Iwaya T, Maesawa C, Uesugi N, Kimura T, Ogasawara S, Ikeda K, Kimura Y, Mitomo S, Ishida K, Sato N, Saito K, Masuda T
Department of Surgery I, Iwate Medical University School of Medicine, Morioka, Japan.
Dis Esophagus. 2006;19(1):48-52. doi: 10.1111/j.1442-2050.2006.00538.x.
Most esophageal carcinosarcomas are diagnosed as so-called carcinosarcoma, in which individual elements may be derived from a single common ancestor cell, and there have been a few reports describing true carcinosarcoma originating from two individual stem cells. We describe a case of esophageal carcinosarcoma exhibiting neoplastic osteoid formation. Immunoreactivity for vimentin and p53 was limited to only the sarcomatous component and was absent in the carcinomatous component. Furthermore, a point mutation in exon 7 of the p53 gene was observed only in the sarcomatous component. Both sarcoma and carcinoma cells distinctively metastasized to different lymph nodes. These observations led us to diagnose the esophageal tumor as a true carcinosarcoma.
大多数食管癌肉瘤被诊断为所谓的癌肉瘤,其中各个成分可能源自单个共同的祖细胞,并且有一些报告描述了源自两个独立干细胞的真正癌肉瘤。我们描述了一例表现出肿瘤性类骨质形成的食管癌肉瘤病例。波形蛋白和p53的免疫反应性仅局限于肉瘤成分,而在癌成分中不存在。此外,仅在肉瘤成分中观察到p53基因第7外显子的点突变。肉瘤细胞和癌细胞分别转移至不同的淋巴结。这些观察结果使我们将该食管肿瘤诊断为真正的癌肉瘤。