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1.
Urology ; 192: e107-e109, 2024 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-38906267

RESUMEN

Fibroepithelial polyps in the urinary tract are a rare cause of obstructive uropathy with fewer than 130 cases reported in the literature. In our series, we describe polyps that were missed on preoperative imaging and later found in the operating room during pyeloplasty. It is critical for urologists to be aware of polyps as a potential source of obstruction as they can increase the complexity of a reconstruction and, if missed, may result in a failed repair and persistent obstruction. We hypothesize that performing a retrograde pyelogram prior to ureteric reconstruction will facilitate diagnosis prior to surgical repair.


Asunto(s)
Pólipos , Obstrucción Ureteral , Humanos , Pólipos/cirugía , Pólipos/diagnóstico , Masculino , Femenino , Obstrucción Ureteral/cirugía , Obstrucción Ureteral/etiología , Obstrucción Ureteral/diagnóstico , Neoplasias Ureterales/diagnóstico , Neoplasias Ureterales/cirugía , Neoplasias Ureterales/patología , Persona de Mediana Edad , Adulto
2.
Urology ; 166: 223-226, 2022 08.
Artículo en Inglés | MEDLINE | ID: mdl-35461916

RESUMEN

OBJECTIVE: To report on our experience performing office-based pediatric urologic procedures. We hypothesize that office-based interventions are safe and effective for children, avoiding unnecessary risk and cost associated with general anesthesia. METHODS: We retrospectively identified patients undergoing office-based interventions from 2014 to 2019, including lysis of penile or labial adhesions, division of skin bridges, meatotomy and excision of benign lesion. Success was defined as a completed attempt in the office. Failure includes any unsuccessful office attempts. Complications include 30-day ED visits/readmissions and recurrent skin bridge post division of skin bridge. RESULTS: We identified 1326 interventions: 491 lyses of penile adhesions (37%), 320 division of skin bridges (24%), 128 lyses of labial adhesions (10%), 348 meatotomies (26%), and 39 excisions of benign lesions (3%) [Table 1]. There was a >95% success rate reported in every procedure with an overall complication rate of 0.6%. Excision of benign lesion had 100% success rate. ED visits within 30 days are rare (0.2%), and no patients required admission after their procedure [Table 2]. The rate of recurrence was highest following lysis of labial adhesions (13.3%). Of the 54 patients who underwent retreatment, very few required general anesthesia (n = 6). CONCLUSION: Office-based urologic interventions in children are well tolerated with excellent safety and efficacy. Complications and recurrence are universally low. Ultimately, 99.5% of this cohort was managed under local anesthetics, thereby avoiding the risks of anesthesia use in the pediatric population.


Asunto(s)
Procedimientos Quirúrgicos Ambulatorios , Anestésicos Locales , Procedimientos Quirúrgicos Ambulatorios/métodos , Anestesia General , Niño , Estudios de Cohortes , Humanos , Estudios Retrospectivos
3.
Urology ; 144: 260, 2020 10.
Artículo en Inglés | MEDLINE | ID: mdl-32988492
4.
Urology ; 100: 224-227, 2017 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-27614119

RESUMEN

Beckwith-Wiedemann Syndrome (BWS) is an overgrowth disorder with various congenital anomalies. Although the most classic constellation includes macrosomia, macroglossia, and omphalocele, nephrourological findings are commonly associated with BWS. Clinical presentation is highly variable because of its complex molecular heterogeneity, which involves changes in DNA methylation and disruption of growth regulatory genes. We report 3 pediatric patients, ages 13 months to 3 years old, who presented with clinical features consistent with BWS. A variety of nephrourological abnormalities were also noted, including posterior urethral valves, hydroureteronephrosis, and undescended testes. Genetic testing for all 3 patients revealed duplication of the region chromosome 11p15.5.


Asunto(s)
Síndrome de Beckwith-Wiedemann/diagnóstico , Síndrome de Beckwith-Wiedemann/genética , Duplicación Cromosómica , Cromosomas Humanos Par 11 , Síndrome de Beckwith-Wiedemann/diagnóstico por imagen , Preescolar , Humanos , Lactante , Masculino
5.
Urology ; 97: 170-171, 2016 11.
Artículo en Inglés | MEDLINE | ID: mdl-27561849
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