نتایج جستجو برای: q21

تعداد نتایج: 1024  

Journal: :Annals of oncology : official journal of the European Society for Medical Oncology 2010
M Paulli L Arcaini M Lucioni E Boveri D Capello F Passamonti M Merli S Rattotti D Rossi R Riboni E Berti U Magrini R Bruno G Gaidano M Lazzarino

BACKGROUND Hepatitis C virus (HCV) infection has been linked to lymphoproliferative disorders. Marginal zone B-cell lymphoma (MZL) represents one of the most frequent lymphoma subtypes associated with HCV infection. We describe an unusual subset of HCV-associated MZL characterized by subcutaneous presentation. MATERIALS AND METHODS A series of 12 HCV-positive patients presenting with subcutan...

2004
Liza Ho R. Eric Davis Béatrice Conne Richard Chappuis Margaret Berczy Paulette Mhawech Louis M. Staudt Juerg Schwaller

The most frequently recurring translocations in mucosa-associated lymphoid tissue (MALT) B-cell non-Hodgkin lymphoma, t(11;18)(q21;q21) and t(14;18)(q32; q21), lead to formation of an API2-MALT1 fusion or IgH-mediated MALT1 overexpression. Various approaches have implicated these proteins in nuclear factor B (NFB) signaling, but this has not been shown experimentally in human B cells. Immunohis...

Journal: :Journal of clinical and experimental hematopathology : JCEH 2013
Rie Tabata Ryoji Yasumizu Chiharu Tabata Masaru Kojima

Here, we report a rare case of double-hit lymphoma, demonstrating t(6;14;18)(p25;q32;q21), suggesting two independent dual-translocations, c-MYC/BCL-2 and IRF4/BCL-2. The present case had a rare abnormal chromosome, t(6;14;18)(p25;q32;q21), independently, in addition to known dual-hit chromosomal abnormalities, t(14;18)(q32;q21) and t(8;22)(q24;q11.2). Lymph node was characterized by a follicul...

Journal: :The Korean journal of laboratory medicine 2010
Ji Eun Kim Kwang Sook Woo Kyung Eun Kim Sung Hyun Kim Joo In Park Lisa G Shaffer Jin Yeong Han

Patients with ALL rarely present with t(12;17)(p13;q21) as the primary clonal abnormality; this abnormality is associated with the expression of myeloid antigens. In this study, we have reported presumably the first case of this chromosomal abnormality in Korea, thereby facilitating the delineation of a distinct subtype of ALL. A 57-yr-old woman was referred to our hospital because of pancytope...

Journal: :Blood 2014
Mario Acunzo Giulia Romano Dorothee Wernicke Veronica Balatti Laura Z Rassenti Marie dell'Aquila Thomas J Kipps Yuri Pekarsky Carlo M Croce

Recent investigations of chromosomal aberrations in chronic lymphocytic leukemia (CLL) led to a better understanding of the molecular causes of CLL. Here we report a rearrangement between MAML2 (mastermind-like protein 2) and CXCR4 (specific receptor for CXC chemokine stromal cell-derived factor-1) in CLL cells of a patient with a t(2;11)(q22.1;q21) chromosomal translocation. The rearrangement ...

Journal: :The Journal of clinical investigation 2006
Francesco Bertoni Emanuele Zucca

Mucosa-associated lymphoid tissue (MALT) lymphomas can arise in a variety of extranodal sites. Interestingly, at least 3 different, apparently site-specific, chromosomal translocations, all affecting the NF-kappaB pathway, have been implicated in the development and progression of MALT lymphoma. The most common is the translocation t(11;18)(q21;q21), which results in a fusion of the cIAP2 regio...

2011
Xiao Min Zhang Na Liu Yanan Li Chunrui

Acute megakaryoblastic leukemia (AMKL) is a type of acute myeloid leukemia (AML), in which majority of the blasts are megakaryoblastic. De novo AMKL in adulthood is rare, and carries very poor prognosis. We here report a 45-year-old woman with de novo AMKL with BCR/ABL rearrangement and der(16)t(1;16)(q21;q23) translocation but negative for t(9;22) Ph chromosome. Upon induction chemotherapy con...

Journal: :Blood 1989
E G Levine D C Arthur J Machnicki G Frizzera D Hurd B Peterson K J Gajl-Peczalska C D Bloomfield

The identification of recurring chromosomal translocations has provided clues to the gene regions important in lymphoma development. Among 157 patients with non-Hodgkin lymphoma studied by cytogenetic analysis, four new recurring translocations have been identified--t(8;9) (q24;p13), t(11;18)(q21;q21), t(14,15)(q32;q15), and an unbalanced translocation giving rise to der(22)t(17;22) (q11;p11). ...

2016
Laura E Brown Da Zhang Diane L Persons Abdulraheem Yacoub Shivani Ponnala Wei Cui

Various translocations involving the PDGFRB gene are identified in myeloid neoplasms. However, the PRKG2/PDGFRB fusion gene associated with t(4;5)(q21;q33) has previously been reported in only 3 patients. We present the case of a 26-year-old woman with microcytic anemia, basophilia, thrombocytosis, and massive splenomegaly, who was found to have systemic mastocytosis and associated clonal hemat...

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