal malformation associated with short colon malformation.Methods Autopsies of sixteen cases of congenital anorectal malformation were made and2cases of anorectal deformity associated with short colon was found.Anatomicohistologic examinations were used to observe the pathomorphologic changes.Results The two cases with short colon malformation were both males and high anus atresia.The distal rectums dilated extremely and the thickness of intestinal walls...

Objective To explore the pathology of congenital anorectal malformation associated with short colon malformation.Methods Autopsies of sixteen cases of congenital anorectal malformation were made and2cases of anorectal deformity associated with short colon was found.Anatomicohistologic examinations were used to observe the pathomorphologic changes.Results The two cases with short colon malformation were both males and high anus atresia.The distal rectums dilated extremely and the thickness of intestinal walls were only1/2~1/4of the normal intestines,which belonges to type I.Under microscopic observation,the nerve plexuses and ganglions in intermuscular and submucous layers were scarce.Conclusions Congenital anorectal malformation associated with short colon is scarce with a low incidence of12.5%(2/16).This disease was divided into IV types.In the group of the patients with high anus atresia accompanied by short colon without fistula,short colon dilated extremely;intestinal walls was very thin;the development was postponed;there were few nerve plexuses and ganglions in intermuscular and submucous layers.Other group of the patients with anus atresia associated with bladder fistula,urethral fistula or vaginal fistula,short colon might have peristaltic function.The intestines were edema ,hyperemia or have ulceration.In intermuscular and submucous layers,there might be nerve plexuses and ganglions,and its change were normal,reduced or deficient.This disease could be diagnosed through X-ray examination before operations.Preliminary surgery is colostomy at the short colon site in infancy and definitive surgical repair is undertaken when infant age exceeded3~6months.

目的探讨先天性肛门直肠畸形伴短结肠的病理。方法对16例先天性肛门直肠畸形行尸检,发现2例有肛门直肠畸形合并短结肠,行解剖组织学方法观察。结果2例均为男性,高位无肛伴短结肠。直肠盲端极度扩张,壁薄如纸,仅为正常肠壁的1/2~1/4,属Ι型。镜下,肌间和粘膜下神经丛和神经节细胞极少。结论先天性肛门直肠畸形伴短结肠较罕见,本组发生率为12.5%(2/16)。高位无肛伴短结肠、无瘘者,短结肠极度扩张,壁菲薄如纸,肠壁各层发育薄弱,肌间和粘膜下神经丛和神经节细胞极少。无肛畸形合并膀胱瘘、尿道瘘、阴道瘘者,短结肠可有蠕动功能,肠壁全层肥厚水肿,粘膜充血及溃疡,粘膜下层和肌间可能有神经丛和神经节细胞,其改变可为正常、减少或缺如。术前经X线摄片或造影确诊。新生儿期在短结肠处造瘘,待3~6个月后行根治术。

 
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