Endovascular Management of Renal Artery Pseudoaneurysm in Autosomal Dominant Polycystic Kidney Disease: A Case Report.

IF 0.8 Q4 PERIPHERAL VASCULAR DISEASE Vascular Specialist International Pub Date : 2024-10-15 DOI:10.5758/vsi.240031
Garima Sharma, Hira Lal, Narayan Prasad
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Abstract

Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common hereditary kidney diseases. In addition to renal involvement, vascular complications including intracranial arterial, aortic aneurysms and dissections are common in these patients. We report the case of a 35-year-old male patient with ADPKD who presented with hematuria and was diagnosed with two intrarenal arterial pseudoaneurysms. Endovascular embolization using coils was performed to resolve these symptoms. Vascular complications are often encountered in patients with ADPKD; hence, sufficient clinical suspicion and timely diagnosis can help manage the disease. The most common causes of hematuria in ADPKD patients are cyst hemorrhage or infection; however, vascular aneurysms should also be considered a possibility.

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常染色体显性多囊肾病肾动脉假性动脉瘤的血管内治疗:病例报告。
常染色体显性多囊肾(ADPKD)是最常见的遗传性肾病之一。除肾脏受累外,血管并发症(包括颅内动脉、主动脉瘤和动脉夹层)在这些患者中也很常见。我们报告了一例 35 岁男性 ADPKD 患者的病例,他出现血尿并被诊断出患有两个肾内动脉假性动脉瘤。使用线圈进行血管内栓塞治疗后,这些症状得以缓解。ADPKD 患者经常会出现血管并发症,因此,充分的临床怀疑和及时诊断有助于控制病情。ADPKD 患者血尿最常见的原因是囊肿出血或感染,但也应考虑血管动脉瘤的可能性。
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来源期刊
CiteScore
1.10
自引率
11.10%
发文量
29
审稿时长
17 weeks
期刊最新文献
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