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上尿路的囊性扩张:放射科医生的发育模型。

Cystic dilatations of the upper urinary tract: a radiologist's developmental model.

作者信息

Mellins H Z

出版信息

Radiology. 1984 Nov;153(2):291-301. doi: 10.1148/radiology.153.2.6435168.

DOI:10.1148/radiology.153.2.6435168
PMID:6435168
Abstract

The ureteral bud in the embryonic kidney grows and branches dichotomously for 15 generations. This branching tree is modified by a series of narrowings and expansions and becomes the ureter, the renal pelvis, the calyces, and the collecting tubules. Simultaneously, the ureteral bud induces the formation of nephrons. If many of the renal cystic diseases and congenital dilatations of the renal pelvis and ureter are viewed as a series of growth disturbances along the branching ureteral bud, their morphology and pathophysiology become clarified even though their etiology is often not known.

摘要

胚胎肾中的输尿管芽生长并进行二叉状分支达15代。这一分支树通过一系列变窄和扩张而发生改变,进而成为输尿管、肾盂、肾盏和集合小管。同时,输尿管芽诱导肾单位的形成。如果将许多肾囊性疾病以及肾盂和输尿管的先天性扩张视为沿分支输尿管芽发生的一系列生长紊乱,那么即便其病因往往不明,它们的形态学和病理生理学也会变得清晰明了。

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1
Cystic dilatations of the upper urinary tract: a radiologist's developmental model.上尿路的囊性扩张:放射科医生的发育模型。
Radiology. 1984 Nov;153(2):291-301. doi: 10.1148/radiology.153.2.6435168.
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Medullary sponge kidney presenting as polycystic renal disease.表现为多囊肾病的髓质海绵肾。
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[Medullary sponge kidney with megapyelon and primary congenital megaureter in unilateral renal aplasia].[单侧肾发育不全合并巨肾盂及原发性先天性巨输尿管的髓质海绵肾]
Fortschr Geb Rontgenstr Nuklearmed. 1969 Jul;111(1):137-40.
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Extrarenal calyces: a rare anomaly of the renal collecting system.肾外肾盏:一种罕见的肾集合系统异常。
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Renal branching morphogenesis: morphogenetic and signaling mechanisms.肾分支形态发生:形态发生和信号传导机制。
Semin Cell Dev Biol. 2014 Dec;36:2-12. doi: 10.1016/j.semcdb.2014.07.011. Epub 2014 Jul 28.
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Simultaneous medullary sponge and adult polycystic kidney disease: the need for accurate diagnosis.髓质海绵肾与成人多囊肾病并存:准确诊断的必要性。
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[Congenital anomalies of the kidney and ureter].[肾脏和输尿管的先天性异常]
Acta Chir Iugosl. 1975;22(1 Suppl):257-62.
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[Obstructive malformations of the urinary tract: prenatal diagnosis].[泌尿系统梗阻性畸形:产前诊断]
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Congenital polycystic kidneys associated with hydroureters and atresia of lower urinary tract in a stillborn infant.死产婴儿中先天性多囊肾合并输尿管积水及下尿路闭锁
N Y State J Med. 1953 Nov 1;53(21):2519-21.

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