2006
DOI: 10.1111/j.1464-410x.2006.06420.x
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Congenital urethral obstruction: the video‐endoscopic perspective

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Cited by 7 publications
(7 citation statements)
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“…Compared with prenatal diagnoses or severe infant cases associated with renal/upper urinary tract disorders, however, no consensus has been reached with regard to the importance of relatively mild urethral lesions detected after the onset of urinary symptoms or urinary tract infection in school‐age children as the underlying disease or even with regard to a specific term for this condition. Congenital urethral obstructions reported so far include PUV types 1 to 3 [7], COPUM [8–10], Cobb’s collar [11], Moormann’s ring [12], mini‐valve, congenital bulbar urethral narrowing [13,14] and syringocoele (Cowper’s gland cyst) [15,16]. Agreement has been reached that type 2 PUV is overclassified by Young and does not actually exist [17].…”
Section: Discussionmentioning
confidence: 99%
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“…Compared with prenatal diagnoses or severe infant cases associated with renal/upper urinary tract disorders, however, no consensus has been reached with regard to the importance of relatively mild urethral lesions detected after the onset of urinary symptoms or urinary tract infection in school‐age children as the underlying disease or even with regard to a specific term for this condition. Congenital urethral obstructions reported so far include PUV types 1 to 3 [7], COPUM [8–10], Cobb’s collar [11], Moormann’s ring [12], mini‐valve, congenital bulbar urethral narrowing [13,14] and syringocoele (Cowper’s gland cyst) [15,16]. Agreement has been reached that type 2 PUV is overclassified by Young and does not actually exist [17].…”
Section: Discussionmentioning
confidence: 99%
“…An 8.5‐F or 11.5‐F endoscope (Wolf) was cautiously inserted into the urethra so as not to miss even minor urethral lesions. Congenital urethral obstructive lesions were not classified by Young’s classification [7], but based on the fact that obstruction mainly results from membranous lesions extending down from the anterior urethral wall rather than valvular lesions of PUV, they were classified as follows: congenital obstructive posterior urethral membrane (COPUM) [8–10], which is primarily characterized by membranous lesions projecting from the anterior urethral wall (12 o’clock direction) located in the posterior urethra and connecting with the verumontanum in the 6 o’clock direction (similar to type 1 PUV; Fig. 1A,B); and Cobb’s collar [11], which is characterized by an all‐round septum located at the bulbomembranous junction that does not connect with the verumontanum (similar to type 3 PUV and Moormann’s ring [12]) (Fig.…”
Section: Methodsmentioning
confidence: 99%
“…This, however, may not directly correlate with the degree of obstruction seen on direct endoscope evaluation. 6 It has been shown that patients can be successfully treated with cold knife incision or electrical cautery. The latter is associated with submucosal thermal injury and the development of de novo urethral strictures.…”
Section: Discussionmentioning
confidence: 99%
“…It has been well documented that even in children with clinically and endoscopically significant PUV, the VCUG picture may be extremely variable. It is not uncommon to find an endoscopically severe PUV with only minimal or moderate posterior urethral dilatation on the VCUG, with a low initial urethral ratio, thus requiring a high index of suspicion to diagnose urethral obstruction [3,4]. In such cases, it is unlikely that urethral ratio would be useful either to diagnose or to test the adequacy of treatment.…”
mentioning
confidence: 95%