Genital arteriovenous malformations are rare and present unique surgical challenges in preserving urogenital function, abdominal wall integrity, and lower limb perfusion. A 32-year-old man with a giant abdominoscrotal arteriovenous malformation presented with recurrent heavy bleeding. Due to the high risk of rebleeding and fatal hemorrhage, surgery with curative intent was proposed and the patient was counseled on the risks of ischemia to the lower limb, testes, and penis. Preoperative embolization of the feeding vessels was performed. Three days later, surgical excision of the mass with the affected scrotum, left rectus muscle, sheath, and overlying abdominal skin followed. The testes were dissected from the malformation and preserved along with the right internal pudendal artery. The left thigh skin was advanced to the scrotal remnants and a neoscrotum created. The resulting large abdominal wall defect was reconstructed in layers with a pedicled anterolateral thigh flap, including innervated vastus lateralis muscle, to prevent herniation. Recovery was uneventful, and a 4-year follow-up revealed no significant clinical or radiological recurrence with recovery of flap sensation, retained erectile function, and no herniation. We report this case due to rarity of giant abdominoscrotal arteriovenous malformations and present preoperative embolization, surgical resection, and functional anterolateral thigh flap reconstruction as a valuable treatment option of this life-threatening illness.
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http://dx.doi.org/10.1097/GOX.0000000000002725 | DOI Listing |
Urol Case Rep
September 2023
University Center of Pediatric Surgery of Western Switzerland, Division of Child and Adolescent Surgery, Department of Women, Child and Adolescent, Geneva University Hospitals, Department of Pediatrics, Gynecology and Obstetrics, University of Geneva, Rue Willy-Donzé 6, 1205, Geneva, Switzerland.
Abdominoscrotal hydrocele (ASH) is a rare condition characterized by a large scrotal and abdominal fluid-filled sac. An inguinal surgical approach is generally described in literature. We report the case of a 7-month-old child who underwent surgical repair of bilateral ASH through bilateral transverse scrotal incisions.
View Article and Find Full Text PDFCureus
August 2021
Urology, Faculty of Medicine of São José do Rio Preto (FAMERP), São José do Rio Preto, BRA.
Abdominoscrotal hydrocele is an uncommon condition characterized by an hourglass-shaped scrotal hydrocele with an intra-abdominal component connected by an isthmus within the inguinal canal. We report a rare case of an adult patient with giant abdominoscrotal hydrocele. Despite recent trends toward less invasive treatments, in this case, the surgical approach through an inguinal incision was the better therapeutic option with a satisfactory outcome.
View Article and Find Full Text PDFInt J Surg Case Rep
November 2020
Department of Urology, Hospital Taher Sfar, 5100, Mahdia, Tunisia.
Introduction: Sarcomas are a rare entity with heterogeneous clinical behavior. We herein present the case of a giant retroperitoneal dedifferentiated liposarcoma and aim to remind the clinical, histological, and therapeutic features of this rare tumor.
Presentation Of Case: An 80-year-old patient was complaining of significant abdominoscrotal swelling.
Plast Reconstr Surg Glob Open
March 2020
Department of Radiology, University of Tokyo, Tokyo, Japan.
Genital arteriovenous malformations are rare and present unique surgical challenges in preserving urogenital function, abdominal wall integrity, and lower limb perfusion. A 32-year-old man with a giant abdominoscrotal arteriovenous malformation presented with recurrent heavy bleeding. Due to the high risk of rebleeding and fatal hemorrhage, surgery with curative intent was proposed and the patient was counseled on the risks of ischemia to the lower limb, testes, and penis.
View Article and Find Full Text PDFUrology
March 2017
Department of Surgery, Division of Urology, The Hospital for Sick Children, Toronto, Canada.
Repair of abdominoscrotal hydrocele is surgically demanding and may be associated with complications. Herein we describe a surgical technique with laparoscopic assisted approach. A 6-month boy with right hydrocele and left absent testis was surgically treated with scrotal approach using one laparoscopic port.
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