Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA.
Hum Pathol. 2013 Jul;44(7):1293-9. doi: 10.1016/j.humpath.2012.10.017. Epub 2013 Jan 21.
SALL4 is a transcription factor that serves as a marker of yolk sac tumor. Yolk sac tumor and hepatocellular carcinoma share histologic, serologic, and immunohistochemical features. Previous studies have shown lack of SALL4 expression in hepatocellular carcinoma, suggesting utility in this differential diagnosis. Sixty-nine samples of hepatocellular carcinoma were retrieved from surgical pathology archives and used to construct 9 tissue microarrays. A germ cell tumor tissue microarray containing 10 yolk sac tumors was used for comparison. Extent, intensity, and pattern of nuclear SALL4 expression were assessed in each spot. Mean percentage of expression was calculated for each tumor and used during analysis. Optimal discriminatory extent of expression cutoff was determined by receiver operating characteristic curve analysis. Other potential discriminatory markers including Hep Par1 were also evaluated. Forty-six percent (32/69) of hepatocellular carcinoma and all yolk sac tumors revealed at least focal expression of SALL4. A unique punctuate/clumped pattern of nuclear staining was present in 94% (30/32) of hepatocellular carcinoma, whereas all yolk sac tumors displayed a diffuse finely granular nuclear staining pattern. A 25% extent of SALL4 expression cutoff was found to be optimal for the distinction of yolk sac tumor from hepatocellular carcinoma yielding a sensitivity of 100%, specificity of 92.8%, and a positive predictive value of 66.6% for yolk sac tumor diagnosis. The addition of Hep Par1 increased the specificity (99%) and positive predictive value (90%). This is the first report of SALL4 expression in hepatocellular carcinoma. Our finding should be taken into consideration in the differential diagnosis of hepatocellular carcinoma and yolk sac tumor. The unique punctuate/clumped pattern seen in hepatocellular carcinoma cases could be of further discriminatory value.
SALL4 是一种转录因子,作为卵黄囊肿瘤的标志物。卵黄囊肿瘤和肝细胞癌具有组织学、血清学和免疫组织化学特征。先前的研究表明 SALL4 在肝细胞癌中表达缺失,提示在这种鉴别诊断中具有应用价值。从外科病理学档案中检索了 69 例肝细胞癌样本,并用于构建 9 个组织微阵列。使用包含 10 个卵黄囊肿瘤的生殖细胞肿瘤组织微阵列进行比较。评估了每个点的核 SALL4 表达的程度、强度和模式。计算了每个肿瘤的平均表达百分比,并在分析中使用。通过接收者操作特征曲线分析确定最佳的表达截断范围以进行区分。还评估了其他潜在的鉴别标记物,包括 Hep Par1。46%(32/69)的肝细胞癌和所有卵黄囊肿瘤均至少局灶性表达 SALL4。94%(30/32)的肝细胞癌存在独特的点状/块状核染色模式,而所有卵黄囊肿瘤均显示弥漫性细颗粒状核染色模式。发现 25%的 SALL4 表达截断值可最佳地区分卵黄囊肿瘤和肝细胞癌,卵黄囊肿瘤的诊断敏感性为 100%,特异性为 92.8%,阳性预测值为 66.6%。添加 Hep Par1 可提高特异性(99%)和阳性预测值(90%)。这是 SALL4 在肝细胞癌中表达的首次报道。我们的发现应在肝细胞癌和卵黄囊肿瘤的鉴别诊断中加以考虑。在肝细胞癌病例中观察到的独特点状/块状模式可能具有进一步的鉴别价值。