Literature DB >> 16773592

[Unique case of caecum plasmablastic lymphoma CD138(+) in patient with late diagnosed colon neuroendocrine carcinoma].

Wanda Foltyn1, Beata Kos-Kudła, Lucyna Siemińska, Anna Zemczak, Janusz Strzelczyk, Bogdan Marek, Dariusz Kajdaniuk, Mariusz Nowak, Małgorzata Borowska, Beata Jurecka-Lubienicka.   

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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Year:  2006        PMID: 16773592

Source DB:  PubMed          Journal:  Endokrynol Pol        ISSN: 0423-104X            Impact factor:   1.582


  1 in total

1.  Simultaneous occurrence of colonic adenocarcinoma and MALT lymphoma: A series of three cases.

Authors:  Theodoros Argyropoulos; Periklis Foukas; Maria Kefala; Panagiotis Xylardistos; Sotirios Papageorgiou; Nikolaos Machairas; Evmorfia Boltetsou; Anastasios Machairas; Ioannis G Panayiotides
Journal:  World J Gastrointest Oncol       Date:  2012-04-15
  1 in total

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