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Case Reports
. 2024 Feb 27:25:e942203.
doi: 10.12659/AJCR.942203.

Cloacal Dysgenesis Sequence in a Preterm Neonate

Affiliations
Case Reports

Cloacal Dysgenesis Sequence in a Preterm Neonate

Alexandra Vacaru et al. Am J Case Rep. .

Abstract

BACKGROUND Cloaca malformations result from a disproportion of apoptosis, cell growth, and maturation. The range of cloacal malformations is extensive and diverse, with a lack of a straightforward classification system. Cloacal dysgenesis sequence (CDS), also known as urorectal septum malformation sequence, is a rare cloaca variant described as the absence of a perineal orifice. Prenatal magnetic resonance imaging and antenatal ultrasounds may reveal a cloacal malformation; however, many patients are not diagnosed with cloacal malformation until birth. CASE REPORT We present a case of a female neonate delivered by a 23-year-old G2P1T1A0L0 mother who had received comprehensive prenatal care. During pregnancy, bilateral multicystic dysplastic kidneys were identified prenatally, leading to the in utero placement of a vesicoamniotic shunt. The physical exam revealed a distended abdomen with reduced abdominal musculature and laxity, ascites, a vesicoamniotic shunt in place, absent urethra, ambiguous genitalia with no vaginal opening, no perineal opening, and clubfoot. Abdominal radiograph showed findings consistent with significant abdominal ascites. An exploratory laparotomy was performed that included diverting colostomy, mucous fistula creation, tube vaginostomy, removal of the vesicoamniotic shunt, and suprapubic tube placement. The patient recovered well from this operation with no complications. CONCLUSIONS CDS is an uncommon condition in pediatric patients, and although sonographic findings can reveal urinary tract abnormalities, prenatal imaging might not always identify CDS. Our case underscores the uniqueness of the case and the significance of early detection and immediate medical and surgical intervention.

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Conflict of interest statement

Conflict of interest: None declared

Figures

Figure 1.
Figure 1.
Anorectal malformations, absent urethra, and absent vaginal opening, with ambiguous genitalia.
Figure 2.
Figure 2.
Preoperative abdominal radiograph demonstrating distended, gaseous loop of bowel in the midabdomen with a relative paucity of gas throughout the rest of the abdomen alongside a photograph taken at bedside.
Figure 3.
Figure 3.
Postoperative abdominal radiograph demonstrating resolution of bowel loops distension and evidence of distal gas extending through multiple loops of right hemiabdomen alongside photograph taken at bedside.

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