Choledochal cyst is a rare congenital dilatation of the common bile duct usually symptomatic within the first year of life with rare presentation in adulthood. Herein, we present a 17-year-old female with type 1A choledochal cyst who was managed by surgical excision, hepatico-jejunostomy and jejunojejunostomy who recovered uneventfully.

Introduction: Cavernous hemangioma accounts for 0.6% of bladder tumors. We present a rare case Case Presentation: A 3-year-old girl presented with intravaginal swelling, dysuria, and hematuria. She received 26 cycles of VAC for embryonal rhabdomyosarcoma. Histopathology confirmed CH. Conclusion: CH should be considered in the differentials of childhood genitourinary masses.