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伴有平滑肌瘤样间质的肾细胞癌——这种罕见实体的进一步免疫组化及分子遗传学特征

Renal cell carcinoma with leiomyomatous stroma--further immunohistochemical and molecular genetic characteristics of unusual entity.

作者信息

Peckova Kvetoslava, Grossmann Petr, Bulimbasic Stela, Sperga Maris, Perez Montiel Delia, Daum Ondrej, Rotterova Pavla, Kokoskova Bohuslava, Vesela Pavla, Pivovarcikova Kristyna, Bauleth Kevin, Branzovsky Jindrich, Dubova Magdalena, Hora Milan, Michal Michal, Hes Ondrej

机构信息

Department of Pathology, Charles University, Medical Faculty and Charles University Hospital, Plzen, Czech Republic.

Department of Pathology, University Hospital Dubrava, Zagreb, Croatia.

出版信息

Ann Diagn Pathol. 2014 Oct;18(5):291-6. doi: 10.1016/j.anndiagpath.2014.08.004. Epub 2014 Aug 15.

Abstract

UNLABELLED

Renal cell carcinoma (RCC) with leiomyomatous stroma (RCCLS) is a recently recognized entity with indolent biological behavior. The diagnostic implication of absence/presence of VHL gene mutation, VHL hypermethylation, or/and loss of heterozygosity of chromosome 3p (LOH 3p) is widely discussed. Criteria for establishing a diagnosis of RCCLS are still lacking. Fifteen RCCLSs were retrieved from our registry. The cases were studied with consideration to the morphology, immunohistochemistry, and molecular genetics. All cases were composed of low-grade epithelial cells with clear cytoplasm arranged in nests intermingled with abundant leiomyomatous stroma. Age range of the patients was 33 to 78 years. The tumor size ranged from 1.5 to 11 cm. Six of the patients were males, and 9, females. Of the 15 tumors sent for molecular genetic testing, only 12 cases were analyzable. All cases were analyzable immunohistochemically. Of 12 of these cases, 5 showed complete absence of VHL gene mutation, VHL hypermethylation, and LOH 3p. Of these 5 cases, 3 were positive for cytokeratin 7 (CK 7). All of the 5 cases were positive for carbonic anhydrase 9, vimentin, and CD10. The remaining 7 of 12 genetically analyzable cases were found to have had VHL hypermethylation, LOH 3p, VHL gene mutation, or a combination of the former 2 characteristics. These 7 cases were positive for vimentin. Variable reactivity was found for CK 7, carbonic anhydrase 9, α-methylacyl-CoA racemase, and CD10. In 1 of these 7 cases, gains on chromosomes 7 and 17 as well as hypermethylation of VHL gene were found. This case was considered as clear cell RCC with aberrant status of chromosomes 7 and 17.

CONCLUSIONS

(1) Leiomyomatous stroma is not specific for the so called RCCLS. It can be seen also in otherwise typical clear cell RCCs. (2) There are no characteristic morphological/immunohistochemical features unique for "RCCLS." (3) Our results indicate that only tumors with the absence of the VHL gene mutation, hypermethylation, and LOH 3p can be diagnosed as RCCLS. (4) Relation of RCCs with a prominent smooth muscle stroma to the renal angiomyoadenomatous tumor/clear cell papillary (tubopapillary) RCC is not clearly evident from our study and has to be further analyzed on larger cohort of the patients.

摘要

未标注

伴有平滑肌瘤样间质的肾细胞癌(RCCLS)是一种最近才被认识的具有惰性生物学行为的实体。VHL基因突变、VHL高甲基化或/和3号染色体杂合性缺失(3p LOH)的有无所具有的诊断意义已得到广泛讨论。目前仍缺乏建立RCCLS诊断的标准。从我们的病例登记中检索出15例RCCLS。对这些病例进行了形态学、免疫组织化学和分子遗传学研究。所有病例均由低级别上皮细胞组成,细胞质透明,排列成巢状,与丰富的平滑肌瘤样间质混合。患者年龄范围为33至78岁。肿瘤大小为1.5至11厘米。其中6例为男性,9例为女性。在送去进行分子遗传学检测的15个肿瘤中,只有12例可进行分析。所有病例均可进行免疫组织化学分析。在这12例病例中,5例显示完全没有VHL基因突变、VHL高甲基化和3p LOH。在这5例病例中,3例细胞角蛋白7(CK 7)呈阳性。所有5例病例碳酸酐酶9、波形蛋白和CD10均呈阳性。在12例可进行基因分析的病例中,其余7例被发现存在VHL高甲基化、3p LOH、VHL基因突变或前两种特征的组合。这7例病例波形蛋白呈阳性。CK 7、碳酸酐酶9、α-甲基酰基辅酶A消旋酶和CD10的反应性各不相同。在这7例病例中的1例中,发现7号和17号染色体有增益以及VHL基因高甲基化。该病例被认为是伴有7号和17号染色体异常状态的透明细胞肾细胞癌。

结论

(1)平滑肌瘤样间质并非所谓RCCLS所特有。在其他典型的透明细胞肾细胞癌中也可见到。(2)“RCCLS”没有独特的特征性形态学/免疫组织化学特征。(3)我们的结果表明,只有没有VHL基因突变、高甲基化和3p LOH的肿瘤才能被诊断为RCCLS。(4)从我们的研究中,具有显著平滑肌间质的肾细胞癌与肾血管肌腺瘤/透明细胞乳头状(肾小管乳头状)肾细胞癌的关系尚不清楚,必须在更大的患者队列中进一步分析。

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