Ectomesenchymal chondromyxoid tumor: Histopathologic and immunohistochemical study of two cases without a chondroid component

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Abstract

Ectomesenchymal chondromyxoid tumor (ECT) is a rare benign neoplasm usually affecting the anterior dorsum of the tongue. Histopathologically, it is formed by spindle, round and/or polygonal cells embedded in a chondromyxoid matrix. Immunohistochemical positivity for vimentin, S-100 protein, glial fibrillary acid protein and neuron-specific enolase are helpful to confirm the diagnosis. There are 42 cases of ECT of the tongue reported in the English language literature, three of them showing no chondroid matrix. We describe two additional cases of ECT lacking the chondroid component, exhibiting areas of reticulated myxoid and cellular pattern. Considering the microscopical features, ECT can be classified in classic and 'chondroid-free' variants, the latter including the reticulated myxoid and cellular patterns. It is important to consider that the cellular ECT usually exhibits predominance of an infiltrative atypical cellular component that may mimic a malignant tumor. Copyright © 2012 John Wiley & Sons A/S.

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Palma Guzmán, J. M., De Andrade, B. A. B., Rizo, V. H. T., Romañach, M. J., Leõn, J. E., & De Almeida, O. P. (2012). Ectomesenchymal chondromyxoid tumor: Histopathologic and immunohistochemical study of two cases without a chondroid component. Journal of Cutaneous Pathology, 39(8), 781–786. https://doi.org/10.1111/j.1600-0560.2012.01910.x

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