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唾液腺黏液表皮样癌是一种临床上、形态学上和遗传学上具有异质性的实体:40 例病例的临床病理研究,重点是分级、组织学变异和 t(11;19)易位的存在。

Salivary gland mucoepidermoid carcinoma is a clinically, morphologically and genetically heterogeneous entity: a clinicopathological study of 40 cases with emphasis on grading, histological variants and presence of the t(11;19) translocation.

机构信息

Department of Pathology, University of Erlangen, Erlangen, Germany.

出版信息

Histopathology. 2011 Mar;58(4):557-70. doi: 10.1111/j.1365-2559.2011.03777.x. Epub 2011 Mar 3.

DOI:10.1111/j.1365-2559.2011.03777.x
PMID:21371076
Abstract

AIMS

To correlate World Health Organization (WHO) grade, patient's outcome and presence of t(11;19) to histological tumour variants in 40 well-characterized mucoepidermoid carcinomas (MECs).

METHODS AND RESULTS

MECs were classified as 'classical' based on the presence of equal proportions of the three cell types or the dominance (≥50%) of mucous cells together with at least one other cell type, and as 'variant' if composed of ≥80% of a single non-mucous cell type. Classical MECs were more common (n=23). Variant MECs had predominant squamoid (n=9), eosinophilic (n=5) or clear cell (n=3) morphology. Twenty-seven tumours were WHO grade 1, three grade 2 and ten grade 3. The t(11;19) was detected in 82%, 35% and 0% of classical MEC, variant MEC and non-MEC, respectively. Classical MECs were associated significantly with age ≤60 years (P<0.001), grade 1 (P<0.001) and t(11;19) (P=0.003). Short overall survival was associated significantly with age >60 years (P=0.001) and Union for International Cancer Control (UICC) stage >I (P=0.031), residual tumour (P<0.001), tumour grade >1 (P=0.001) and squamoid variant (P=0.002) in Kaplan-Meier analysis.

CONCLUSIONS

The results underscore the great histological diversity of MEC, the reproducibility of the WHO grading criteria and the value of histological subtypes as an additional prognostic factor.

摘要

目的

在 40 例经过充分特征描述的黏液表皮样癌(MEC)中,将世界卫生组织(WHO)分级、患者结局和 t(11;19)与组织学肿瘤变体相关联。

方法和结果

MEC 根据三种细胞类型的比例相等或黏液细胞占主导地位(≥50%)并至少有另一种细胞类型来分类为“经典型”,如果由≥80%的单一非黏液细胞类型组成,则分类为“变体型”。经典型 MEC 更为常见(n=23)。变体 MEC 具有明显的鳞状(n=9)、嗜酸性粒细胞(n=5)或透明细胞(n=3)形态。27 个肿瘤为 WHO 分级 1 级,3 个为 2 级,10 个为 3 级。t(11;19)在经典型 MEC、变体型 MEC 和非 MEC 中的检出率分别为 82%、35%和 0%。经典型 MEC 与年龄≤60 岁(P<0.001)、分级 1(P<0.001)和 t(11;19)(P=0.003)显著相关。总生存时间较短与年龄>60 岁(P=0.001)和国际抗癌联盟(UICC)分期>1 期(P=0.031)、残余肿瘤(P<0.001)、肿瘤分级>1 级(P=0.001)和鳞状变体(P=0.002)显著相关。

结论

这些结果强调了 MEC 具有很大的组织学多样性,WHO 分级标准具有可重复性,并且组织学亚型作为附加预后因素具有价值。

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