Epispadias: Difference between revisions
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== Epispadias == | |||
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Revision as of 22:07, 16 February 2025
Epispadias is a rare type of malformation of the penis in males or the urethra in females that is present at birth. This condition is characterized by the abnormal location of the urethra, the tube that drains urine from the body.
Overview
In males with epispadias, the urethra generally opens on the top or side of the penis rather than the tip. However, it can also be present along the entire length of the penis. In females, the urethral opening can be located in the abdomen or the area between the clitoris and the labia.
Causes
Epispadias is caused by a malfunction during the early stages of pregnancy. The exact reason for this malfunction is not known, but it is believed to be related to improper development of the pubic bone. In many cases, epispadias is associated with bladder exstrophy, a condition in which the bladder is turned inside out and exposed on the outside of the abdomen.
Symptoms
The symptoms of epispadias can vary greatly depending on the severity of the condition. Some common symptoms include a wide, short penis with an abnormal curvature, a small, open bladder, and urinary incontinence.
Diagnosis
Epispadias is usually diagnosed at birth by a physical examination. Additional tests may be performed to determine the severity of the condition and to check for any associated abnormalities. These tests may include a ultrasound, a cystoscopy, or a voiding cystourethrogram.
Treatment
The treatment for epispadias usually involves surgery to correct the position of the urethral opening and, in males, to straighten the penis. In some cases, additional surgery may be needed to manage urinary incontinence. The goal of treatment is to improve the appearance and function of the genitalia and to achieve urinary and fecal continence.


