IntroductionCloacal exstrophy (CE) is an exceedingly rare and complex congenital defect that involves the exstrophy of the urinary, gastrointestinal, and genital organs, with an estimated incidence of less than 1 in 200,000 live births [1]. It is widely considered one of the most severe and complicated anomalies in pediatric urology and surgery, given the involvement of multiple organ systems [2]. Typically, CE is associated with other malformations, including myelomeningocele, imperforate anus, and omphalocele, and it poses significant challenges to both diagnosis and management [3]. The condition results from a failure in normal embryologic development of the cloaca, a structure that, during the early stages of gestation, separates into the urogenital sinus and the anorectal canal. When this separation process is disrupted before the fourth week of gestation, it leads to the manifestation of CE [4].Historically, the prognosis for children born with cloacal exstrophy was poor, with survival rates hindered by associated complications such as sepsis, short bowel syndrome, and renal failure [5]. However, advances in neonatal care, surgical techniques, and post-operative management have significantly improved survival rates in recent decades, with current survival rates ranging from 83% to 100% in some regions [6]. The complexity of CE requires a multidisciplinary approach, often involving pediatric surgeons, urologists, and other specialists to address the various associated defects [7]. Traditionally, the surgical management of CE was approached in multiple stages, beginning with the creation of an ileostomy, followed by bladder closure, abdominal wall repair, and other reconstructive procedures [8]. However, with the advent of improved techniques, primary repair strategies are now being explored and implemented with promising results in carefully selected cases [9].Despite these advancements, long-term outcomes remain variable, and many challenges still exist in achieving functional outcomes such as urinary and fecal continence, as well as addressing the cosmetic and psychological aspects of care [10]. The current treatment approach emphasizes individualized care, addressing the most life-threatening conditions initially while progressively managing the anatomical and functional restoration of affected organs [11]. This case report aims to highlight a successful example of primary repair for cloacal exstrophy, including the closure of the posterior bladder wall and the creation of an ileostomy, with an emphasis on the current progress and challenges in the management of this complex condition.