Mullerianosis of the Urinary Bladder: A Rare Case Report

Authors

  • Richa Bhartiya Grant Government Medical College, Mumbai, India
  • Pallavi Mehra Patna Medical College, Patna, Bihar, India
  • Vishal Tayade Grant Government Medical College, Mumbai, India
  • Navin Kumar Bariar Patna Medical College, Patna, Bihar, India

DOI:

https://doi.org/10.21276/apalm.3688

Keywords:

müllerianosis, endocervicosis, endometriosis, endosalpingosis, case report

Abstract

Endocervicosis, endometriosis, and endosalpingosis are choristomas derived from Müllerian tissue, collectively termed Müllerianosis. We report a 40-year-old woman with pelvic pain and dysuria who presented with a 3.2×2.5 cm bladder mass four years post-hysterectomy. Transurethral resection revealed endocervical glands and endometrial stroma deep in the bladder wall. Immunohistochemistry confirmed ER/PR positivity in glandular epithelium and CD10 positivity in stroma, establishing the diagnosis of Müllerianosis. Outcome: The patient remained asymptomatic with no recurrence over 8 years of clinical and cystoscopic follow-up. Müllerianosis is a rare benign bladder lesion that can mimic malignancy. Accurate histopathological diagnosis with immunohistochemistry is essential to avoid unnecessary radical surgery and enable hormonal therapy when indicated.

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Published

06-02-2026

Issue

Section

Case Report / Case Series

How to Cite

1.
Mullerianosis of the Urinary Bladder: A Rare Case Report. Ann of Pathol and Lab Med [Internet]. 2026 Feb. 6 [cited 2026 Feb. 11];13(2):C73-C76. Available from: https://pacificejournals.com/journal/index.php/apalm/article/view/3688