Torlakovic Emina Emilia, Gomez Jose D, Driman David K, Parfitt Jeremy R, Wang Chang, Benerjee Tama, Snover Dale C
Department of Pathology, Royal University Hospital, University of Saskatchewan, Saskatoon, SK, Canada.
Am J Surg Pathol. 2008 Jan;32(1):21-9. doi: 10.1097/PAS.0b013e318157f002.
The morphologic distinction between various serrated polyps of the colorectum may be challenging. The distinction between sessile serrated adenoma (SSA) and traditional serrated adenoma (TSA) may be difficult using currently available criteria mostly based on cytologic characteristics. We have evaluated 66 serrated polyps including 29 SSA, 18 TSA, and 19 hyperplastic polyps for overall shape of the polyps, architectural features of individual crypts, the presence of eosinophilic cytoplasm, size and distribution of the proliferation and maturation zones, as well as Ki-67 and CK20 expression. The extent of the expression of CK20 and Ki-67 could not distinguish between the 3 types of serrated polyps, but the distribution of their expression was very helpful and differences were statistically significant. The distribution of Ki-67+ cells was the single most helpful distinguishing feature of the serrated polyp type (P<0.0001, chi test). Hyperplastic polyps had regular, symmetric, and increased Ki-67 expression. SSA had irregular, asymmetric, and highly variable expression of Ki-67. TSA had low Ki-67 expression, which was limited to "ectopic crypts" and admixed tubular adenomalike areas. In serrated polyps, ectopic crypt formation (ECF) defined by the presence of ectopic crypts with their bases not seated adjacent to the muscularis mucosae was nearly exclusive to TSA and was found in all cases, while the presence of cytologic atypia and eosinophilia of the cytoplasm were characteristic, but not limited to TSA. No evidence of ECF, but nevertheless abnormal distribution of proliferation zone was characteristic of SSA, whereas HP had neither. The presence of the ECF defines TSA in a more rigorous fashion than previous diagnostic criteria and also explains the biologic basis of exuberant protuberant growth associated with TSA and the lack of such growth in SSA. Recognition of this phenomenon may also help in exploring the genetic and molecular basis for differences between SSA and TSA, because these architectural abnormalities may well be a reflection of abnormalities in genetically programmed mucosal development.
结直肠不同类型锯齿状息肉之间的形态学区分可能具有挑战性。使用目前主要基于细胞学特征的现有标准,很难区分无蒂锯齿状腺瘤(SSA)和传统锯齿状腺瘤(TSA)。我们评估了66个锯齿状息肉,包括29个SSA、18个TSA和19个增生性息肉,观察息肉的整体形状、单个隐窝的结构特征、嗜酸性细胞质的存在、增殖和成熟区的大小及分布,以及Ki-67和CK20的表达。CK20和Ki-67的表达程度无法区分这三种类型的锯齿状息肉,但其表达分布非常有帮助,且差异具有统计学意义。Ki-67+细胞的分布是区分锯齿状息肉类型最有用的单一特征(P<0.0001,卡方检验)。增生性息肉的Ki-67表达规则、对称且增加。SSA的Ki-67表达不规则、不对称且高度可变。TSA的Ki-67表达较低,仅限于“异位隐窝”和混合性管状腺瘤样区域。在锯齿状息肉中,由基部不与黏膜肌层相邻的异位隐窝的存在所定义的异位隐窝形成(ECF)几乎仅见于TSA,且在所有病例中均有发现,而细胞学异型性和细胞质嗜酸性是其特征,但不限于TSA。没有ECF的证据,但增殖区分布异常是SSA的特征,而增生性息肉两者均无。ECF的存在比以往诊断标准更严格地定义了TSA,也解释了与TSA相关的旺盛突出生长以及SSA中缺乏这种生长的生物学基础。认识到这一现象可能也有助于探索SSA和TSA之间差异的遗传和分子基础,因为这些结构异常很可能反映了基因编程的黏膜发育异常。