A case of hypospadias in a dog
© The Author(s) 2005
Published: 1 September 2005
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© The Author(s) 2005
Published: 1 September 2005
This clinical case report described a three-month-old mongrel dog that had the urethral orifice opening 3 cm from the tip of the penis and lacked a completely formed preputial sheath. It was presented to the clinic with an exposed penile shaft that was dry. The dog had urinary incontinence that was not of neurological origin. It also had unilateral agenesis of the right testicle. The preputial sheath was successfully reconstructed. Urinary incontinence stopped soon after surgery, suggesting that it had been probably due to an ascending urethritis. A large preputial opening was left because of the location of the urethral opening.
Hypospadias is a congenital developmental anomaly of the external genitalia in male animals  and man , in which the external urethral orifice is on the ventral surface of the penis rather than at the tip of the glans. To a variable extent in individual cases, there is failure of fusion of the urogenital folds and incomplete development of the penile urethra [8, 6]. The urethra may open at any level on the ventral surface of the penis somewhere between the normal location and the ischiatic arch or on the surface of the perineum [8, 11]. In severe cases, lesions such as failure of the two halves of the scrotum to fuse, underdevelopment or absence of the penis, and failure of the urethra to close in the perineal area may be seen [7, 13, 1, 14]. The urethral meatus may be located along the scrotal raphe . In one report  hypospadias was seen in association with unilateral renal agenesis, whilst in another report there was underdevelopment of the penis, fusion failure of the urethra, prepuce and scrotum. Other abnormalities associated with hypospadias are retained testicles, bone or anorectal defects, umbilical hernia, hydrocephalus, and urinary incontinence [5, 10].
There are relatively few reports of this condition in the veterinary literature but this may not reflect the true prevalence of the condition . Its aetiology is unclear ; it may be due to inadequate production of androgens by the foetal testes or to inadequate numbers of androgen receptors on the urethral folds.
This case report describes a three-month-old mongrel dog that had hypospadias, unilateral retained testicle, urinary incontinence, and absence of a fully formed preputial sheath which has not been described before.
This report describes a case of hypospadias in a three-month-old dog with an incompletely formed preputial sheath. The cause of hypospadias is not known; it is thought that the affected foetus may secrete inadequate quantities of testosterone or that there may be inadequate conversion of testosterone to dihydrotestosterone in the target tissues of the urogenital sinus and external genitalia [11, 12]. The severity of defects present depends on the degree of androgen insufficiency. A spectrum occurs from mild hypospadias, in which the urinary orifice is located in the glans penis to severe hypospadias where the orifice is at the penoscrotal junction, scrotum, or the perineum [8, 11, 1]. In the dog, exposure of the male foetus to progesterone or anti-androgens during gestation, especially between day 30 and day 44 of pregnancy, may be responsible . Severe genetic defects including cryptorchidism , absence of the scrotum, bifid scrotum , and persistent müllerian structures have been observed in dogs. In many cases in animals and man, chromosome analysis can be used to differentiate hypospadias from true hermaphroditism .
Surgical correction is usually not attempted because the urethra cranial to the abnormal orifice is deficient. In the present case although the uretheral opening was 3 cm from the tip of the penis, it was patent up to the urinary bladder. One author  unsuccessfully attempted to reconstruct the urethra and, subsequently carried out amputation of the penis whilst others [13, 3] recommended the removal of the open prepuce, partial penile amputation and prescrotal or perineal urethrostomy and castration as the treatment for hypospadias. When there are severe urethral defects, excision of the external genitalia and urethrostomy is the treatment of choice . In the present case the preputial sheath was easily reconstructed to cover the exposed penis. It was not necessary to modify the preputial orifice since, after surgery, the preputial opening created was sufficiently large and long enough to allow outflow of urine without scalding the ventral abdominal skin.
It is thought that initially the penis appeared dry because of exposure to the air and it was soiled whenever the dog lay down. This must have caused irritation and probable ascending urethritis from bacteria entering through the abnormally located urethral opening. Urinary incontinence without neurological deficits is a frequent observation in dogs with hypospadias. In the present case it is presumed that the constant penile irritation and ascending urethritis could have been responsible for the urinary incontinence. In some animals penile and preputial disorders may be associated with pain, incontinence or reluctance to breed. In the present case, the owner was not interested in breeding the dog, and was satisfied with the outcome of surgery. It is concluded that in the less severe cases of hypospadias an attempt should be made to surgically reconstruct the affected parts. Although the cause of hypospadias is not known, affected dogs should not be used for breeding purposes.
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