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肾动静脉畸形致血尿:病例报告及文献复习。

Renal arteriovenous malformation causing hematuria: Case report and review of the literature.

机构信息

Clinical Medical College, Jining Medical University, Jining, China.

Department of Urology, Affiliated Hospital of Jining Medical University, Jining, China.

出版信息

Medicine (Baltimore). 2023 Aug 25;102(34):e34547. doi: 10.1097/MD.0000000000034547.

Abstract

RATIONALE

Renal arteriovenous malformations are rare vascular morphological anomalies that can be classified as congenital, idiopathic and acquired, of which congenital renal arteriovenous malformations are the most common. This disease is a rare cause of hematuria. In this case report, we report the diagnosis and treatment of a patient with renal arteriovenous malformation. We also review the symptoms, diagnosis and treatment of renal arteriovenous malformations in the published literature.

PATIENT CONCERNS

A 35-year-old female patient presented to a local hospital with right-sided lumbar abdominal pain with hematuria for 2 days. Physical examination showed percussion pain in the right renal area. Laboratory tests such as routine blood and blood biochemistry did not show any significant abnormalities when the patient entered the hospital. Considering the patient's medical history, a urological computed tomography scan showed blood accumulation in the right renal pelvis, upper middle ureter and bladder. Subsequently, routine blood tests showed that the patient's red blood cells and hemoglobin continued to decrease. An emergency renal arteriogram was performed, which showed a tortuous right upper renal pole branch artery and multiple thickened veins communicating with it.

DIAGNOSIS

This patient was diagnosed with cirsoid renal arteriovenous malformation.

INTERVENTIONS

Renal artery embolization was performed immediately after the renal arteriogram was performed on the patient.

OUTCOMES

On review of the angiogram, the tortuous right upper renal pole branch artery was found to be obstructed, and the thickened vein disappeared, and the renal vein was normally visualized in due course. On the third postoperative day, the patient was free of hematuria. Physical examination showed no percussion pain in the renal area. The patient healed and was discharged. A 1-year follow-up was performed and the patient gave feedback that she no longer had symptoms such as back pain and hematuria in her daily life.

LESSONS

This case illustrates that early use of vascular interventions is an important method for the diagnosis and treatment of cirsoid renal arteriovenous malformations.

摘要

背景

肾动静脉畸形是一种罕见的血管形态学异常,可分为先天性、特发性和获得性,其中先天性肾动静脉畸形最为常见。这种疾病是血尿的罕见原因。在本病例报告中,我们报告了一例肾动静脉畸形患者的诊断和治疗。我们还回顾了文献中报道的肾动静脉畸形的症状、诊断和治疗。

患者关注

一名 35 岁女性患者因右侧腰腹部疼痛伴血尿 2 天就诊于当地医院。体格检查显示右肾区叩击痛。患者入院时常规血液和血液生化检查未发现明显异常。考虑到患者的病史,泌尿科计算机断层扫描显示右肾盂、中上输尿管和膀胱内有血液积聚。随后,常规血液检查显示患者的红细胞和血红蛋白持续下降。行紧急肾动脉造影显示右肾上极分支动脉迂曲,多条增厚静脉与之相通。

诊断

该患者被诊断为串珠状肾动静脉畸形。

干预措施

在对患者进行肾动脉造影后,立即进行肾动脉栓塞。

结果

血管造影复查显示迂曲的右肾上极分支动脉闭塞,增厚的静脉消失,随后正常显示肾静脉。术后第 3 天,患者血尿消失。体格检查显示肾区无叩击痛。患者痊愈出院。进行了 1 年的随访,患者反馈日常生活中不再有腰痛和血尿等症状。

教训

本病例说明早期采用血管介入是诊断和治疗串珠状肾动静脉畸形的重要方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a003/10470693/9ed42a821536/medi-102-e34547-g001.jpg

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