Lakssir Jihad, El Aboudi Adam, Boualaoui Imad, Ibrahimi Ahmed, El-Sayegh Hachem, Nouini Yassine
Department of Urology A, Ibn Sina Hospital, University of Rabat, Morocco.
Int J Surg Case Rep. 2025 Feb;127:110800. doi: 10.1016/j.ijscr.2024.110800. Epub 2024 Dec 28.
Multilocular cystic nephroma is an uncommon condition with only few cases described in the literature, although its benign nature is well-recognized.
We present a case of a 28-year-old male patient who presented with a right flank pain, imaging suspected a multicystic renal cell carcinoma. A radical nephrectomy was performed view the size of the cyst and the high tumor complexity, which histology confirmed the diagnosis of multilocular cystic nephroma.
Multilocular cystic nephroma is a rare renal tumor with few reported cases, making preoperative differentiation from cystic renal cell carcinoma difficult and leading to nephrectomy as the preferred treatment.
Multilocular cystic nephroma is typically benign, the scarcity of diagnostic and therapeutic experience necessitates vigilant postoperative surveillance to ensure patient safety and optimal outcomes.
多房性囊性肾瘤是一种罕见病症,尽管其良性性质已得到充分认识,但文献中描述的病例较少。
我们报告一例28岁男性患者,其因右侧腰痛就诊,影像学检查怀疑为多囊性肾细胞癌。鉴于囊肿大小及肿瘤复杂性高,遂行根治性肾切除术,组织学检查确诊为多房性囊性肾瘤。
多房性囊性肾瘤是一种罕见的肾肿瘤,报道病例较少,术前难以与囊性肾细胞癌鉴别,导致肾切除术成为首选治疗方法。
多房性囊性肾瘤通常为良性,由于诊断和治疗经验匮乏,术后需进行密切监测以确保患者安全并获得最佳治疗效果。