AUTOTRANSPLANTATION WITH EXTRACORPORAL RECONSTRUCTION OF RENAL VESSELS: A CLINICAL CASE OF “THE NUTCRACKER SYNDROME” AND LEFT RENAL ARTERIES HYPOPLASIA COMBINATION

I. Kobza, I. R. Nestetenko, R. Zhuk, Y. Mota
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Abstract

Ex vivo kidney autotransplantation with renal artery reconstruction is an effective method of surgical correction of vascular abnormalities (fibromuscular dysplasia, hypoplasia, and renal artery aneurysms) showing good long-term results. The combination of renal artery abnormalities with aorto-mesenteric compression syndrome (“the nutcracker” syndrome) is extremely rare and complicates the diagnosis making greatly. Renal artery hypoplasia is an abnormality that is rarely diagnosed and may not manifest clinically in the absence of contralateral kidney pathology as well as its vascular structures. Renal hypoplasia may be caused by mutations in the kidney development genes (HNF1B, PAX2, PBX1) and/or several environmental factors such as intrauterine growth retardation, maternal diseases (diabetes, hypertension), medication taken by the mother (renin-angiotensin system inhibitors or nonsteroidal anti-inflammatory drugs) and intoxication (smoking and alcohol). Premature delivery (before the 36th week) is also a risk factor due to incomplete nephrogenesis. Renal arteries hypoplasia is associated with fibromuscular dysplasia in most cases. The disease is characterized by non-inflammatory non-uniform focal hyperplasia of the renal artery wall with damage to small and medium arteries. Simultaneous damage to two or more vascular segments is detected in 25% of patients. A clinical case of successful treatment of “the nutcracker” syndrome (annular renal vein) combined with hypoplasia of the left main and accessory renal arteries associated with fibromuscular dysplasia is described. A 27-year-old female was admitted to the Department of Vascular Surgery of Municipal Noncommercial Enterprise of the Lviv Regional Council “Lviv Regional Clinical Hospital” on October 4, 2021, with complaints of pain in the left lumbar region and the left half of the abdomen, hematuria, proteinuria, a persistent increase in blood pressure. Ultrasound of the renal veins: the left renal vein in the aorto-mesenteric segment was not visualized, the posterior portion of the left renal vein was determined. Peak systolic velocity was up to 230 cm/s at the point of confluence with the inferior vena cava and 28 cm/s more distally. The vein was up to 12.0 mm in the renal hilum and up to 11.0 mm in the middle third. MSCT of the abdominal cavity, retroperitoneal space and pelvic organs: CT signs of pyelonephritis of the left kidney. Hypoplasia of the left kidney. Reactive para-aortic lymphadenopathy on the left. Hypoplastic left renal artery (3,8 mm) and presense of accessory ones, annular left renal vein. Angiomyolipoma of the right kidney (2,6 cm). Varicose veins of the small pelvis on the left. The patient underwent surgical treatment, namely ex vivo autovenous prosthetic repair of the left renal artery with autotransplantation of the left kidney. The course of the postoperative period was without complications, the reconstruction was functioning. Ultrasound of the renal vessels (1 week after the surgery): the blood flow was located in the renal hilum in the course of Doppler sonography of intrarenal branches. Venous outflow was unobstructed. Corticomedullary differentiation was marked satisfactorily. The study presented by us demonstrates the effectiveness of kidney autotransplantation for the correction of renal vascular abnormalities. Though of a solitary nature, the combination of renal vessels abnormalities complicates significantly the course of the disease and the possibilities of this pathology diagnostics.
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肾血管颞外重建自体移植术:胡桃钳综合征 "和左肾动脉发育不良合并症的临床病例
肾动脉重建的体外肾脏自体移植是手术矫正血管异常(纤维肌发育不良、发育不良和肾动脉瘤)的有效方法,长期效果良好。肾动脉畸形与主动脉-肠系膜压迫综合征("胡桃钳 "综合征)并发的情况极为罕见,使诊断变得非常复杂。肾动脉发育不全是一种很少被诊断出来的异常,在没有对侧肾脏病变及其血管结构的情况下,临床表现可能并不明显。肾动脉发育不全可能由肾脏发育基因(HNF1B、PAX2、PBX1)突变和/或一些环境因素引起,如宫内发育迟缓、母体疾病(糖尿病、高血压)、母亲服用的药物(肾素-血管紧张素系统抑制剂或非类固醇抗炎药)和中毒(吸烟和饮酒)。早产(第 36 周之前)也是一个风险因素,因为肾脏生成不完全。肾动脉发育不良在大多数情况下与纤维肌发育不良有关。该病的特点是肾动脉壁出现非炎症性非均匀性局灶性增生,中小动脉受损。25%的患者会发现两个或多个血管节段同时受损。本文描述了一个成功治疗 "胡桃钳 "综合征(环状肾静脉)合并左肾主动脉和附属动脉发育不良并伴有纤维肌肉发育不良的临床病例。2021 年 10 月 4 日,一名 27 岁女性因左腰部和左半部腹部疼痛、血尿、蛋白尿、血压持续升高等主诉入住利沃夫州委员会市立非商业企业 "利沃夫州临床医院 "血管外科。肾静脉超声检查:左肾静脉主动脉-肠系膜段未显影,左肾静脉后段确定。与下腔静脉汇合处的收缩峰值速度高达 230 厘米/秒,更远处为 28 厘米/秒。该静脉在肾门处长达 12.0 毫米,在中间三分之一处长达 11.0 毫米。腹腔、腹膜后间隙和盆腔器官的 MSCT:左肾肾盂肾炎的 CT 征象。左肾发育不良。左侧主动脉旁反应性淋巴结病。左肾动脉发育不良(3.8 毫米),存在附属动脉,左肾静脉呈环状。右肾血管瘤(2.6 厘米)。左侧小骨盆静脉曲张。患者接受了手术治疗,即左肾动脉体外自体静脉假体修复术和左肾自体移植术。术后无并发症,重建功能正常。肾血管超声波检查(术后一周):在对肾内分支进行多普勒超声波检查时,血流位于肾门。静脉流出通畅。皮质髓质分化标志令人满意。我们进行的这项研究证明了肾脏自体移植手术在矫正肾脏血管异常方面的有效性。虽然肾血管异常是一种单发性疾病,但合并肾血管异常会使病程和病理诊断的可能性大大复杂化。
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CURRENT STATUS AND PERSPECTIVES OF THE USE OF SPECIES OF THE GENUS MELAMPYRUM IN MEDICINE AND PHARMACY AUTOTRANSPLANTATION WITH EXTRACORPORAL RECONSTRUCTION OF RENAL VESSELS: A CLINICAL CASE OF “THE NUTCRACKER SYNDROME” AND LEFT RENAL ARTERIES HYPOPLASIA COMBINATION MORPHOFUNCTIONAL STATE OF PANCREAS IN RATS WITH DIABETES MELLITUS FEATURES OF THE PHYSIOLOGY OF THE POSTPARTUM PERIOD AFTER CAESAREAN SECTION CLINICAL CASE OF KERATOACANTHOMA
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