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Unique case of caecum plasmablastic lymphoma CD138(+) in patient with late diagnosed colon neuroendocrine carcinoma
Authors:Foltyn Wanda  Kos-Kudła Beata  Siemińska Lucyna  Zemczak Anna  Strzelczyk Janusz  Marek Bogdan  Kajdaniuk Dariusz  Nowak Mariusz  Borowska Małgorzata  Jurecka-Lubienicka Beata
Affiliation:Division of Endocrinology, Department of Pathophysiology and Endocrinology, Zabrze, Medical University of Silesia, Katowice. wandafoltyn@poczta.onet.pl
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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