Wheeler D A, Edmondson H A
Cancer. 1985 Sep 15;56(6):1434-45. doi: 10.1002/1097-0142(19850915)56:6<1434::aid-cncr2820560635>3.0.co;2-f.
This study of 17 cases describes a homogeneous clinicopathologic group of tumors previously subsumed under the general term, hepatobiliary cystadenoma. This unique group of neoplasms that the authors have termed "cystadenoma with mesenchymal stroma" (CMS), occurred exclusively in women and showed two essential tumor components: a cyst lining of columnar to cuboidal, mucin secreting epithelium; and a moderately to densely cellular stroma composed of spindle (rarely oval) cells. The stromal element appeared similar to primitive mesenchyme, both on light and electron microscopic study, showing variable differentiation toward fibroblasts, smooth muscle, adipose tissue and capillaries. Cases of hepatobiliary "cystadenoma" in the literature with histology similar to CMS had similar sex and age incidences, while histologically dissimilar cases, lacking the mesenchymal stroma, had significantly different parameters. Four cases of CMS in this series showed malignant change that was manifested as papillary adenocarcinoma, suggesting the need for complete surgical removal of these premalignant neoplasms.
这项对17例病例的研究描述了一组以前被归入“肝胆管囊腺瘤”这一统称下的具有相同临床病理特征的肿瘤。作者将这一独特的肿瘤组称为“伴有间充质基质的囊腺瘤”(CMS),仅发生于女性,具有两个基本的肿瘤成分:由柱状至立方形、分泌黏液的上皮构成的囊肿内衬;以及由梭形(很少为椭圆形)细胞组成的中度至密集细胞性基质。在光镜和电镜研究中,基质成分看起来类似于原始间充质,显示出向成纤维细胞、平滑肌、脂肪组织和毛细血管的不同程度分化。文献中组织学与CMS相似的肝胆“囊腺瘤”病例具有相似的性别和年龄发病率,而组织学不同、缺乏间充质基质的病例则有显著不同的参数。该系列中的4例CMS显示出恶性变化,表现为乳头状腺癌,提示需要对这些癌前肿瘤进行完整的手术切除。