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基于肝脏三维重建对婴儿型肝肾多囊病分类的评论

Comments upon the classification of infantile polycystic diseases of the liver and kidney, based upon three-dimensional reconstruction of the liver.

作者信息

Adams C M, Danks D M, Campbell P E

出版信息

J Med Genet. 1974 Sep;11(3):234-43. doi: 10.1136/jmg.11.3.234.

DOI:10.1136/jmg.11.3.234
PMID:4431029
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1013132/
Abstract

Three-dimensional reconstructions of portal tracts of two babies with different forms of infantile polycystic disease of the kidney and liver, and of a child with congenital hepatic fibrosis, have shown important differences between these three conditions. A strong plea is made for the application of this technique, and of microdissection of kidneys, to a large series of cases in order to develop a valid classification of these conditions.

摘要

对两名患有不同类型肝肾婴儿型多囊病的婴儿以及一名患有先天性肝纤维化的儿童的门管区进行三维重建,结果显示这三种病症之间存在重要差异。强烈呼吁将这项技术以及肾脏显微解剖技术应用于大量病例,以便对这些病症建立有效的分类。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e09b/1013132/ef9b41703940/jmedgene00320-0021-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e09b/1013132/409718ce1481/jmedgene00320-0015-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e09b/1013132/b3e39ad0a942/jmedgene00320-0017-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e09b/1013132/b5d688f948c0/jmedgene00320-0017-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e09b/1013132/63627211f771/jmedgene00320-0018-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e09b/1013132/4664d0dee066/jmedgene00320-0020-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e09b/1013132/8c5ec05acb7b/jmedgene00320-0020-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e09b/1013132/f42a987252a0/jmedgene00320-0021-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e09b/1013132/ef9b41703940/jmedgene00320-0021-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e09b/1013132/409718ce1481/jmedgene00320-0015-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e09b/1013132/b3e39ad0a942/jmedgene00320-0017-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e09b/1013132/b5d688f948c0/jmedgene00320-0017-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e09b/1013132/63627211f771/jmedgene00320-0018-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e09b/1013132/4664d0dee066/jmedgene00320-0020-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e09b/1013132/8c5ec05acb7b/jmedgene00320-0020-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e09b/1013132/f42a987252a0/jmedgene00320-0021-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e09b/1013132/ef9b41703940/jmedgene00320-0021-b.jpg

相似文献

1
Comments upon the classification of infantile polycystic diseases of the liver and kidney, based upon three-dimensional reconstruction of the liver.基于肝脏三维重建对婴儿型肝肾多囊病分类的评论
J Med Genet. 1974 Sep;11(3):234-43. doi: 10.1136/jmg.11.3.234.
2
Polycystic disease of kidney and liver presenting in childhood.儿童期出现的肝肾多囊病。
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[HEPATO-RENAL POLYCYSTIC DISEASES].
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Phenotypic correlates of autosomal recessive (infantile) polycystic disease of kidney and liver: criteria for classification and genetic counseling.常染色体隐性(婴儿型)肝肾多囊病的表型关联:分类及遗传咨询标准
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High-resolution three-dimensional visualization of hepatic sinusoids in cirrhotic rats via serial histological sections.通过连续组织切片实现肝硬化大鼠肝窦的高分辨率三维可视化。
Histol Histopathol. 2021 May;36(5):577-586. doi: 10.14670/HH-18-339. Epub 2021 Apr 14.
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A pedigree study of perinatally lethal renal disease.围生期致死性肾病的系谱研究。

本文引用的文献

1
PATHOGENESIS OF POLYCYSTIC KIDNEYS. SURVEY OF RESULTS OF MICRODISSECTION.多囊肾的发病机制。显微切割结果综述。
Arch Pathol. 1964 May;77:510-2.
2
Congenital hepatic fibrosis.先天性肝纤维化
Q J Med. 1961 Jan;30:91-117.
3
Familial dysplasia of kidneys, liver and pancreas: a probably genetically determined syndrome.家族性肾、肝和胰腺发育异常:一种可能由基因决定的综合征。
J Med Genet. 1985 Apr;22(2):104-11. doi: 10.1136/jmg.22.2.104.
4
Meckel's syndrome (dysencephalia splanchno-cystica) in two Pakistani sibs.两名巴基斯坦同胞中的梅克尔综合征(内脏囊肿性脑发育不全)
J Med Genet. 1978 Jun;15(3):242-5. doi: 10.1136/jmg.15.3.242.
Acta Paediatr (Stockh). 1959 Jan;48(1):1-11. doi: 10.1111/j.1651-2227.1959.tb16011.x.
4
Cysts arising in the renal tubules. A microdissection study.肾小管源性囊肿。一项显微解剖研究。
Arch Dis Child. 1965 Oct;40(213):464-73. doi: 10.1136/adc.40.213.464.
5
Cystic diseases of the kidney--radiological and pathological considerations.
Clin Radiol. 1969 Jan;20(1):65-82. doi: 10.1016/s0009-9260(69)80061-9.
6
A case of abnormal intrahepatic bile duct arrangement submitted to three dimensional reconstruction.一例肝内胆管排列异常的病例接受了三维重建。
Acta Pathol Microbiol Scand A. 1971;79(3):303-6.
7
Polycystic disease of kidney and liver presenting in childhood.儿童期出现的肝肾多囊病。
J Med Genet. 1971 Sep;8(3):257-84. doi: 10.1136/jmg.8.3.257.