Department of Urology, Bagcilar Training and Research Hospital, Istanbul, Turkey.
Bagcilar Training and Research Hospital, Department of Radyology, Istanbul, Turkey.
Urologia. 2022 Aug;89(3):481-483. doi: 10.1177/03915603211001252. Epub 2021 Mar 17.
Bilateral perirenal subcapsular effusion is a rare clinical condition and is associated with several underlying etiologies. We present a 33 years old male patient with idiopathic bilateral massive subcapsular effusion.
A 33-year-old male patient presented to our outpatient clinic with bilateral flank pain and fever for 2 weeks. Bilateral perirenal subcapsular effusion was detected in intravenous contrast-enhanced CT and dynamic MRI.
Bilateral ultrasound-guided percutaneous drainage was performed by an expert uroradiologist to reduce the parenchymal pressure, Control CT imaging after 6 weeks demonstrate that bilateral normal kidneys.
It has been reported that subcapsular and perirenal effusion is a rare clinical condition that may develop secondary to causes such as Nephrotic syndrome, Eisenmenger Syndrome, Lymphangiomatosis, and Page Kidney Disease. In our case, the clinical symptoms of the patient regressed after the whole effusion fluid was drained. No underlying pathology was found in further examinations. Therefore, we present the first case of Idiopathic Bilateral Massive Perirenal Subcapsular Effusion in the literature.
双侧肾周包膜下积液是一种罕见的临床病症,与多种潜在病因有关。我们报告了一例 33 岁男性特发性双侧巨大肾周包膜下积液患者。
一名 33 岁男性患者因双侧腰痛和发热 2 周就诊于我院门诊。静脉对比增强 CT 和动态 MRI 检测到双侧肾周包膜下积液。
由一位经验丰富的泌尿放射科医生进行双侧超声引导下经皮引流,以降低实质压力。6 周后的 CT 影像检查显示双侧肾脏正常。
据报道,肾周包膜下和肾周积液是一种罕见的临床病症,可能继发于肾病综合征、Eisenmenger 综合征、淋巴管瘤病和 Page 肾病等病因。在本例中,患者的临床症状在整个积液排出后消退。进一步检查未发现潜在的病理。因此,我们在文献中首次报道了一例特发性双侧巨大肾周包膜下积液。