Artinyan Elizabeth, Valcheva Evelina, Vaysilova Marina, Dimov Nikolay
Nephrology Clinic, University Hospital "Sv. Georgi" Plovdiv, 4000 Plovdiv, Bulgaria.
Second Department of Internal Diseases, Section of Nephrology, Medical University Plovdiv Bulgaria, 4000 Plovdiv, Bulgaria.
Reports (MDPI). 2025 Jul 25;8(3):121. doi: 10.3390/reports8030121.
Spontaneous renal hematoma, also known as Wunderlich syndrome (WS), is a rare disease characterized by the acute onset of spontaneous renal hemorrhage into the subcapsular, perirenal, and/or pararenal spaces without a history of prior trauma. WS can be a life-threatening condition due to hemorrhagic shock; consequently, prompt diagnosis and a therapeutic approach are essential for favorable outcomes. Treatment ranges from conservative management to surgical intervention. The most common etiologies are neoplasms and vascular diseases, but WS can also be observed in patients undergoing hemodialysis. In patients with end-stage renal disease (ESRD), especially those on hemodialysis, acquired cystic kidney disease and renal cell carcinoma are among the primary causes of WS. Although less common, WS can develop in dialysis patients even in the absence of traditional (primary) risk factors. In general, patients with chronic kidney disease (CKD) have a paradoxical hemostatic profile, likely explaining their higher tendency to bleed, so WS can occur without existing predisposing factors. The multifactorial pathogenesis in these patients includes functional platelet abnormalities, intimal arterial fibrosis, chronic inflammation, and oxidative stress associated with ESRD. The use of hemodialysis-related antithrombotic medications could serve as another contributing factor increasing the risk of bleeding. We present a case report of a 62-year-old male on chronic dialysis who developed sudden right-sided lumbar pain and hematuria during dialysis without evidence of prior trauma. Imaging revealed a large subcapsular hematoma of the right kidney. Further investigations did not reveal additional risk factors in this instance; however, his routinely used hemodialysis-related antithrombotic medications were potentially a contributing factor. Despite conservative treatment, his condition worsened, and the hematoma enlarged, requiring emergency nephrectomy. Postoperatively, his condition gradually improved. This case highlights the importance of considering WS in hemodialysis patients, even without the presence of traditional risk factors, as well as including WS in the differential diagnosis of acute abdominal pain.
自发性肾血肿,也称为温德利希综合征(WS),是一种罕见疾病,其特征为在无既往创伤史的情况下,急性发生自发性肾出血进入肾包膜下、肾周和/或肾旁间隙。由于出血性休克,WS可能是一种危及生命的病症;因此,及时诊断和治疗方法对于取得良好预后至关重要。治疗范围从保守治疗到手术干预。最常见的病因是肿瘤和血管疾病,但在接受血液透析的患者中也可观察到WS。在终末期肾病(ESRD)患者中,尤其是那些接受血液透析的患者,获得性囊性肾病和肾细胞癌是WS的主要原因之一。尽管不太常见,但即使没有传统(主要)危险因素,透析患者也可能发生WS。一般来说,慢性肾病(CKD)患者具有矛盾的止血特征,这可能解释了他们更高的出血倾向,因此WS可能在没有现有易感因素的情况下发生。这些患者的多因素发病机制包括功能性血小板异常、内膜动脉纤维化、慢性炎症以及与ESRD相关的氧化应激。使用与血液透析相关的抗血栓药物可能会增加出血风险。我们报告一例62岁男性慢性透析患者,在透析期间突然出现右侧腰痛和血尿,无既往创伤证据。影像学检查显示右肾有一个大的包膜下血肿。在此病例中,进一步检查未发现其他危险因素;然而,他常规使用的与血液透析相关的抗血栓药物可能是一个促成因素。尽管进行了保守治疗,他的病情仍恶化,血肿增大,需要紧急肾切除术。术后,他的病情逐渐好转。该病例强调了在血液透析患者中考虑WS的重要性,即使没有传统危险因素,以及将WS纳入急性腹痛的鉴别诊断中。