Bladder polyps in cloacal exstrophy: A histological series

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Cloacal Exstrophy Repair with Primary Closure of Bladder Exstrophy: A Case Report and Review of Literature

Cloacal exstrophy is the most complex congenital, ventral, abdominal wall defect. Traditionally surgery consists of a staged approach to repair which takes place on many separate theatre visits. In this case a primary approach was undertaken resulting in a relatively short inpatient stay and a reduced risk from multiple surgical procedures under general anaesthesia.

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Cloacal exstrophy: a complex disease.

INTRODUCTION Cloacal exstrophy is a rare occurrence with an incidence of 1:200,000 to 1:400,000 live births. It represents one of the most challenging reconstructive endeavors faced by pediatric surgeons and urologists. Aside from the genitourinary defects, there are other associated anomalies of the gastrointestinal, musculoskeletal and neurological systems that require a multidisciplinary app...

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Cloacal Exstrophy: A Histomorphological Analysis of the Bladder Plate and Correlation with Bladder Dynamics

Objective: Physiological outcomes in patients of cloacal exstrophy are governed primarily by neurological innervation and detrusor histomorphology. An evaluation of the bladder plate histomorphology for the presence of neural elements, collagen fibres and smooth muscle components was done and correlation attempted with detrusor physiology. Methods: From three cases of cloacal exstrophy, full th...

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Y chromosome aberration in a patient with cloacal-bladder exstrophy-epispadias complex: an unusual finding.

Chromosome aberrations or genetic syndromes associated with cloacal-bladder exstrophy complex have rarely been reported. The aim of this report is to describe a 14 year-old female Brazilian patient with a complex urogenital malformation, short stature, lack of secondary se-xual characteristics and Y chromosome aberration. A girl with cloacal bladder exstrophy complex was referred for evaluation...

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Urea salvage in a neonate with cloacal exstrophy.

Urea kinetics were measured in a child with congenital absence of the colon on days 15, 19, and 23 of age. Urea salvage was 5% of urea production in the first study, increasing to 79% by the third. This provides evidence that the colonic microflora play a more active part in urea salvage than the mucosa and that the establishment of an active lower ileal microflora takes over some of the metabo...

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ژورنال

عنوان ژورنال: Journal of Pediatric Surgery Case Reports

سال: 2018

ISSN: 2213-5766

DOI: 10.1016/j.epsc.2017.12.005