• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
A STUDY OF THE VESICAL GANGLIA IN CHILDREN AND THE RELATIONSHIP TO THE MEGAURETER MEGACYSTIS SYNDROME AND HIRSCHSPRUNG'S DISEASE.儿童膀胱神经节及其与巨输尿管巨膀胱综合征和先天性巨结肠关系的研究
J Clin Pathol. 1963 Jul;16(4):342-50. doi: 10.1136/jcp.16.4.342.
2
Megacolon in an adult case of hypoganglionosis, a pseudo-Hirschsprung's disease: an autopsy study.成人低神经节症(一种假性先天性巨结肠)中的巨结肠:一项尸检研究
Intern Med. 2008;47(5):421-5. doi: 10.2169/internalmedicine.47.0275. Epub 2008 Mar 3.
3
The incidence and outcome of allied disorders of Hirschsprung's disease in Japan: Results from a nationwide survey.日本先天性巨结肠相关疾病的发病率及转归:一项全国性调查结果
Asian J Surg. 2017 Jan;40(1):29-34. doi: 10.1016/j.asjsur.2015.04.004. Epub 2015 Jul 26.
4
Vesical gigantism or congenital megacystis.膀胱巨大症或先天性巨膀胱。
Urology. 1984 Dec;24(6):601-3. doi: 10.1016/0090-4295(84)90111-0.
5
Japanese clinical practice guidelines for allied disorders of Hirschsprung's disease, 2017.《2017年日本先天性巨结肠相关疾病临床实践指南》
Pediatr Int. 2018 May;60(5):400-410. doi: 10.1111/ped.13559.
6
ROENTGENOLOGIC MANIFESTATIONS OF HIRSCHSPRUNG'S DISEASE IN INFANCY.婴儿期先天性巨结肠的X线表现
Am J Roentgenol Radium Ther Nucl Med. 1965 Sep;95:217-29. doi: 10.2214/ajr.95.1.217.
7
Classification and diagnostic criteria of variants of Hirschsprung's disease.先天性巨结肠症变异型的分类与诊断标准。
Pediatr Surg Int. 2013 Sep;29(9):855-72. doi: 10.1007/s00383-013-3351-3.
8
[Congenital megaureter and its implications].[先天性巨输尿管及其影响]
Urologe A. 1982 Nov;21(6):312-7.
9
Megacystis, megacolon, and malrotation: a new syndromic association?巨膀胱-巨结肠-内脏转位综合征:一种新的综合征关联?
Am J Med Genet A. 2011 Aug;155A(8):1798-802. doi: 10.1002/ajmg.a.34119. Epub 2011 Jul 7.
10
Unfavorable outcome in a child with megaureter-megacystis syndrome complicated by mild acute poststreptococcal glomerulonephritis.
Pediatr Int. 2010 Dec;52(6):895-6. doi: 10.1111/j.1442-200X.2010.03272.x.

引用本文的文献

1
Hirschsprung's disease.先天性巨结肠
Postgrad Med J. 1967 Mar;43(497):135-40. doi: 10.1136/pgmj.43.497.135.
2
Constipation in infants and children.婴幼儿便秘
Gut. 1971 Jan;12(1):85-90. doi: 10.1136/gut.12.1.85.
3
The application of studies in vitro to the management of Hirschsprung's disease and of megacolon in adults.体外研究在成人先天性巨结肠症和巨结肠症治疗中的应用。
Am J Dig Dis. 1968 May;13(5):434-42. doi: 10.1007/BF02233665.
4
A vascular cause for aganglionic bowel. A new hypothesis.无神经节性肠管的血管病因。一种新假说。
Am J Dig Dis. 1972 Mar;17(3):255-61. doi: 10.1007/BF02232298.

本文引用的文献

1
Megaloureter; new concept in treatment.巨输尿管;治疗的新概念。
South Med J. 1952 Mar;45(3):171-6.
2
A new concept of the etiology of megaloureters.巨输尿管病因的新概念。
N Engl J Med. 1952 Jan 10;246(2):41-6. doi: 10.1056/NEJM195201102460201.
3
Hirschsprung's disease.先天性巨结肠症
Lancet. 1951 Feb 10;1(6650):302-9. doi: 10.1016/s0140-6736(51)92290-8.
4
Atony of the female bladder; report of four cases.女性膀胱无张力;4例报告
Br Med J. 1959 Jan 17;1(5115):149-51. doi: 10.1136/bmj.1.5115.149.
5
Congenital abnormalities of intestinal innervation; absence of innervation of jejunum, ileum and colon in siblings.
Pediatrics. 1958 Feb;21(2):261-6.
6
Cine-radiology of congenital bladder-neck obstruction and the megaureter.先天性膀胱颈梗阻与巨输尿管的影像放射学
Br J Urol. 1957 Dec;29(4):410-5. doi: 10.1111/j.1464-410x.1957.tb09374.x.
7
Some observations on the pathology of congenital idiopathic bladder-neck obstruction (Marion's disease).关于先天性特发性膀胱颈梗阻(马里恩病)病理学的一些观察
Br J Urol. 1957 Dec;29(4):393-8. doi: 10.1111/j.1464-410x.1957.tb09371.x.
8
Aganglionic megacolon, pheochromocytoma, megaloureter, and neurofibroma; co-occurrence of several neural abnormalities.
AMA J Dis Child. 1957 Aug;94(2):185-91. doi: 10.1001/archpedi.1957.04030030079012.
9
[The role of the peripheral autonomic nervous system in the pathogenesis of acquired dystonic bladders (megacystis)].[外周自主神经系统在后天性张力障碍性膀胱(巨膀胱)发病机制中的作用]
Z Urol. 1956;49(4):197-207.
10
The relation of megacolon and megaloureter.巨结肠与巨输尿管的关系。
N Engl J Med. 1955 Dec 29;253(26):1147-50. doi: 10.1056/NEJM195512292532603.

儿童膀胱神经节及其与巨输尿管巨膀胱综合征和先天性巨结肠关系的研究

A STUDY OF THE VESICAL GANGLIA IN CHILDREN AND THE RELATIONSHIP TO THE MEGAURETER MEGACYSTIS SYNDROME AND HIRSCHSPRUNG'S DISEASE.

作者信息

LEIBOWITZ S, BODIAN M

出版信息

J Clin Pathol. 1963 Jul;16(4):342-50. doi: 10.1136/jcp.16.4.342.

DOI:10.1136/jcp.16.4.342
PMID:14044036
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC480575/
Abstract

A method for the assay of vesical ganglion cells is described and the number and distribution of the neurones in three normal bladders was studied. Vesical ganglion counts were done in cases of the megaureter-megacystis syndrome, megaureter, bladder neck obstruction, megacystis associated with absent abdominal muscles, Hirschsprung's disease, and lumbar myelomeningocoele. A normal complement of neurones was found in each case. No evidence was found that the megaureter-megacystis syndrome is due to an agenesis of the peripheral autonomic ganglia similar to that in Hirschsprung's disease. Vesical ganglia were normal in the two cases examined and no clinical association was found between the two conditions in a large series of cases. Moreover, a study of the cell counts suggests that at least some of the reports of such a lesion are based upon an inadequate appreciation of the number and distribution of neurones in the normal urinary tract.

摘要

本文描述了一种检测膀胱神经节细胞的方法,并研究了三个正常膀胱中神经元的数量和分布。对巨输尿管-巨膀胱综合征、巨输尿管、膀胱颈梗阻、伴有腹肌缺如的巨膀胱、先天性巨结肠和腰骶部脊髓脊膜膨出病例进行了膀胱神经节计数。在每个病例中均发现神经元数量正常。未发现证据表明巨输尿管-巨膀胱综合征是由于外周自主神经节发育不全所致,与先天性巨结肠类似。在所检查的两个病例中,膀胱神经节正常,在大量病例中未发现这两种情况之间存在临床关联。此外,细胞计数研究表明,至少一些关于这种病变的报告是基于对正常尿路中神经元数量和分布的认识不足。