Male cloaca: A rare case report

Authors

  • Md Nazrul Islam Consultant, Department of Pediatric Surgery Bangabandhu Sheikh Mujib Medical University
  • Talima Akter Assistant Professor, Department of Microbiology Holy Family Red Crescent Medical College
  • Pravin Chaudhary Resident, Department of Pediatric Surgery Bangabandhu Sheikh Mujib Medical University
  • Md Ruhul Amin Professor, Department of Pediatric Surgery Bangabandhu Sheikh Mujib Medical University
  • A S M Shahidul Hossain Consultant Radiology & Imaging department Bangabandhu Sheikh Mujib Medical University
  • Mohammad Mahabubul Alam Assistant Professor, Department of Pediatric Surgery Cumilla Medical College, Cumilla.

DOI:

https://doi.org/10.3329/jpsb.v13i1.87418

Keywords:

cloaca, ARM, rectourethral fistula, proximal hypospadias

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 (2022) Vol. 13 (1 & 2): 52-53

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Published

2026-01-31

How to Cite

Islam, M. N., Akter, T., Chaudhary, P., Amin, M. R., Hossain, A. S. M. S., & Alam, M. M. (2026). Male cloaca: A rare case report. Journal of Paediatric Surgeons of Bangladesh, 13(1), 52–53. https://doi.org/10.3329/jpsb.v13i1.87418

Issue

Vol. 13 No.1-2 (2022)

Section

Case Reports

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