Jul 2026· The Journal of medical research· Vol 12, pp. 109-112· 0 citations· 11 references
TL;DR
The case of a 44-year-old female who presented with lower urinary tract symptoms, including frequency, urgency, and a sensation of incomplete bladder emptying, underscores the importance of considering bladder leiomyoma in the differential diagnosis of bladder masses to avoid misinterpretation as a malignancy.
Abstract
Bladder leiomyoma is a rare benign mesenchymal tumor that can closely simulate malignant bladder lesions due to its nonspecific clinical and radiological features. Consequently, it often poses a diagnostic challenge. Here, we present a case of a 44-year-old female who presented with lower urinary tract symptoms, including frequency, urgency, and a sensation of incomplete bladder emptying. Imaging demonstrated a well-circumscribed mass arising from the right anterolateral wall of the urinary bladder. Transurethral resection was performed. Histopathological evaluation revealed a well-defined spindle cell tumor composed of intersecting fascicles of cytologically bland cells without atypia, mitotic activity, or necrosis. Immunohistochemistry showed diffuse positivity for smooth muscle actin and desmin with a low Ki-67 index, confirming the diagnosis of bladder leiomyoma. This case underscores the importance of considering bladder leiomyoma in the differential diagnosis of bladder masses to avoid misinterpretation as a malignancy. Accurate diagnosis relies on histopathological and immunohistochemical evaluation, and complete surgical excision ensures excellent clinical outcomes.
Abstract Background Primary leiomyosarcoma of the breast is an exceptionally rare mesenchymal tumor, constituting less than 1% of all breast malignancies. Its diagnosis is often delayed due to clinical and radiological similarities to more common benign or epithelial breast tumors. Case Presentation A 60-year-old woman...
Nishant Chopra, Abhishek Soni, Paramjeet Kaur et al.· Forum of Clinical Oncology· 0 citations
Primary large cell neuroendocrine carcinoma (LCNEC) of the bladder is an extremely rare and highly aggressive malignancy with a poor prognosis, bringing major challenges to clinical diagnosis and treatment. We report the case of a 77-year-old man who presented with recurrent gross hematuria for more than 8 months, acco...
Yu He, Hua-Zheng Kong, Cui-Juan-Cui Zhang et al.· Journal of Visualized Experi...· 0 citations
Epithelioid uterine leiomyoma is an uncommon histological variant and is exceptionally rare in adolescence. Its unusual anatomical presentation may complicate preoperative characterization, while definitive diagnosis relies on histopathological evaluation, including distinction from other uterine smooth muscle tu...
A. Cavallaro, Alessia Pagana, Sara Boemi et al.· BMC Women's Health· 0 citations
Background: Paraganglioma of the urinary bladder is a rare neuroendocrine tumor arising from chromaffin cells within the bladder wall. When functional, it may secrete catecholamines and present with characteristic symptoms such as hypertension, headache, palpitations, and sweating, which can be triggered by micturition...
O. Jendouzi, Lamghari Aziz, Aya Sobhi· Scholars Journal of Medical...· 0 citations
Uterine fibroids, also known as uterine leiomyomas, are common benign tumors in women of reproductive age, with a reported prevalence of 20–80 %. Vaginal leiomyoma is a rare smooth muscle tumor and up to date approximately 300 cases of vaginal leiomyomas have been described in the literature. The tumors are often asymp...
A. Mishina, L. S. Velenciuc, L. Sinitina et al.· Andrology and Genital Surger...· 0 citations
Primary vaginal leiomyomas are rare benign smooth muscle tumors that can pose a diagnostic challenge due to their unusual location and nonspecific presentation. We report a case of a female aged 29 years, on her routine checkup for primary infertility. On examination Incidental vaginal mass was found, a well-defined ma...
A. H. Pai, Madhurya Rudravadeyara Matada, Veena M. Vernekar et al.· International Journal of Rep...· 0 citations
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