Autosomal dominant polycystic kidney disease (ADPKD) with multiple complications: Management challenges.

Narra J Pub Date : 2024-04-01 Epub Date: 2024-02-27 DOI:10.52225/narra.v4i1.584
Kenneth M Djajapranata, Artaria Tjempakasari
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Abstract

Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary polycystic kidney disease characterized by renal enlargement, resulting in renal failure. In Indonesia, the exact prevalence of ADPKD is unknown due to limited reports on the disease. The aim of this study was to report a case of a patient with ADPKD with multiple complications. A 54-year-old male presented to the emergency room of Dr. Soetomo Academic General Hospital, Surabaya, Indonesia, with a chief complaint of dark-red-colored urine for one week. There was a progressive abdominal enlargement over the past five years, which had become more tense and rigid for the past one month. The patient had a history of fatigue and hypertension with routine follow-up. Physical examination on admission showed normal vital signs, and the abdominal assessment revealed a palpable hard mass approximately 4 cm in size in the right upper abdomen. Laboratory test indicated anemia, leukocytosis, lymphopenia, proteinuria, hematuria, leukocyturia, and elevated serum creatinine and urea levels. Abdominal imaging using ultrasonography, computed tomography (CT) scan, and magnetic resonance imaging (MRI) revealed bilateral kidney and liver enlargement containing multiple cysts, suggesting polycystic kidney and liver disease. There was a ruptured cyst in the middle of the left kidney pole with minimal ascites found in the CT scan. The MRI exhibited the presence of multiple cysts in both kidneys, partially filled with blood. The patient was diagnosed with ADPKD, gross hematuria, acute or chronic kidney disease (CKD), urinary tract infection (UTI), normochromic-normocytic anemia, and metabolic acidosis. Dietary control with high-calorie, high-protein, and low-salt diet; fluid balance; and other symptomatic medications were initiated. It is critical to be aware of risk factors associated with the rapid progression of ADPKD in order to be able to provide a favorable impact on the disease prevention and management.

伴有多种并发症的常染色体显性多囊肾病(ADPKD):管理挑战。
常染色体显性多囊肾(ADPKD)是最常见的遗传性多囊肾,其特点是肾脏肿大,导致肾功能衰竭。在印度尼西亚,由于有关 ADPKD 的报道有限,该病的确切发病率尚不清楚。本研究旨在报告一例伴有多种并发症的 ADPKD 患者。一名 54 岁的男性患者来到印度尼西亚泗水苏托莫博士学术综合医院急诊室就诊,主诉为深红色尿液一周。患者的腹部在过去五年中逐渐增大,在过去一个月中变得更加紧张和僵硬。患者有乏力和高血压病史,常规随访。入院体检显示生命体征正常,腹部评估显示右上腹可触及约4厘米大小的硬块。实验室检查显示贫血、白细胞增多、淋巴细胞减少、蛋白尿、血尿、白细胞尿、血清肌酐和尿素水平升高。腹部超声波成像、计算机断层扫描(CT)和磁共振成像(MRI)显示双侧肾脏和肝脏肿大,内含多个囊肿,提示多囊肾和多囊肝疾病。CT 扫描发现左肾极中部有一个破裂的囊肿,腹水极少。核磁共振成像显示双肾存在多个囊肿,部分充血。患者被诊断为 ADPKD、毛细血尿、急性或慢性肾脏病(CKD)、尿路感染(UTI)、正常色素-正常红细胞性贫血和代谢性酸中毒。患者开始接受高热量、高蛋白和低盐饮食控制、液体平衡和其他对症药物治疗。了解与 ADPKD 快速进展相关的风险因素至关重要,这样才能对疾病的预防和管理产生有利影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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