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Updated: Nov 1, 2025

An Orthotopic Model of Murine Bladder Cancer

An Orthotopic Model of Murine Bladder Cancer

Published on: February 6, 2011

Haemangiomas in the urinary bladder: Two case reports.

Gui-Cheng Zhao¹, Chang-Xing Ke²

¹Department of Urology, The Second Affiliated Hospital of Kunming Medical University, Kunming 650101, Yunnan Province, China.

World Journal of Clinical Cases

|June 18, 2021

Summary

This summary is machine-generated.

Urinary bladder haemangioma is a rare benign tumor in young patients. Diagnosis requires histopathology, and treatment varies, with surgery offering favorable outcomes.

Keywords:

Case report Haemangioma Haematuria Urinary bladder

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Area of Science:

Urology
Pediatric Oncology
Surgical Pathology

Background:

Urinary bladder haemangioma is a rare, benign, nonurothelial tumor predominantly affecting pediatric and adolescent populations.
Standard clinical and radiological assessments are often insufficient for accurate diagnosis of this condition.
This case series aims to increase awareness and guide appropriate management strategies for urinary bladder haemangioma.

Observation:

Two pediatric cases of urinary bladder haemangioma were diagnosed via histopathology and immunohistochemistry.
Surgical interventions included radical cystectomy with ileal conduit diversion (Case 1) and laparoscopic partial cystectomy (Case 2).
Both cases demonstrated successful resolution of hematuria post-surgery.

Findings:

Histopathology and immunohistochemistry are crucial for accurate diagnosis of urinary bladder haemangioma.
Surgical management, tailored to individual cases, led to favorable outcomes in both reported instances.
No recurrence was observed during 3-year follow-up for Case 1 and 3-month follow-up for Case 2.

Implications:

Accurate diagnosis of urinary bladder haemangioma relies on detailed histopathological and immunohistochemical analysis.
While no gold standard treatment exists, surgical options provide effective management for urinary bladder haemangioma.
Early diagnosis and appropriate surgical intervention can lead to favorable long-term prognoses for pediatric patients.