Department of Pathology, Stanford University, Stanford, CA, USA.
Am J Surg Pathol. 2009 Oct;33(10):1425-39. doi: 10.1097/PAS.0b013e3181af6067.
The classification and nomenclature of appendiceal mucinous neoplasms are controversial. To determine the outcome for patients with appendiceal mucinous neoplasms and further evaluate whether they can be stratified into groups that provide prognostic information, the clinicopathologic features of 116 patients (66 with clinical follow-up) with appendiceal mucinous neoplasms were studied. From a wide variety of histopathologic features assessed, the important predictors that emerged on univariate statistical analysis were presence of extra-appendiceal neoplastic epithelium (P=0.01), high-grade cytology (P<0.0001), architectural complexity (P<0.001), and invasion (P<0.001). Stratification using a combination of these predictors resulted in a 4-tiered classification scheme. All 16 patients with mucinous neoplasms confined to the appendix and lacking high-grade cytology, architectural complexity, and invasion were alive with no recurrences at median 59 months follow-up (=mucinous adenoma). One of 14 patients with low-grade cytology and acellular peritoneal mucin deposits developed recurrent tumor within the peritoneum at 45 months with no patient deaths to date (median, 48-mo follow-up) (=low-grade mucinous neoplasm with low risk of recurrence). None of the 2 patients with acellular peritoneal mucinous deposits outside of the right lower quadrant developed recurrence at 163 and 206 months. Twenty-seven patients with low-grade mucinous neoplasms with extra-appendiceal neoplastic epithelium had 1-year, 3-year, 5-year, and 10-year overall survival rates of 96%, 91%, 79%, and 46%, respectively, at median 53 months follow-up (=low-grade mucinous neoplasm with high risk of recurrence). Three of the 4 patients with extra-appendiceal epithelium limited to the right lower quadrant developed full-blown peritoneal disease at 6, 41, and 99 months follow-up and 1 patient eventually died of disease. Nine patients with appendiceal neoplasms with invasion or high-grade cytology and follow-up showed 1-year, 3-year, and 5-year overall survival rates of 86%, 57%, and 28% (=mucinous adenocarcinoma). At 10 years, all patients with mucinous adenocarcinoma were either dead or lost to follow-up. Appendiceal mucinous neoplasms can be stratified into 4 distinct risk groups on the basis of a careful histopathologic assessment of cytoarchitectural features and extent of disease at presentation.
阑尾黏液性肿瘤的分类和命名存在争议。为了确定阑尾黏液性肿瘤患者的预后,并进一步评估它们是否可以分为提供预后信息的组,对 116 例阑尾黏液性肿瘤患者(66 例有临床随访)的临床病理特征进行了研究。在评估了广泛的组织病理学特征后,单因素统计分析中出现的重要预测因素是阑尾外肿瘤上皮的存在(P=0.01)、高级别细胞学(P<0.0001)、结构复杂性(P<0.001)和侵袭(P<0.001)。使用这些预测因素的组合进行分层导致了一个 4 级分类方案。所有 16 例局限于阑尾且缺乏高级别细胞学、结构复杂性和侵袭的黏液性肿瘤患者均存活,无复发,中位随访时间为 59 个月(=黏液性腺瘤)。14 例低级别细胞学和无细胞腹膜黏液沉积患者中,1 例在 45 个月时腹膜内复发,但无患者死亡(中位随访时间 48 个月)(=低级别黏液性肿瘤,复发风险低)。无细胞腹膜黏液沉积位于右下象限外的 2 例患者在 163 和 206 个月时无复发。27 例阑尾低级别黏液性肿瘤伴阑尾外肿瘤上皮的患者,中位随访时间为 53 个月,1 年、3 年、5 年和 10 年总生存率分别为 96%、91%、79%和 46%(=低级别黏液性肿瘤,复发风险高)。4 例局限于右下象限的阑尾外上皮患者中有 3 例在 6、41 和 99 个月随访时发展为完全腹膜疾病,1 例患者最终死于疾病。9 例有侵袭或高级别细胞学和随访的阑尾肿瘤患者的 1 年、3 年和 5 年总生存率分别为 86%、57%和 28%(=黏液性腺癌)。10 年时,所有黏液性腺癌患者均死亡或失访。基于对肿瘤细胞结构和发病时疾病范围的仔细组织病理学评估,阑尾黏液性肿瘤可分为 4 个不同的风险组。