Male Cloaca: A Rare Case Report

Authors

• Md Nazrul IslamConsultant, Department of Pediatric Surgery, Bangabandhu Sheikh Mujib Medical University
• Talima AkterAssistant Professor, Department of Microbiology, Holy Family Red Crescent Medical College
• Pravin ChaudharyResident, Department of Pediatric Surgery, Bangabandhu Sheikh Mujib Medical University
• Md Ruhul AminProfessor, Department of Pediatric Surgery, Bangabandhu Sheikh Mujib Medical University
• A S M Shahidul HossainConsultant, Radiology & Imaging Department, Bangabandhu Sheikh Mujib Medical University
• Mohammad Mahabubul AlamAssistant Professor, Department of Pediatric Surgery, Cumilla Medical College, Cumilla.

Keywords

Abstract

Cloacal malformation is a rare condition that usually referred only to females. We are reporting a very rare case of cloacal malformation variant in a 6-years-old boy who presented with absent anal opening along with hypospadiac penis with chordee with passage of urine and stool from an abnormal opening in the penoscrotal region.

Journal of Paediatric Surgeons of Bangladesh (2025) Vol. 13 (1 & 2): 52–53