Almutairi Fawaz, Xu Bo
Department of Pathology, King Abdulaziz University, Jeddah, Saudi Arabia; Department of Pathology and Laboratory Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
Department of Pathology and Laboratory Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
Pathol Res Pract. 2024 Feb;254:155127. doi: 10.1016/j.prp.2024.155127. Epub 2024 Jan 12.
Low grade oncocytic tumor (LOT) is a recently recognized renal oncocytic neoplasm with unique morphologic and immunohistochemical pattern (CK7 +, CD117 -) that differentiates them from oncocytoma and chromophobe renal cell carcinoma (ChrRCC).
To further evaluate the histomorphological characteristics as well as the clinical outcome of low grade oncocytic tumors, retrospectively.
Thirteen cases of LOT were identified from 463 cases of renal oncocytic neoplasm in our pathology archive. All tumors were immunostained with CK7, CD117 and other relevant markers. The pathohistological features and follow up data of these cases were recorded.
Median age of patients was 76 years old (range from 36 to 86), with male to female ratio of 2:11. None of the patients had a syndromic association/hereditary condition. Eleven tumors were unifocal in each affected kidney, and two were multifocal with 2 and 3 separated tumors, respectively. On microscopic examination, tumors show variety of growth patterns, namely solid, compact nested, focal tubular/tubuloreticular and trabecular patterns. The stroma can be hypocellular and edematous where the tumor cells are loosely arranged exhibiting cords and scattered single cell arrangement. Immunohistochemically, all thirteen cases displayed strong and diffuse CK7 positivity in tumor cells. Eleven cases were CD117 negative and the other two showed focal and weak CD117 positivity (< 5% of tumor cells). Uniform tumor cell positivity was found for AE1/3, EMA, PAX8, and e-cadherin. Negative staining results include CAIX, AMACR, CD10 and vimentin. All cases in our cohort demonstrate indolent behavior and show no evidence of disease recurrence, progression, or metastases during the follow-up period up to 96 months.
LOT is an emerging new entity of renal oncocytic neoplasm and demonstrates indolent clinical behavior. Its unique morphologic features and immunohistochemical patterns (CK7 +, CD117 -) set them apart from oncocytoma and ChrRCC.
低级别嗜酸性细胞瘤(LOT)是一种最近才被认识的肾嗜酸性肿瘤,具有独特的形态学和免疫组化模式(CK7阳性,CD117阴性),这使其与嗜酸性细胞瘤和嫌色性肾细胞癌(ChrRCC)相区别。
回顾性地进一步评估低级别嗜酸性细胞瘤的组织形态学特征以及临床结局。
从我们病理档案中的463例肾嗜酸性肿瘤中识别出13例LOT。所有肿瘤均用CK7、CD117和其他相关标志物进行免疫染色。记录这些病例的病理组织学特征和随访数据。
患者的中位年龄为76岁(范围为36至86岁),男女比例为2:11。所有患者均无综合征相关性/遗传性疾病。11个肿瘤在每个患肾中为单灶性,2个为多灶性,分别有2个和3个分离的肿瘤。显微镜检查显示,肿瘤呈现多种生长模式,即实性、紧密巢状、局灶性管状/小管状网状和小梁状模式。基质细胞稀少且水肿,肿瘤细胞排列松散,呈条索状和散在的单细胞排列。免疫组化方面,所有13例肿瘤细胞均显示强烈弥漫性CK7阳性。11例CD117阴性,另外2例显示局灶性且弱阳性的CD117阳性(<5%的肿瘤细胞)。AE1/3、EMA、PAX8和E-钙黏蛋白在肿瘤细胞中呈一致阳性。阴性染色结果包括CAIX、AMACR、CD10和波形蛋白。我们队列中的所有病例均表现为惰性病程,在长达96个月的随访期内未发现疾病复发、进展或转移的证据。
LOT是肾嗜酸性肿瘤中一种新出现的实体,具有惰性的临床行为。其独特的形态学特征和免疫组化模式(CK7阳性,CD117阴性)使其与嗜酸性细胞瘤和ChrRCC区分开来。