Urinary bladder cavernous hemangioma in a 3-year-old:
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Date
2022-04-26
Journal Title
Journal ISSN
Volume Title
Publisher
John Wiley & Sons Ltd.
Abstract
Cavernous hemangioma (CH) of urinary bladder occurs relatively infrequently,
accounting for 0.6% of all bladder tumors. This tumor may occur sporadically
or coexist with other benign and malignant vascular lesions. In this report, we
present a rare case of CH in a 3-year-old Ugandan girl. A 3-year-old girl was re ferred to Mbarara Regional Referral Hospital (MRRH) for urological evaluation
following a 3-year history of intravaginal swelling, dysuria, and heavy hematuria
resulting in anemia. Imaging was consistent with polypoid bladder mass arising
from the bladdertrigone. Embryonalrhabdomyosarcoma wassuspected based on
clinical eyeballing. She was worked up for chemotherapy and received 26 cycles
of vincristine sulfate, actinomycin-d, and cyclophosphamide (VAC). Biopsy and
fulguration were performed after optimizing the patient. Histopathology con firmed CH. The surgery was uneventful and resulted in complete cure. CH should
be considered in the differential diagnosis of childhood genitourinary masses. It
is a rare entity in the real-life clinical practice and therefore can be overlooked.
Excision biopsy and histology should be performed before initiating the patients
to chemotherapy. CH is very insensitive to chemotherapy and therefore surgery
maybe adequate in resource-limited settings.
Description
Keywords
cavernous hemangioma, embryonal rhabdomyosarcoma
Citation
Odongo CN, Atwine R, Kirya F, et al. Urinary bladder cavernous hemangioma in a 3-year-old: A rare case report. Clin Case Rep. 2022;10:e05875. doi:10.1002/ccr3.5875