Congenital Scaphoid Megalourethra: A Case Report.

Urol Case Rep

Division of Urology, Department of Regenerative and Transplant Medicine, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

Published: September 2017

A congenital megalourethra is an enlargement of the pendulous urethra without evidence of distal obstruction. A 1-month-old boy presented to us with complaint of weak stream, ballooning of the penis before and during voiding and post voiding dribbling, since birth. Physical examination and cystourethroscope confirmed the diagnosis of congenital scaphoid megalourethra. He underwent reduction urethroplasty. During postoperative follow up, he had normal looking penis with good urinary stream.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458059PMC
http://dx.doi.org/10.1016/j.eucr.2017.05.002DOI Listing

Publication Analysis

Top Keywords

congenital scaphoid
8
scaphoid megalourethra
8
megalourethra case
4
case report
4
report congenital
4
congenital megalourethra
4
megalourethra enlargement
4
enlargement pendulous
4
pendulous urethra
4
urethra evidence
4

Similar Publications

Variations in the development of carpal bones are uncommon, with the scaphoid bone typically forming from the fusion of the os centrale carpi and the radial chondrification center during embryogenesis. A bipartite scaphoid is a rare congenital disorder that occurs when these ossification centers fail to fuse, with a prevalence ranging from 0.1% to 0.

View Article and Find Full Text PDF

We present the case of a 24-year-old man who sustained a scaphoid fracture in the presence of congenital scaphotrapezial and lunotriquetral coalitions. As the fracture progressed to a nonunion, a screw osteosynthesis was performed. The altered biomechanics caused by the two coalitions necessitated a dorso-proximal surgical approach, and two screws were implanted to prevent rotational instability.

View Article and Find Full Text PDF

Congenital megalourethra.

Ann Med Surg (Lond)

December 2022

Chief Division of Pediatric Surgery, Kabul University of Medical Science, Maiwand Teaching Hospital, Kabul, Afghanistan.

Background: Congenital megalourethra is a urogenital anomaly characterized by a cystic dilatation and elongation of the penile urethra resulting from the absence and hypoplasia of the corpus spongiosum and corpus cavernosum, or anterior urethral valve. There are two clinical types: scaphoid and fusiform. Generally, the etiology is unknown, but it is thought to be a defect in mesodermal development.

View Article and Find Full Text PDF

CONGENITAL SCAPHOID MEGALOURETHRA: REVISITING A RARE ANOMALY.

J Ayub Med Coll Abbottabad

February 2024

Department of Urology, Lady Reading Hospital, Peshawar, Pakistan.

Megalourethra is an infrequent malformation of the anterior urethra that is caused by the lack of corpus sponigosum and in severe cases is accompanied by the lack of corpora cavernosa as well. We report a five-year-old boy presented to us with scaphoid variety of megalourethra having complaints of ballooning of urethra during voiding. He was investigated with urethrogram and cystoscopy and subsequently repaired with Nesbitt Longitudinal Reduction Urethroplasty.

View Article and Find Full Text PDF

Nonsurgical Correction of Stahl's Ear in Neonates: A Case Study.

Plast Reconstr Surg Glob Open

October 2022

Plastic and Reconstructive Surgery Department, Nicosia General Hospital, Nicosia, Cyprus.

Stahl's ear deformity is a congenital auricular anomaly characterized by a third crus in the auricular cartilage, giving rise to an irregular helical rim and a bent scaphoid fossa. This deformity is mainly treated surgically during childhood. However, studies regarding ear-molding techniques show that postpartum splinting offers a safer and more effective permanent correction, and that happens because of the high circulating levels of estrogen that neonates receive from their mothers right after birth, making the cartilage more malleable.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!