Department of Pathology, National University Hospital, Singapore.
Ospedale Pediatrico Bambino Gesu, 00165 Rome, Italy.
Hum Pathol. 2024 Jul;149:55-65. doi: 10.1016/j.humpath.2024.06.007. Epub 2024 Jun 12.
Histological subtyping of hepatocellular carcinoma (HCC) is challenging in the presence of histological heterogeneity, where distinctly different morphological patterns are present within the same tumor. Current approaches rely on percent cut-offs. We hypothesized that morphologic intratumor heterogeneity is a non-random biological feature and that incorporating recurrent patterns would improve histological subtyping of HCC. Resected HCC were studied and the overall frequency of morphologic intratumor heterogeneity was 45% in 242 specimens. Steatohepatitic HCC (SH-HCC) had the highest frequency of morphologic intratumor heterogeneity (91%); this was confirmed in additional cohorts of SH-HCC from different medical centers (overall frequency of 78% in SH-HCC). Morphologic intratumor heterogeneity in SH-HCC showed distinct and recurrent patterns that could be classified as early, intermediate, and advanced. Incorporating these patterns into the definition of SH-HCC allowed successful resolution of several persistent challenges: the problem of the best cut-off for subtyping SH-HCC, the problem of the relationship between SH-HCC and scirrhous HCC, and the classification for HCC with abundant microvesicular steatosis. This approach also clarified the relationship between SH-HCC and CTNNB1 mutations, showing that CTNNB1 mutations occur late in a subset of SH-HCC. In summary, there is a high frequency of morphologic intratumor heterogeneity in HCC. Incorporating this finding into histological subtyping resolved several persistent problems with the SH-HCC subtype.
肝细胞癌 (HCC) 的组织学亚型分类具有挑战性,因为在同一肿瘤中存在明显不同的形态模式,存在组织学异质性。目前的方法依赖于百分比截断值。我们假设形态学肿瘤内异质性是非随机的生物学特征,并且纳入反复出现的模式将改善 HCC 的组织学亚型分类。研究了切除的 HCC,在 242 个标本中,形态学肿瘤内异质性的总体频率为 45%。脂肪性肝炎相关 HCC (SH-HCC) 的形态学肿瘤内异质性频率最高(91%);这在来自不同医疗中心的额外 SH-HCC 队列中得到了证实(SH-HCC 的总体频率为 78%)。SH-HCC 中的形态学肿瘤内异质性表现出明显且反复出现的模式,可以分为早期、中期和晚期。将这些模式纳入 SH-HCC 的定义中,成功解决了几个持续存在的挑战:SH-HCC 亚型分类的最佳截断值问题、SH-HCC 与硬癌性 HCC 之间关系的问题以及富含微泡脂肪变性的 HCC 的分类问题。这种方法还澄清了 SH-HCC 与 CTNNB1 突变之间的关系,表明 CTNNB1 突变发生在 SH-HCC 的一部分中较晚。总之,HCC 中存在较高频率的形态学肿瘤内异质性。将这一发现纳入组织学亚型分类中,解决了 SH-HCC 亚型的几个持续存在的问题。