1997
DOI: 10.1016/s0022-5347(01)64910-3
|View full text |Cite
|
Sign up to set email alerts
|

Structural Changes of Collagen Components and Diminution of Nerves in Congenital Ureteropelvic Junction Obstruction

Abstract: In the intrinsic obstruction, nerve fibers were depleted in the muscular layers in the ureteric walls, resulting in dysfunction and atrophy of muscle fibers and an increase of collagen fibers in the muscle layers with abnormal accumulation of intercellular and interstitial collagen. These changes may disrupt the mobility of UPJ and lead to both mechanical and functional obstruction.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

2
41
1
3

Year Published

2000
2000
2020
2020

Publication Types

Select...
5
4
1

Relationship

0
10

Authors

Journals

citations
Cited by 90 publications
(47 citation statements)
references
References 18 publications
2
41
1
3
Order By: Relevance
“…There are many explanations for the decrease in the extension ability of the narrow segments, which lead to the functional discontinuity of ureteropelvic muscle contractions: disorders in muscular structure, atrophy or a decrease in the number of smooth muscle cells, a decrease in the number of ICC and nerve endings, and an increase in the collagen deposits between the muscular clusters. 16,17 Some researchers consider the intrinsic function disorder as the underlying mechanism of the obstruction, and suggest that morphologic changes are secondary. 18 Pacemaker cells which demonstrate spontaneous depolarization and are electrically associated with ureteral smooth muscle cells are required for pyeloureteral peristalsis.…”
Section: Discussionmentioning
confidence: 99%
“…There are many explanations for the decrease in the extension ability of the narrow segments, which lead to the functional discontinuity of ureteropelvic muscle contractions: disorders in muscular structure, atrophy or a decrease in the number of smooth muscle cells, a decrease in the number of ICC and nerve endings, and an increase in the collagen deposits between the muscular clusters. 16,17 Some researchers consider the intrinsic function disorder as the underlying mechanism of the obstruction, and suggest that morphologic changes are secondary. 18 Pacemaker cells which demonstrate spontaneous depolarization and are electrically associated with ureteral smooth muscle cells are required for pyeloureteral peristalsis.…”
Section: Discussionmentioning
confidence: 99%
“…The renal phenotype of ADAMTS-1 -/-mice resembles human ureteropelvic junction obstruction, which is the most common cause of congenital hydronephrosis and is recognized in nearly 1 in 500 live births (27). This disease is characterized by abnormal collagen and smooth muscle components at the ureteropelvic junction that contribute to mechanical or functional obstruction of urinary flow (27,28). Interestingly, the structural abnormalities in ADAMTS-1 -/-mice are responsible for the same dysfunctions described in cases of congenital ureteropelvic junction obstruction and primary obstructive megaureter in humans (29,30).…”
Section: Figurementioning
confidence: 99%
“…Murakumo et al emphasized the importance of a multifaceted approach combining neurogenic and myogenic theories in understanding the etiopathogenesis of intrinsic UPJ obstruction (13). A recent non-invasive study, which focused on the measuring urinary TGF-β 1 in children with congenital UPJ obstruction confi rmed this urinary cytokine as a useful tool for the diagnosis and follow-up of UPJ obstruction (14).…”
Section: Discussionmentioning
confidence: 99%