Bjerggaard Maiken M H, Barstad Bente
Sygehusene i Ringkjøbing Amt, Urinvejskirurgisk Afdeling, og Patologisk Institut, Ringkøbing Amt.
Ugeskr Laeger. 2005 Nov 14;167(46):4379-80.
We present two case reports of multilocular cystic nephroma (MCN). MCN is a rare benign tumor of the kidney that is difficult to differentiate from malignant tumor by diagnostic imaging (ultrasound, CT) and cytology on fine-needle aspiration. This is why most cases end up with nephrectomy and diagnosis is based on the histopathological findings. In one of our two cases, a nephrectomy was performed, and in the other the tumor was resected from the kidney. The origin of MCN is uncertain, and only about 200 cases have been reported in the literature.
我们报告两例多房性囊性肾瘤(MCN)的病例。MCN是一种罕见的肾脏良性肿瘤,通过诊断性影像学检查(超声、CT)和细针穿刺细胞学检查很难与恶性肿瘤区分开来。这就是为什么大多数病例最终都进行了肾切除术,诊断是基于组织病理学检查结果。在我们的两例病例中,一例进行了肾切除术,另一例则从肾脏切除了肿瘤。MCN的起源尚不确定,文献中仅报道了约200例病例。