Lane Brian R, Aydin Hakan, Danforth Teresa L, Zhou Ming, Remer Erick M, Novick Andrew C, Campbell Steven C
Glickman Urological and Kidney Institute, Cleveland Clinic, Cleveland, Ohio 44195, USA.
J Urol. 2008 Sep;180(3):836-43. doi: 10.1016/j.juro.2008.05.041. Epub 2008 Jul 16.
Angiomyolipomas classically present radiographically as fat containing lesions but some fail to demonstrate fat content. Histologically confirmed angiomyolipomas uniformly follow a benign course but rare epithelioid variants of angiomyolipoma can recur and metastasize. We investigated the clinical, radiographic and histological characteristics of each angiomyolipoma subtype.
Pertinent data were recorded for 209 patients surgically treated for angiomyolipoma in 219 kidneys from 1981 to 2007. Classic and fat poor angiomyolipomas were classified radiographically based on the presence or absence of fat and classified histologically based on the presence of triphasic, monophasic or epithelioid histology.
Median radiographic size was 3.2, 4.9 and 10 cm in patients with a single angiomyolipoma (59% of patients), multiple angiomyolipomas and tuberous sclerosis (probable or definite), respectively. In these 3 groups 65%, 47% and 33% of lesions were not suspected radiographically (fat poor angiomyolipoma). Fat poor angiomyolipomas were more commonly single, smaller and in older patients. Triphasic histology was evident in 76% of angiomyolipomas with 16% demonstrating a predominance of 1 component and 8% containing epithelioid features. Despite potentially aggressive findings in 18% (eg presence within the perinephric fat, lymph node involvement) no angiomyolipoma recurred during a mean followup of 3.4 years (range 0 to 24). A total of 28 (13%) patients with angiomyolipoma had concomitant renal cell carcinoma.
A surprisingly high number of resected angiomyolipomas was not suspected radiographically indicating the importance of precise radiographic characterization to minimize nephrectomy for fat poor angiomyolipoma, which should remain a research priority. In this sizeable single institution series no triphasic, monophasic or epithelioid angiomyolipoma recurred despite potentially aggressive findings in a substantial proportion of cases.
血管平滑肌脂肪瘤在影像学上典型表现为含脂肪的病变,但有些病变未显示脂肪成分。组织学确诊的血管平滑肌脂肪瘤通常病程良性,但罕见的上皮样血管平滑肌脂肪瘤变异型可复发和转移。我们研究了每种血管平滑肌脂肪瘤亚型的临床、影像学和组织学特征。
记录了1981年至2007年期间209例接受手术治疗的血管平滑肌脂肪瘤患者(共219个肾脏)的相关数据。经典型和脂肪含量少的血管平滑肌脂肪瘤根据影像学上有无脂肪进行分类,并根据是否存在三相、单相或上皮样组织学进行组织学分类。
单发血管平滑肌脂肪瘤患者(占患者总数的59%)、多发血管平滑肌脂肪瘤患者以及结节性硬化症(可能或确诊)患者的影像学中位大小分别为3.2 cm、4.9 cm和10 cm。在这三组中,分别有65%、47%和33%的病变在影像学上未被怀疑(脂肪含量少的血管平滑肌脂肪瘤)。脂肪含量少的血管平滑肌脂肪瘤更常见为单发、体积较小且患者年龄较大。76%的血管平滑肌脂肪瘤表现为三相组织学,16%表现为一种成分占优势,8%含有上皮样特征。尽管18%的病例有潜在的侵袭性表现(如肾周脂肪内存在、淋巴结受累),但在平均3.4年(范围0至24年)的随访期间,没有血管平滑肌脂肪瘤复发。共有28例(13%)血管平滑肌脂肪瘤患者合并肾细胞癌。
在影像学上未被怀疑的切除血管平滑肌脂肪瘤数量惊人地多,这表明精确的影像学特征对于尽量减少因脂肪含量少的血管平滑肌脂肪瘤而进行肾切除术的重要性,这仍是一个研究重点。在这个规模较大的单机构系列研究中,尽管相当一部分病例有潜在的侵袭性表现,但三相、单相或上皮样血管平滑肌脂肪瘤均未复发。