Embryological Development of Persistent Cloaca. Hypothesis

Department of Pediatric Radiology of the 1-st State Hospital, Minsk, Belarus and Dorot. Medical Center for rehabilitation and geriatrics. Netanya. Israel

*Corresponding Author: Michael D Levin, MD, PhD, DSc, Department of Pediatric Radiology of the 1-st State Hospital, Minsk, Belarus & Dorot. Medical Center for rehabilitation and geriatrics, Netanya, Israel, Tel: 972-538281393, ORCID: 0000-0001-7830-1944, E-mail: [email protected]; [email protected]

Received Date: February 20, 2025

Published Date: March 04, 2025

Citation: Levin MD. (2025). Embryological Development of Persistent Cloaca. Hypothesis. Mathews J Surg. 8(1):37.

Copyrights: Levin MD. © (2025).

ABSTRACT

Introduction: While some authors suggest that anorectal malformations (ARMs) arise from abnormal development of the cloaca, only the true cloaca arises because of the cessation of the division of the cloaca stopping at the stage of development characteristic of female birds and reptiles. It is characterized by the confluence of the rectum, uterus, and bladder into a wide space, resulting in the complete absence of the urethra, vagina, and anal canal. Currently, following the articles by Hendren and Peña, persistent cloaca is the name given to the pathology that was previously called ARM with vaginal fistula. These patients have a urethra, vagina, and anal canal that supposedly merge into a common narrow channel. These patients are operated on as if they were patients with a true cloaca. Results: As a result of an analysis of literature and our own research, it has been shown that with all types of ARMs, except for the true cloaca, the pathology develops at a later embryonic period because of impaired development of the exodermal rudiment of the anal canal. By this time, normal development of the anal canal occurs up to the subcutaneous tissue. When the IAS does not encounter the ectodermal rudiment, as evidenced by the absence of the anus, it deviates forward and upward, forming a narrow, rigid fistula. This process leads to the ectopic positioning of the anus on the perineum, vestibule, urethra, or vagina. What surgeons typically remove during the pull-through procedure, under the guise of a fistula, is a functioning anal canal. A short, rigid fistula forms in the wall of the organ through which the IAS penetrates. Conclusion: Unlike a true cloaca, a persistent cloaca develops due to the penetration of the IAS through the vaginal wall before a cavity has formed within the vagina. As a result, the IAS creates a narrow long fistula that, in some cases, obstructs the emptying of the upper part of the vagina, leading to hydrocolpos. These patients typically have a normally functioning bladder and urethra, and in some cases, a functioning anal canal has been documented. Poor outcomes are the result of unnecessary and mutilating surgeries.

Keywords: Embryology Anorectal Malformations, Embryology Persistent Cloaca, Pathophysiology ARM, Diagnosis, Treatment, Hypothesis.