Treatment of synchronous mantle cell lymphoma and small lymphocytic lymphoma with bendamustine and rituximab.

Abstract:

:Herein, we describe a case of a female patient in whom B cell chronic lymphocytic leukemia (CLL) and mantle cell lymphoma (MCL) were diagnosed simultaneously. She presented with anemia, thrombocytopenia and splenomegaly. Flow cytometry demonstrated two immunophenotypically distinct CD5-positive monoclonal B cell populations. Peripheral blood fluorescence in situ hybridization (FISH) was positive for IGH/CCND1, consistent with t(11;14) translocation. She received 6 cycles of bendamustine 70 mg/m(2)/day for 2 days and rituximab on the first day every 4 weeks along with granulocyte-colony stimulating factor. She had an excellent response, and repeat computed tomography after her third cycle of chemotherapy revealed no organomegaly or lymphadenopathy. Her peripheral blood lymphocytosis also resolved. Bone marrow examination revealed no detectable flow-cytometric evidence of MCL or CLL. Repeat cytogenetic and FISH analysis were also normal. The patient remains in complete remission 20 months after her initial diagnosis and is receiving maintenance rituximab 375 mg/m(2) weekly for 4 weeks every 6 months for 2 years.

journal_name

Acta Haematol

journal_title

Acta haematologica

authors

Kourelis TV,Kahl BS,Benn P,Delach JA,Bilgrami SF

doi

10.1159/000324193

subject

Has Abstract

pub_date

2011-01-01 00:00:00

pages

40-3

issue

1

eissn

0001-5792

issn

1421-9662

pii

000324193

journal_volume

126

pub_type

杂志文章
  • Fluorescence in situ hybridization and surface markers of fine needle aspiration specimen confirm extramedullary myeloblastoma in a patient with chronic myeloid leukemia.

    abstract::We report on a patient with chronic myeloid leukemia (CML) with a rapidly growing left cervical tumor 5 months after the initial diagnosis of CML. This tumor was diagnosed as a very early manifestation of extramedullary myeloblastoma by a minimally invasive method. A fine needle aspirate (26-gauge needle) was obtained...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000040873

    authors: Karthaus M,Meran JG,Wilkens L,Soudah B,Diedrich H,Krauter J,Ganser A,Heil G

    更新日期:1998-01-01 00:00:00

  • Detection of granulocyte-macrophage colony-stimulating factor in cerebrospinal fluid of patients with aseptic meningitis.

    abstract::The level of granulocyte-macrophage colony-stimulating factor (GM-CSF) in the cerebrospinal fluid from 14 infants and children with meningitis and 6 patients who suffered other diseases besides meningitis was measured by our sensitive enzyme linked immunosorbent assay for GM-CSF. The minimal detection level of GM-CSF ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000204796

    authors: Shimoda K,Okamura S,Omori F,Mizuno Y,Hara T,Aoki T,Akeda H,Ueda K,Niho Y

    更新日期:1991-01-01 00:00:00

  • Autophagic Markers BECLIN 1 and LC3 are Associated with Prognosis of Multiple Myeloma.

    abstract:BACKGROUND/AIMS:Autophagy is crucial for the survival and function of plasma cells including protection from toxic misfolded immunoglobulin and proper energy metabolism. Multiple myeloma (MM) is an indolent but eventually fatal neoplasm of plasma cells. Autophagy may play a critical role in the survival of MM cells and...

    journal_title:Acta haematologica

    pub_type: 临床试验,杂志文章

    doi:10.1159/000368848

    authors: Jung G,Roh J,Lee H,Gil M,Yoon DH,Suh C,Jang S,Park CJ,Huh J,Park CS

    更新日期:2015-01-01 00:00:00

  • Bone marrow fibroblasts in acute lymphoblastic leukemia.

    abstract::Fibroblast-like cells were grown from the bone marrow of acute lymphoblastic leukemia (ALL) patients before, during and off therapy. A diminished growth capacity was observed in cells from patients before and during therapy. In the three groups studied, differences were also observed in the effect of hydrocortisone on...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206284

    authors: Bruzzone MS,Minguell JJ

    更新日期:1985-01-01 00:00:00

  • Proteomic Profiling of Signaling Networks Modulated by G-CSF/Plerixafor/Busulfan-Fludarabine Conditioning in Acute Myeloid Leukemia Patients in Remission or with Active Disease prior to Allogeneic Stem Cell Transplantation.

    abstract::To characterize intracellular signaling in peripheral blood (PB) cells of acute myeloid leukemia (AML) patients undergoing pretransplant conditioning with CXCR4 inhibitor plerixafor, granulocyte colony-stimulating factor (G-CSF), and busulfan plus fludarabine (Bu+Flu) chemotherapy, we profiled 153 proteins in 33 funct...

    journal_title:Acta haematologica

    pub_type: 临床试验,杂志文章

    doi:10.1159/000495456

    authors: Zeng Z,Liu W,Benton CB,Konoplev S,Lu H,Wang RY,Chen J,Shpall E,Baggerly KA,Champlin R,Konopleva M

    更新日期:2019-01-01 00:00:00

  • Scanning electron microscopic study of leukemic human B lymphocytes.

    abstract::Peripheral blood lymphocytes from patients with chronic lymphocytic leukemia (CLL), lymphoplasmacytoid lymphoma, centrocytic lymphoma and hairy cell leukemia were studied by scanning electron microscopy (SEM). In general, SEM revealed rather homogenous cell populations. Most lymphocytes displayed a moderately villous ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207888

    authors: Fischer K,Cohnen G,Szaniawski W,Brittinger G

    更新日期:1977-03-01 00:00:00

  • A case of lymphoma-type alpha-chain disease.

    abstract::A 69-year-old man with a rare case of lymphoma-type alpha-chain disease was admitted to the hospital with marked cervical and inguinal lymph node swelling. Lymph node biopsy showed marked infiltration of plasma cells, plasmacytoid cells and immunoblastoid cells, alone or in combination. Immunoelectrophoresis and immun...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000204814

    authors: Itoh Y,Ohtaki H,Ono T,Mori N,Kawaoi A,Kawai T

    更新日期:1991-01-01 00:00:00

  • Predictive factors for cure after immunosuppressive therapy of aplastic anemia.

    abstract::In a previous study, we evaluated efficacy of repeated antilymphocyte globulin (ALG) treatment for patients with severe aplastic anemia not responding to an initial ALG treatment or relapsing after initial response to ALG. We now searched in the same cohort of patients for differences between patients who responded to...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000041005

    authors: Viollier R,Tichelli A

    更新日期:2000-01-01 00:00:00

  • The significance of minimal residual disease in stem cell grafts and the role of purging: is it better to purge in vivo or in vitro?

    abstract::Contamination of autologous graft by tumor, in addition to incomplete tumor eradication, can partly explain why relapse remains the commonest cause of treatment failure after autologous stem cell transplantation (ASCT) in patients with malignant hematologic disorders. Monitoring of minimal residual disease (MRD) is no...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000088411

    authors: Melillo L,Cascavilla N,Lerma E,Corsetti MT,Carella AM

    更新日期:2005-01-01 00:00:00

  • Roles of hematopoietic transcription factors GATA-1 and GATA-2 in the development of red blood cell lineage.

    abstract::The transcription factors GATA-1 and GATA-2 play key roles in gene regulation during erythropoiesis. Gene ablation studies in mouse revealed that GATA-2 is crucial for the maintenance and proliferation of immature hematopoietic progenitors, whereas GATA-1 is essential for the survival of erythroid progenitors as well ...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000065660

    authors: Ohneda K,Yamamoto M

    更新日期:2002-01-01 00:00:00

  • Polymorphism of foetal haemoglobin in the Sardinian beta +-thalassaemia.

    abstract::12 thalassaemic patients from Northern Sardinia showing the beta + phenotype were examined by isoelectric focusing and high-performance liquid chromatography techniques for the determination of the variant A gamma T globin chain of the foetal haemoglobin. Two patients (16.7%) were homozygotes for the A gamma T gene va...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206057

    authors: Masala B,Formato M,Manca L,Demuro P,Gallisai D,Dore F,Longinotti M

    更新日期:1986-01-01 00:00:00

  • Blastic plasmacytoid dendritic cell neoplasm without cutaneous lesion at presentation: case report and literature review.

    abstract::Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare and highly aggressive hematological malignancy derived from precursors of plasmacytoid dendritic cells. This disease typically presents with cutaneous involvement as the first manifestation, with subsequent or simultaneous spread to bone marrow and periphe...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000334703

    authors: Wang H,Cao J,Hong X

    更新日期:2012-01-01 00:00:00

  • Alkaline phosphatase-positive leukemic monocytes in a child with acute monocytic leukemia.

    abstract::A subpopulation with alkaline phosphatase activity and neutrophilic granules was found in leukemic monocytes from a child with acute monocytic leukemia (M5B). Almost all leukemic cells were strongly positive for nonspecific esterase and phagocytized opsonized zymosans. These findings suggest that the subpopulation are...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206516

    authors: Tomonaga M,Ichimaru M,Tsuji Y

    更新日期:1984-01-01 00:00:00

  • Probable acenocoumarol-amoxycillin interaction.

    abstract::We present the case of a woman undergoing treatment with acenocoumarol for deep vein thrombosis, who maintained an international normalized ratio (INR) of between 2.5 and 4 for 2 months. Seven days after the introduction of amoxycillin (500 mg/8 h) for a probable respiratory infection, the patient developed spontaneou...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000204457

    authors: Soto J,Sacristan JA,Alsar MJ,Fernandez-Viadero C,Verduga R

    更新日期:1993-01-01 00:00:00

  • Adhesion of human hematopoietic progenitor cells to bone-marrow-derived stromal cells is enhanced by antibodies to CD44.

    abstract::It has been suggested that CD44 mediates adhesive interactions between hematopoietic progenitor cells and the stromal microenvironment. Ligands of CD44 include several extracellular matrix components, such as hyaluronic acid and fibronectin. Antibodies against CD44 have been shown to induce homotypic T cell aggregatio...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000203886

    authors: Oostendorp RA,Spitzer E,Dörmer P

    更新日期:1996-01-01 00:00:00

  • Immunophenotypic analysis of lymphocytes and myeloma cells in patients with multiple myeloma.

    abstract::The immunological phenotypes of lymphocytes and myeloma cells in 48 patients with multiple myeloma (MM) were analyzed using a panel of monoclonal antibodies (mAbs). Myeloma cells were positive for OKT10, BL3, PCA1 and BA2. In a few cases, they were also positive for the B cell-associated antigens J5, B1 and I2. Eight ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000205187

    authors: Shimazaki C,Fried J,Perez AG,Scheinberg DA,Atzpodien J,Wang CY,Wisniewolski R,Clarkson BD

    更新日期:1990-01-01 00:00:00

  • Hematopoietic modulation by the tachykinins.

    abstract::We have been studying hematopoietic effects by the tachykinins, which like many other neuropeptides can be expressed in neural and nonneural tissues. Substance P (SP) and neurokinin-A (NK-A), members of the tachykinins are immune and hematopoietic modulators. SP and NK-A are derived from the preprotachykinin-I gene (P...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000203593

    authors: Rameshwar P,Gascón P

    更新日期:1997-01-01 00:00:00

  • Additional data from two kindreds with genetically induced deficiencies of erythrocyte pyrimidine nucleotidase.

    abstract::Two subjects, not previously reported in detail, had severe inherited deficiencies of erythrocyte pyrimidine nucleotidase. This was manifested hematologically by moderate hemolytic anemia with splenomegaly, morphologically by punctate basophilic stippling of Wright's stained erythrocytes, and biochemically by intraery...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207413

    authors: Paglia DE,Fink K,Valentine WN

    更新日期:1980-01-01 00:00:00

  • Thyroid tumor as initial presentation of Hodgkin's disease: a case report including an immunophenotypic characterization.

    abstract::A rare case of Hodgkin's disease which initially presented with a thyroid tumor in an 18-year-old-man is reported. The tumor involved most of the thyroid gland but was well demarcated, and the border between the tumor and the remnants of the thyroid gland was relatively clear, suggesting secondary Hodgkin's disease in...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000203627

    authors: Nakamura S,Mizukami Y,Yokoyama K,Saito Y,Ohtake S,Matsuda T

    更新日期:1997-01-01 00:00:00

  • Ponatinib in the Treatment of Chronic Myeloid Leukemia and Philadelphia Chromosome-Positive Acute Leukemia: Recommendations of a German Expert Consensus Panel with Focus on Cardiovascular Management.

    abstract::Treatment of chronic myeloid leukemia (CML) and Philadelphia chromosome-positive acute leukemia (Ph+ ALL) has been revolutionized with the advent of tyrosine kinase inhibitors (TKIs). Most patients with CML achieve long-term survival similar to individuals without CML due to treatment with TKIs not only in frontline b...

    journal_title:Acta haematologica

    pub_type: 共识发展会议,杂志文章,评审

    doi:10.1159/000501927

    authors: Saussele S,Haverkamp W,Lang F,Koschmieder S,Kiani A,Jentsch-Ullrich K,Stegelmann F,Pfeifer H,La Rosée P,Goekbuget N,Rieger C,Waller CF,Franke GN,le Coutre P,Kirchmair R,Junghanss C

    更新日期:2020-01-01 00:00:00

  • Cytokine gene expression in regenerating haematopoietic tissues of mice after cyclophosphamide treatment.

    abstract::The goal of the study was to investigate changes in expression of selected growth factors tentatively involved in regeneration of haematopoietic tissues (bone marrow and spleen) following cyclophosphamide (CY) damage in the mouse. The bone marrow (BM) and spleen were examined separately, since the regenerating pattern...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000068490

    authors: Psenák O,Sefc L,Sýkora V,Chang KT,Necas E

    更新日期:2003-01-01 00:00:00

  • Biologic nature of the myelodysplastic syndromes.

    abstract::In the myelodysplastic syndromes (MDS) clonogenic marrow cell culture studies have demonstrated intrinsic hemopoietic stem cell and progenitor cell abnormalities consistent with these disorders representing clonal hemopathies. Abnormal responsiveness of these cells to stimulatory and inhibitory growth factors indicate...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000205911

    authors: Greenberg PL

    更新日期:1987-01-01 00:00:00

  • A glucose-6-phosphate dehydrogenase variant, Gd(-) Santamaria found in Costa Rica.

    abstract::Red cell glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-chromosomal-linked abnormality often associated with hemolytic anemia. The G6PD variants obtained from 2 unrelated males, one associated with enzyme deficiency and history of hemolytic jaundice, and the other associated with enzyme deficiency but no ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206354

    authors: Sáenz GF,Chaves M,Berrantes A,Elizondo J,Montero AG,Yoshida A

    更新日期:1984-01-01 00:00:00

  • Maternal selective serotonin reuptake inhibitor intake does not seem to affect neonatal platelet function tests.

    abstract::Recently, concerns have been raised regarding the potential impairment of neonatal platelet function and the potential risk of bleeding in neonates born to mothers treated with selective serotonin reuptake inhibitors (SSRI). Our aim was to test whether the platelet function of neonates born to SSRI-treated mothers was...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000090929

    authors: Maayan-Metzger A,Kuint J,Lubetsky A,Shenkman B,Mazkereth R,Kenet G

    更新日期:2006-01-01 00:00:00

  • Avascular necrosis of the femoral head in sickle cell syndrome: a report of 5 cases.

    abstract::The course and management of avascular necrosis of the femoral head (AVNFH) in six hips of 5 sickle cell syndrome patients (3 with Hb SS, 1 with Hb SC and 1 with Hb S/beta+-thalassaemia) are described. Two patients (aged 13 and 17 years) presented with Perthes- and osteochondritis dessicans-type lesions. These hips pr...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000205873

    authors: Rand C,Pearson TC,Heatley FW

    更新日期:1987-01-01 00:00:00

  • Autosomal dominant von Willebrand disease type 2M.

    abstract::von Willebrand disease (VWD) type 2M is a distinct entity and clearly differs from type 1. The genotype-phenotype correlation for cases with ristocetin cofactor activity (RCo)/antigen (Ag) ratios <0.60 is clear, whereas the von Willebrand factor (VWF):collagen binding (CB)/VWF:Ag ratio is normal in VWD 2M. Typical lab...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000214854

    authors: Hermans C,Batlle J

    更新日期:2009-01-01 00:00:00

  • Myelofibrosis and pancytopenia in systemic lupus erythematosus.

    abstract::A 13-year-old Saudi girl presented with severe clinical features of systemic lupus erythematosus of 3 months' duration. In addition to laboratory evidence of the disease, the patient was found to have pancytopenia and myelofibrosis. While pancytopenia was considerably improved by steroids, myelofibrosis was not revers...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000205641

    authors: el Mouzan MI,Ahmad MA,al Fadel Saleh M,al Sohaibani MO,al Gindan YM

    更新日期:1988-01-01 00:00:00

  • Clinical Management of Posterior Reversible Encephalopathy Syndrome after Allogeneic Hematopoietic Stem Cell Transplantation: A Case Series and Review of the Literature.

    abstract:BACKGROUND:Posterior reversible encephalopathy syndrome (PRES) is a rare but serious complication after allogeneic hematopoietic stem cell transplantation (alloHSCT). Among others, calcineurin inhibitors (CNI) for prophylaxis of graft-versus-host disease (GvHD) may promote the development of PRES, but the pathomechanis...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000430489

    authors: Schmidt V,Prell T,Treschl A,Klink A,Hochhaus A,Sayer HG

    更新日期:2016-01-01 00:00:00

  • Acute graft-versus-host disease resulting from normal donor blood transfusions.

    abstract::2 fatal cases of graft-versus-host disease (GvHD) occurred following blood product transfusions given to patients receiving standard chemotherapy for Hodgkin's disease. GvHD was established by HLA typing, clinical course, and compatible skin biopsy. 23 cases of GvHD following transfusion of blood products from normal ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206599

    authors: Burns LJ,Westberg MW,Burns CP,Klassen LW,Goeken NE,Ray TL,Macfarlane DE

    更新日期:1984-01-01 00:00:00

  • Platelet aggregation in diabetic retinopathy.

    abstract::Platelet aggregation in diabetic retinopathy was investigated in a group of 25 patients. An enhanced activity induced by epinephrine and arachidonic acid was found in this group as compared with the controls, whereas in adenosine diphosphate (ADP) platelet aggregation no differences were observed. Spontaneous aggregat...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207695

    authors: Creter D,Pavlotzky F,Savir H

    更新日期:1978-01-01 00:00:00