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1. Endovascular treatment of intrarenal aneurysms bleeding and angiomyolipomas in a patient with tuberous sclerosis and polycystic kidney disease.

Author

Leite T, Pazinato LV, Vidal MJA, Freitas D, and Leal Filho JMM

Subjects
Humans, Hematuria complications, Hemorrhage etiology, Hemorrhage therapy, Angiomyolipoma complications, Angiomyolipoma therapy, Polycystic Kidney, Autosomal Dominant complications, Tuberous Sclerosis genetics, Polycystic Kidney Diseases complications, Polycystic Kidney Diseases therapy, Kidney Neoplasms complications
Abstract

Tuberous sclerosis complex (TSC) and autosomal dominant polycystic kidney disease (ADPKD) are conditions related to renal failure that can rarely occur in association as a contiguous gene syndrome. Angiomyolipomas (AMLs) are renal tumors strongly related to TSC that may rupture and cause life-threatening bleedings. We present a patient with TSC, ADPKD, and renal AMLs with persistent hematuria requiring blood transfusion. The persistent hematuria was successfully treated through endovascular embolization, a minimally invasive nephron sparing technique.

Published
2023
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