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Endovascular Management of Ruptured Renal Angiomyolipoma: A Case Report

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Renal angiomyolipoma is classified as a benign tumour comprising fat, smooth muscle cells, and vascular tissue. Renal giant angiomyolipoma with rupture is a relatively rare clinical emergency condition. Here, the authors present a case of a 37-year-old female patient who presented with complaints of right flank pain for six hours. The patient was anaemic and did not have haematuria. On non contrast Computed Tomography (CT) imaging, there was a right perirenal haematoma with a mixed-density, fat-containing tumour in the upper interpolar region of the right kidney. On Contrast-Enhanced Computed Tomography (CECT) imaging, the right renal tumour showed multiple abnormal tortuous vessels with moderate to intense enhancement, consistent with a large angiomyolipoma. She was managed with primary therapeutic endovascular embolisation for a ruptured right renal angiomyolipoma under local anaesthesia via a right transfemoral artery approach. The procedure was uneventful, and postembolisation syndrome was managed with medications. The patient was discharged in a stable condition. During the one-month follow-up, the patient’s symptoms improved, and the need for major surgery like nephrectomy was avoided. Super selective embolisation to devascularise the tumour and preserve renal parenchyma was done under local anaesthesia via a right transfemoral approach without any complications. Postembolisation syndrome was managed medically
Title: Endovascular Management of Ruptured Renal Angiomyolipoma: A Case Report
Description:
Renal angiomyolipoma is classified as a benign tumour comprising fat, smooth muscle cells, and vascular tissue.
Renal giant angiomyolipoma with rupture is a relatively rare clinical emergency condition.
Here, the authors present a case of a 37-year-old female patient who presented with complaints of right flank pain for six hours.
The patient was anaemic and did not have haematuria.
On non contrast Computed Tomography (CT) imaging, there was a right perirenal haematoma with a mixed-density, fat-containing tumour in the upper interpolar region of the right kidney.
On Contrast-Enhanced Computed Tomography (CECT) imaging, the right renal tumour showed multiple abnormal tortuous vessels with moderate to intense enhancement, consistent with a large angiomyolipoma.
She was managed with primary therapeutic endovascular embolisation for a ruptured right renal angiomyolipoma under local anaesthesia via a right transfemoral artery approach.
The procedure was uneventful, and postembolisation syndrome was managed with medications.
The patient was discharged in a stable condition.
During the one-month follow-up, the patient’s symptoms improved, and the need for major surgery like nephrectomy was avoided.
Super selective embolisation to devascularise the tumour and preserve renal parenchyma was done under local anaesthesia via a right transfemoral approach without any complications.
Postembolisation syndrome was managed medically.

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