Guarino M, Tricomi P, Giordano F, Cristofori E
Department of Anatomical Pathology, Hospital of Vimercate, Italy.
Pathology. 1996 Nov;28(4):298-305. doi: 10.1080/00313029600169224.
Malignant tumors with a mixed phenotype are a controversial field of pathology. In this article the morphological aspects and the immunohistological characterization of sarcomatoid carcinomas are presented. These uncommon neoplasms show both carcinomatous and sarcomatous features, and have been described in the past under a variety of different names causing great uncertainty about their classification and histogenesis. They can occur in various anatomical sites and exhibit a wide range of microscopic appearances, but some features are quite characteristic and are found in many cases. Morphological "transition" between carcinomatous and sarcomatous tissue, and detection of epithelial characteristics by electron microscopy or immunohistochemistry in the sarcomatous component, are very peculiar features of these neoplasms, providing both helpful clues for pathological diagnosis and important insights into histogenesis. Here a unifying histopathogenetic mechanism based on the phenotypic conversion of carcinoma into sarcomatoid tissue is proposed and supporting literature data from both experimental systems and clinicopathological observations are reviewed and discussed.
具有混合表型的恶性肿瘤是病理学中一个存在争议的领域。本文介绍了肉瘤样癌的形态学特征和免疫组织化学特征。这些罕见的肿瘤同时具有癌性和肉瘤性特征,过去曾以多种不同的名称进行描述,这使得它们的分类和组织发生存在很大的不确定性。它们可发生于各种解剖部位,呈现出广泛的微观表现,但有些特征非常典型,在许多病例中都能发现。癌性组织和肉瘤性组织之间的形态学“过渡”,以及通过电子显微镜或免疫组织化学在肉瘤成分中检测到上皮特征,是这些肿瘤非常独特的特征,为病理诊断提供了有用的线索,并对组织发生有重要的启示。本文提出了一种基于癌向肉瘤样组织表型转化的统一组织病理学发生机制,并对来自实验系统和临床病理观察的支持性文献数据进行了综述和讨论。