Mendez Teresita, Bahmad Hisham F, Polit Francesca, Carpio Nicole, Gill Arman, Burke William F, Bhandari Akshay, Poppiti Robert, Omarzai Yumna
Florida International University, Herbert Wertheim College of Medicine, Miami, FL, USA.
Mount Sinai Medical Center, Arkadi M. Rywlin M.D. Department of Pathology and Laboratory Medicine, Miami Beach, FL, USA.
Autops Case Rep. 2024 Jun 21;14:e2024498. doi: 10.4322/acr.2024.498. eCollection 2024.
Localized cystic kidney disease (LCKD) is a distinct renal disorder characterized by the presence of cysts within specific regions of the kidneys. We present a rare case of a 41-year-old African American man, who presented to our medical center with lower urinary tract symptoms and gross hematuria. The initial assessment culminated in the identification of an uncomplicated urinary tract infection, prompting the prescription of appropriate oral antibiotic therapy. On follow-up after 5 months, the patient presented with gross hematuria. Imaging studies revealed a mixed-density cystic lesion of 2.6 cm situated within the interpolar region of the right kidney. This cystic lesion exhibited intricate septations at the superior pole of the kidney. Robotic-assisted right partial nephrectomy was performed, and pathologic examination was diagnostic for LCKD. This report not only underscores the uniqueness of LCKD but also presents a comprehensive review of the existing literature that pertains to this condition. Particular emphasis is placed upon its inherent benign behavior and its marked divergence from the progressive trajectory commonly associated with other renal diseases. We also explored the incidental findings of the disease, its diverse clinical symptomatology, conceivable etiological underpinnings, and the array of diagnostic modalities used. Finally, similarities in histopathologic findings with polycystic kidney disease and other entities are discussed, underscoring the importance of accurate diagnosis and management.
局限性囊性肾病(LCKD)是一种独特的肾脏疾病,其特征是在肾脏的特定区域存在囊肿。我们报告了一例罕见病例,一名41岁的非裔美国男性因下尿路症状和肉眼血尿就诊于我们的医疗中心。初步评估最终确定为单纯性尿路感染,遂给予适当的口服抗生素治疗。5个月后的随访中,患者出现肉眼血尿。影像学检查显示右肾极间区域有一个2.6厘米的混合密度囊性病变。该囊性病变在肾上级表现出复杂的分隔。实施了机器人辅助右肾部分切除术,病理检查诊断为LCKD。本报告不仅强调了LCKD的独特性,还对与该疾病相关的现有文献进行了全面综述。特别强调了其固有的良性行为以及与其他肾脏疾病通常相关的进行性病程的显著差异。我们还探讨了该疾病的偶然发现、其多样的临床症状、可能的病因基础以及所使用的一系列诊断方法。最后,讨论了其组织病理学发现与多囊肾病和其他实体的相似性,强调了准确诊断和管理的重要性。