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ARTICLE

Merkel Cell Carcinoma: A Rare Cause of Hypervascular Nasal Tumor

Louisa Azizia, Kathlyn Marsot-Dupucha, Pascal Bigela, Samy Mzalia, Bernard Meyera and Jean Michel Tubianaa

a From the Departments of Radiology (L.A., K.M.-D., J.M.T.), Anatomo-pathology (P.B.), and Otolaryngology (S.M., B.M.), Hopital Saint Antoine, Paris, France.

Summary: Cutaneous neuroendocrine carcinoma, first described in 1972, is an aggressive disease usually occurring in sun-exposed skin. Other sites have been described, however; such tumors occasionally occur within the nasal fossa. A high rate of metastasis (>30%) explains the poor prognosis. Descriptions of the imaging features of these tumors, mainly located in cutaneous region, are rare. We therefore present the imaging features of two cases of Merkel cell carcinoma involving the sinonasal region, suggestive of a hypervascular tumor.




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S. E. Anderson, K. T. Beer, A. Banic, L. S. Steinbach, M. Martin, E. E. Friedrich, E. Stauffer, P. Vock, and R. H. Greiner
MRI of Merkel Cell Carcinoma: Histologic Correlation and Review of the Literature
Am. J. Roentgenol., December 1, 2005; 185(6): 1441 - 1448.
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