Völker Hans-Ullrich, Zettl Andreas, Schön Georg, Heller Vitus, Heinrich Elmar, Rosenwald Andreas, Handwerker Mathias, Müller-Hermelink Hans-Konrad, Marx Alexander, Ströbel Philipp
Institute of Pathology, University of Würzburg, Josef-Schneider-Strasse 2, 97080 Würzburg, Germany.
Virchows Arch. 2008 Apr;452(4):457-63. doi: 10.1007/s00428-008-0583-z. Epub 2008 Feb 12.
The current World Health Organization classification recommends the usage of the term sarcomatoid carcinoma (SC) for all biphasic malignant neoplasms of the urinary tract exhibiting morphologic and/or immunohistochemical evidence of epithelial and mesenchymal differentiation. While most SC have been described in the urinary bladder, ureteral SC are extremely rare tumors. Here, we report on the clinical, morphological, and molecular biological findings of two cases in this unusual location. The genetic alterations investigated by comparative genomic hybridization in the epithelial and the mesenchymal component of both cases showed considerable but not complete overlap. Moreover, in spite of many morphological differences between the two cases, both cases shared some genetic gains and losses. Our findings are compatible with the concept that SC originates from a common pluripotent progenitor cell with a potential for epithelial and mesenchymal differentiation.
世界卫生组织目前的分类建议,对于所有表现出上皮和间充质分化的形态学和/或免疫组织化学证据的双相性泌尿系统恶性肿瘤,使用肉瘤样癌(SC)这一术语。虽然大多数SC已在膀胱中被描述,但输尿管SC是极其罕见的肿瘤。在此,我们报告了在这个不寻常部位的两例病例的临床、形态学和分子生物学发现。通过比较基因组杂交在两例病例的上皮和间充质成分中研究的基因改变显示出相当大但不完全重叠。此外,尽管两例病例之间存在许多形态学差异,但两例病例都有一些共同的基因增益和缺失。我们的发现与SC起源于具有上皮和间充质分化潜能的共同多能祖细胞这一概念相符。