Bladder exstrophy is a urogenital malformation characterized by an abnormality of the cloacal membrane that forms the intra-umbilical abdominal wall during the first weeks of embryonic life.

It presents itself under 3 aspects: the classical form or complete vesical extrophy, the partial form which is rare and the extended form known as extrophy of the cloaca also very rare [1] [2] [3].

In Africa, the presence of an apparent malformation is often interpreted as a curse or the result of witchcraft.

In addition, there are also socio-economic factors and the lack of qualified medical personnel in peripheral health facilities with the result that pregnant women cannot properly follow their pregnancies in a health facility in order to detect possible malformation in time during the antenatal period

Bladder exstrophy, diagnosed during the morphological examination in the 2nd trimester of pregnancy may be a reason for voluntary termination of pregnancy [4] [5].

Bladder exstrophy is a rare pathology; its frequency is estimated at 1 in 10,000 to 50,000 births [6].

It affects about one in 40,000 infants according to the Boston Children’s Hospital in the United States of America [5].

We report the clinical case of a newborn having a complete bladder exstrophy received and treated in our hospital and make a review of the literature.

It was a 21-month-old male child who had been referred to us from a rural health center on the outskirts of Bamenda in North West Region of Cameroon.

At birth, the malformation was obvious and after several unsuccessful consultations in health facilities in the region, he was sent to us for management

The study of his antecedents had revealed that he was the last born in family of three and no malformation had been revealed in his brothers. Similarly, there was no concept of consanguinity between the parents. No ultrasound examination documented the pregnancy follow-up of the mother, who said that she had done her prenatal consultations correctly.

The clinical examination revealed a conscious child in good general condition with normal reflexes.

At the hypogastric level, the presence of a reddish plate was noted with the presence of the two ureteral orifices measuring 11 cm long axis each through which intermittently flowed urine associated with the absence of the dorsal face of the penis (Figure 1). There was also a diastasis of the right muscles in the lower abdominal wall, a displaced navel. The examination expanded to other organs did not reveal other apparent malformations.

The renal blood test was normal with serum creatinine at 5 mg/L and there was no urinary infection on the cyto-bacteriological examination of the urine. The abdominal and pelvic ultrasound did not visualize the bladder because of acoustic window and there was no renal dilation.

In order to obtain a reservoir, a primary surgical closure of the exstrophy and epispadia associated with reconstruction of the anterior abdominal wall without osteotomy was performed. The patient was seen at 3 months with a micturition jet but we could not judge the urinary continence because at this age the child does not yet have micturition autonomy (Figure 2). It was planned a control at 6 months, 1 year, and 5 years but the appointment was not respected.

Exstrophy of the bladder is a birth defect. It is a rare malformation that affects about one in 40,000 infants according to the Boston Children’s Hospital [6].

Exstrophy of the bladder is an apparent malformation discovered at birth. In our case the patient was consulted after 21 months of birth with a bladder dry and retracted.

In developed countries, this pathology is diagnosed during the antenatal life and this intervention is carried out, ideally at 24 - 48 after birth.

The clinical examination of our patient revealed: a diastasis of the straight muscles in the lower abdominal wall, a displaced navel, an inflammatory bladder plate and an associated penile epispadia.

In the literature, in addition to the clinical data of our patient, there is often a diastasis of the associated pubis and in the girl a short urethra, extended labia and a narrow vaginal opening [6] [7]. We did not observe any diastasis of pubic bones in our patient who had good walking.

The work up (urea and blood creatinine, cytobacteriological examination of the urine, radiography of the pelvis and ultrasound of the urinary system) were to check urinary infection, signs of renal insufficiency and the presence of other associated malformations.

Therapeutically, two positions are opposed in the literature:

The first consists of primary closure of the bladder and urethral plate, reconstruction of the lower abdominal wall, and approximation of the pubic bones with or without osteotomy. This has the advantage that it realizes a bladder tank early enough, thus ensuring good healing of the bladder plate and good recovery of continence later. However, it has the disadvantage of being a heavy surgery at this age requiring a long anesthesia, and traumatizes the children.

The other approach is to correct the malformation by successive interventions carried out at different ages of the child:

· Closure of the bladder and urethral plate and reconstruction of the lower abdominal wall at first leaving the child with epispadia and incontinence at maximum 48 hours of birth,

· Correction of the epispadia at 6 months after hormonal stimulation in a second time and

· Surgery for the incontinence and vesical-kidney reflux at 4 - 5 years of age [8] [9].

In our case, the patient’s non-compliance with appointments did not reveal the possibility of performing an enlargement cystoplasty or an uretero-vesical reimplantation.

In any case, taking into account the parents’ expectations and the psychosocial discomfort that this malformation may cause in the child, this surgery must be performed at best by a qualified surgeon with a certain experience in the field and with equipment adapted to this type of surgery, which is not always the case in some African countries [5].

In our case, despite the fact that it was a 21-month-old child, the operative follow-ups were a success, particularly the repair of the bladder and the urethra as first-line treatment.

The long-term follow-up of our patient would have allowed us to judge the opportunity to perform an ureterovesical reimplantation. The latter, however, is almost always indicated because the majority of these children still have vesico-renal reflux, which can lead to a deterioration of renal function [8].

Bladder exstrophy is an apparent malformation that can be diagnosed on prenatal ultrasound in the first trimester and can lead to pregnancy termination in countries with low skills.

When diagnosed at birth, well-managed surgical management can give a good morpho-functional result.

The authors declare no conflicts of interest regarding the publication of this paper.

Demba, C., Mamadou II, B., Daouda, K., Ibrahima, B., Diawo, B.M., Oury, D.T.M., Bissiriou, B.M., Houssein, F., Edwin, F., Sama, C.M., Ab, D. and Raphiou, B.O. (2019) Management of Bladder Exstrophy: A Case Report in the Urological Ward at Saint Elizabeth General Catholic Hospital SHISONG. Open Journal of Urology, 9, 162-166. https://doi.org/10.4236/oju.2019.910019