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Bladder glandular cystitis causing renal dysfunction: A case report.
Salim Lachkar1, Ahmed Ibrahimi1, Imad Boualaoui1
1Department of Urology A, Ibn Sina University Hospital, Rabat, Morocco.
International Journal of Surgery Case Reports
|March 24, 2025
Summary
Glandular cystitis (GC) is a rare bladder condition that can mimic tumors. Early diagnosis via histopathology and markers like CK7/CK20 is crucial for management and surveillance due to potential malignancy.
Area of Science:
- Urology
- Oncology
- Pathology
Background:
- Glandular cystitis (GC) is a rare bladder condition characterized by urothelial metaplasia, often associated with chronic irritation.
- It can mimic malignant bladder tumors, necessitating accurate histopathological diagnosis using markers such as CK7 and CK20.
- While typically benign, GC carries a risk of co-existing carcinoma, mandating long-term patient surveillance.
Observation:
- A 68-year-old active smoker presented with symptoms of acute kidney injury, flank pain, and urinary issues.
- Imaging revealed bilateral hydronephrosis and a significant bladder lesion.
- Histopathology confirmed intestinal glandular cystitis after transurethral resection.
Findings:
- The patient experienced symptom relief and improved quality of life following treatment and stabilization.
- Three-year surveillance cystoscopies showed no recurrence of the glandular cystitis.
- Diagnosis was confirmed using cystoscopy, histopathology, and immunohistochemical markers.
Implications:
- Glandular cystitis requires prompt recognition and diagnosis to guide appropriate management strategies.
- Vigilant follow-up is essential due to the potential for malignant transformation in some cases.
- This case highlights the importance of tailored management and ongoing care for rare bladder conditions like GC.
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