Lopez-Beltran Antonio, Paner Gladell, Blanca Ana, Montironi Rodolfo, Tsuzuki Toyonori, Nagashima Yoji, Chuang Shi-Sung, Win Khin Than, Madruga Leo, Raspollini Maria R, Cheng Liang
Department of Pathology and Surgery, Unit of Anatomical Pathology, Faculty of Medicine, University of Cordoba, 14004, Cordoba, Spain.
Section of Urology, Departments of Pathology and Surgery, University of Chicago, Chicago, IL, USA.
Virchows Arch. 2017 Jun;470(6):703-709. doi: 10.1007/s00428-017-2117-z. Epub 2017 Apr 28.
In this report, we summarized the clinicopathologic features of ten cases of lymphoepithelioma-like carcinoma (LELC) of the upper urinary tract (ureter n = 6; renal pelvis n = 4), a rare variant of urothelial cancer characterized by a malignant epithelial component densely infiltrated by lymphoid cells. The initial diagnosis was made on radical nephrectomy in five cases, nephroureterectomy in three cases, and ureterectomy in two others. Four patients had pathologic stage T1 (n = 2) or T2 (n = 2) tumors, and six patients had stage pT3 disease. Microscopically, all tumors contained pure (n = 3) or predominant (n = 7) LELC, which composed 60 to 80% of the entire tumor. Non-LELC tumor component was adenocarcinoma (n = 2), spindle cell carcinoma (n = 1), or high-grade conventional urothelial carcinoma (n = 4). The LELC component was characterized by indistinct cytoplasmic borders and a syncytial growth pattern. Immunohistochemical staining showed LELC to be positive for cytokeratin AE1/AE3, CK7, CK34ßE12 (rare cells), CK5/6 (rare cells), and CK20 (rare cells); rare cells were p40 positive. GATA 3 was positive in all cases in a variable proportion of cells (20-80%). Lymphoid markers showed a polyclonal proliferation of predominant T cells admixed with B cells. In situ hybridization for the HPV genome was negative in all ten cases. Survival analysis showed no differences between LELC and conventional upper urinary tract urothelial carcinoma, pT classification being the only significant prognostic parameter. Morphologic recognition and distinction from other (non-)neoplastic lesions with prominent lymphoid stroma are critical for its clinical management.
在本报告中,我们总结了10例上尿路淋巴上皮瘤样癌(LELC)(输尿管6例;肾盂4例)的临床病理特征,这是一种罕见的尿路上皮癌变体,其特征为恶性上皮成分被淋巴细胞密集浸润。5例患者经根治性肾切除术确诊,3例经肾输尿管切除术确诊,另2例经输尿管切除术确诊。4例患者的肿瘤病理分期为T1(2例)或T2(2例),6例患者为pT3期疾病。镜下,所有肿瘤均含有纯(3例)或主要(7例)LELC成分,占整个肿瘤的60%至80%。非LELC肿瘤成分包括腺癌(2例)、梭形细胞癌(1例)或高级别传统尿路上皮癌(4例)。LELC成分的特点是胞质边界不清,呈合体生长模式。免疫组化染色显示LELC对细胞角蛋白AE1/AE3、CK7、CK34βE12(罕见细胞)、CK5/6(罕见细胞)和CK20(罕见细胞)呈阳性;罕见细胞p40阳性。GATA 3在所有病例中均呈阳性,阳性细胞比例各不相同(20% - 80%)。淋巴标志物显示主要为T细胞与B细胞混合的多克隆增殖。10例病例的HPV基因组原位杂交均为阴性。生存分析显示LELC与传统上尿路尿路上皮癌之间无差异,pT分类是唯一重要的预后参数。形态学识别以及与其他具有显著淋巴间质的(非)肿瘤性病变相鉴别对其临床管理至关重要。