Unique case of caecum plasmablastic lymphoma CD138(+) in patient with late diagnosed colon neuroendocrine carcinoma |
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Authors: | Foltyn Wanda Kos-Kudła Beata Siemińska Lucyna Zemczak Anna Strzelczyk Janusz Marek Bogdan Kajdaniuk Dariusz Nowak Mariusz Borowska Małgorzata Jurecka-Lubienicka Beata |
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Affiliation: | Division of Endocrinology, Department of Pathophysiology and Endocrinology, Zabrze, Medical University of Silesia, Katowice. wandafoltyn@poczta.onet.pl |
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Abstract: | Neuroendocrine tumors are frequently associated with other primary malignancies. Plasmablastic lymphoma is a rare, aggressive neoplasm, derived from large B-cell, associated with human immunodeficiency virus infection. Plasmablastic lymphoma cells share many cytomorphologic and immunophenotypic features with plasmablastic cells, causing some diagnostic problems. We present a unique case of coexisting two very uncommon neoplasms: plasmablastic lymphoma and neuroendocrine carcinoma in 54-years-old men. This is the first report of caecum localization of plasmablastic lymphoma. Presented case images diagnostic problems in rare neoplasms. |
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