Smith Nathaniel E, Epstein Jonathan I, Parwani Anil V, Netto George J, Illei Peter B, Powell Kerry, Allaf Mohamed E, Argani Pedram
Department of Pathology, The Johns Hopkins Medical Institutions, Baltimore, MD, 21042, USA.
Department of Pathology, The Johns Hopkins Medical Institutions, Baltimore, MD, 21042, USA; Department of Urology, The Johns Hopkins Medical Institutions, Baltimore, MD, 21042, USA; Department of Oncology, The Johns Hopkins Medical Institutions, Baltimore, MD, 21042, USA.
Hum Pathol. 2015 Jun;46(6):894-905. doi: 10.1016/j.humpath.2015.02.003. Epub 2015 Feb 19.
We describe 6 cases of a biphasic renal neoplasm, which we designate smooth muscle and adenoma-like renal tumor, which do not cleanly fit any category as currently defined. There were 4 females and 2 males (age, 27-70 years); neither male had a history of hormone exposure. All 5 neoplasms with available history were discovered incidentally on imaging studies with sizes ranging from 4 to 20 cm. The stroma was composed of smooth muscle fascicles alternating with looser, edematous areas; none of the cases contained ovarian-like stroma. The complex but cytologically benign epithelial component consisted of tubulopapillary nodules, branching tubules, clefts, and large cysts. The stroma of all of the cases labeled diffusely for desmin. Estrogen receptor labeling was absent in 4 cases with only minimal (<10%) weak labeling in the remaining 2. The epithelial component of each case labeled diffusely for cytokeratin 7 and was patchy for α-methyl-CoA racemase (P504S). Carbonic anhydrase IX, HMB45, WT-1, and inhibin were negative. None of the 5 cases tested demonstrated trisomies of chromosome 7 or 17 by fluorescence in situ hybridization. Two patients with significant follow-up are disease free at 18.5 and 2.5 years. Smooth muscle and adenoma-like renal tumor could potentially represent a variant of mixed epithelial stromal tumor, which would expand its reported spectrum. However, the absence of clinical history of hormone exposure, predominance of smooth muscle with lack of ovarian-like stroma, prominence of epithelial nodules, and typical absence of estrogen receptor labeling suggest that it may represent a distinct entity.
我们描述了6例双相性肾肿瘤,我们将其命名为平滑肌和腺瘤样肾肿瘤,它们不完全符合目前定义的任何类别。有4名女性和2名男性(年龄27 - 70岁);两名男性均无激素暴露史。所有5例有可用病史的肿瘤均在影像学检查中偶然发现,大小范围为4至20厘米。间质由平滑肌束与较疏松的水肿区域交替组成;所有病例均无卵巢样间质。复杂但细胞学上良性的上皮成分由管状乳头结节、分支小管、裂隙和大囊肿组成。所有病例的间质弥漫性标记结蛋白。4例雌激素受体标记阴性,其余2例仅有极少(<10%)的弱阳性标记。每个病例的上皮成分弥漫性标记细胞角蛋白7,α - 甲基辅酶A消旋酶(P504S)呈斑片状标记。碳酸酐酶IX、HMB45、WT - 1和抑制素均为阴性。通过荧光原位杂交,5例检测病例均未显示7号或17号染色体三体。两名有显著随访结果的患者在18.5年和2.5年时无疾病。平滑肌和腺瘤样肾肿瘤可能代表混合性上皮间质肿瘤的一种变异型,这将扩大其报道的谱系。然而,缺乏激素暴露的临床病史、以平滑肌为主且无卵巢样间质、上皮结节突出以及典型的雌激素受体标记阴性表明它可能代表一种独特的实体。