Results 81 to 90 of about 356 (134)
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Exstrophy of the Bladder

Neonatal Network, 1999
Exstrophy of the bladder is a rare congenital defect that occurs when the abdominal wall and underlying structures, including the ventral wall of the bladder, fail to fuse in utero. As a result, the lower urinary tract is exposed, and the everted bladder appears through the abdominal opening.
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The repair of exstrophy of the bladder

British Journal of Plastic Surgery, 1978
OVER the last IO years, 25 patients with exstrophy of the bladder have been treated at this centre. Many had received initial surgical treatment elsewhere and were referred for correction of remaining deformities. Usually no attempt had been made to reconstruct the abdominal wall and pubic area by adequate transposition of skin nor to correct the ...
J C, van der Meulen, G G, Thomas
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Carcinoma in exstrophy of the bladder

The American Journal of Surgery, 1948
T HIRTY cases of carcinoma occurring in the exstrophic bladder have been reported in the literature. We wish to report an additional case, making a total of thirty-one reported cases. McCown l6 summarized the reported cases of exstraphy of the bladder in 1gqo and added one case, bringing the number of reported cases up to twenty-five.
W C, REID, G W, WESTCOTT, J E, SUMMERS
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Female bladder exstrophy

International Urogynecology Journal, 1997
Bladder exstrophy is one of the most challenging congenital urinary tract abnormalities. Apart from the open bladder the patient also has various other abnormalities, including urogenital, musculoskeletal and anorectal defects. The size of the exstrophic bladder varies from patient to patient.
S J, Crankson, S, Ahmed
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Hypospadias and bladder exstrophy

Current Opinion in Urology, 2002
Reconstructive surgery for patients with hypospadias, bladder exstrophy and cloacal exstrophy is challenging. Over the last few years, more and more data have become available concerning incidence and epidemiology, as well as short- and long-term results of surgical techniques.
Raimund, Stein, Joachim W, Thüroff
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Duplicate exstrophy of the bladder

Journal of Pediatric Surgery, 1999
Duplicate exstrophy of the bladder is a rare, distinct congenital anomaly without additional major anomalies of the urinary tract. A 15-year-old boy with duplicate exstrophy is reported on, and the possible role of bladder sequestration in the development of classical musculoskeletal deformities in this anomaly is discussed.
F, Andiran, F C, Tanyel
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Ureterosigmoidostomy in Bladder Exstrophy

European Urology, 1983
Experience with ureterosigmoidostomy (US) using a reflux prevention technique in 38 of 48 cases of bladder exstrophy is reviewed. During a follow-up period of 14 years, the results were excellent as to morphological changes of the upper urinary tract, incontinence, psychological development and social behavior.
D H, Frohneberg   +2 more
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Bladder Reconstruction in Exstrophy

Journal of Urology, 1980
Between 1968 and 1978, 35 patients with complete exstrophy of the bladder have been treated. In 31 cases reconstruction was attempted using a 3-step procedure. First, the bladder was closed with a posterior iliac osteotomy and in the male patient the penis was lengthened. Next, an antireflux procedure and bladder neck reconstruction were done.
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An Unusual Bladder/Cloacal Exstrophy with Urachal Exstrophy

Urologia Internationalis, 2008
The authors report a previously unpublished association of bladder exstrophy with cleft lip, exomphalos, Meckel’s diverticulum imperforate anus, and a large urachal mass protruding below the umbilicus. The baby underwent surgical repair of the condition and the postoperative recovery was uneventful.
George, Sakellaris   +2 more
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Rectal Bladder in the Treatment of Bladder Exstrophy

European Urology, 1979
Satisfactory results were obtained in 25 patients with bladder exstrophy treated by the Heitz-Boyer-Hovelacque operation.
U, Bracci, C, Laurenti
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