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肾嗜酸细胞瘤与颗粒性肾细胞癌。一项临床病理及DNA流式细胞术比较研究。

Renal oncocytoma and granular renal cell carcinoma. A comparative clinicopathologic and DNA flow cytometric study.

作者信息

Hartwick R W, el-Naggar A K, Ro J Y, Srigley J R, McLemore D D, Jones E C, Grignon D J, Thomas M J, Ayala A G

机构信息

Department of Pathology, University of Texas, M.D. Anderson Cancer Center, Houston 77030.

出版信息

Am J Clin Pathol. 1992 Dec;98(6):587-93. doi: 10.1093/ajcp/98.6.587.

Abstract

Twenty-three renal oncocytomas and 18 granular renal cell carcinomas (GRCC) were comparatively studied clinicopathologically and by DNA flow cytometry to delineate their differences. Of the patients with renal oncocytomas, 15 were men and 8 were women, and their ages ranged from 42 to 81 years (mean, 64 years). The gross appearance of renal oncocytomas was characteristically homogeneous tan-brown, with variable scarring, without areas of large hemorrhage, and with no apparent necrosis. Twenty-two renal oncocytomas were confined within the kidney (Robson stage I) and one tumor extended into the renal vein (stage IIIa). Twenty-two renal oncocytomas, including the stage IIIa tumor, manifested diploid DNA content and only one neoplasm showed a feature suggestive of near-diploid DNA aneuploidy. Of the 17 patients with renal oncocytomas who had adequate follow-up, none developed metastasis or died of disease. Of the patients with GRCC, 13 were men and 5 were women, and their ages ranged from 30 to 73 years (mean, 53 years). The gross appearance of GRCC was variegated, yellow to tan, and punctuated with geographic areas of necrosis. Eleven patients with GRCC were stage I, 4 were stage II, 2 were stage IIIa, and 1 patient had metastases at initial examination (stage IV). Seven GRCCs were DNA diploid, one was DNA tetraploid, and 10 tumors were DNA aneuploid. Twelve patients were alive with no evidence of disease (12 to 36 months; median, 26 months). All patients with DNA diploid neoplasm pursued benign clinical courses. One patient was alive with metastatic disease and two patients developed metastases and died of their disease; all three patients had DNA aneuploid tumors. Two patients died of other causes and one patient was lost to follow-up. Our data indicate that renal oncocytoma is a distinct clinicopathologic disease with characteristic gross, histologic, DNA flow cytometric, and biologic features that are different from GRCC.

摘要

对23例肾嗜酸细胞瘤和18例颗粒性肾细胞癌(GRCC)进行了临床病理及DNA流式细胞术对比研究,以明确它们之间的差异。肾嗜酸细胞瘤患者中,男性15例,女性8例,年龄42至81岁(平均64岁)。肾嗜酸细胞瘤大体表现特征性地为均匀的棕褐色,有不同程度的瘢痕形成,无大片出血区,无明显坏死。22例肾嗜酸细胞瘤局限于肾内(Robson I期),1例肿瘤延伸至肾静脉(IIIa期)。22例肾嗜酸细胞瘤,包括IIIa期肿瘤,表现为二倍体DNA含量,仅1例肿瘤表现出近二倍体DNA非整倍体特征。17例接受充分随访的肾嗜酸细胞瘤患者均未发生转移或死于该病。GRCC患者中,男性13例,女性5例,年龄30至73岁(平均53岁)。GRCC大体表现多样,黄色至棕褐色,有地图状坏死区。11例GRCC患者为I期,4例为II期,2例为IIIa期,1例初诊时已有转移(IV期)。7例GRCC为DNA二倍体,1例为DNA四倍体,10例肿瘤为DNA非整倍体。12例患者存活且无疾病证据(12至36个月;中位时间26个月)。所有DNA二倍体肿瘤患者临床病程呈良性。1例患者存活但有转移性疾病,2例患者发生转移并死于该病;这3例患者均有DNA非整倍体肿瘤。2例患者死于其他原因,1例患者失访。我们的数据表明,肾嗜酸细胞瘤是一种独特的临床病理疾病,具有与GRCC不同的特征性大体、组织学、DNA流式细胞术及生物学特性。

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