Therapeutic outcome of multifocal Langerhans cell histiocytosis in adults treated with the Special C regimen formulated by the Japan LCH Study Group

スポンサーリンク

概要

• 論文の詳細を見る
• 2013-01-01

著者

• Tojo Arinobu

  Department Of Cell Processing And Transfusion Institute Of Medical Science University Of Tokyo

• Kanegane Hirokazu

  Department Of Pediatrics Faculty Of Medicine Toyama Medical And Pharmaceutical University

• Wakita Hisashi

  Division Of Hematology And Oncology Japanese Red Cross Narita Hospital

• Morimoto Akira

  Department Of Pediatrics Graduate School Of Medical Science Kyoto Prefectural University Of Medicine

• Imamura Toshihiko

  Department Of Pediatrics Graduate School Of Medical Science Kyoto Prefectural University Of Medicine

• Shimazaki Chihiro

  Department Of Hematology Kyoto Social Insurance Hospital

• Kobayashi Yutaka

  Division Of Hematology And Oncology Department Of Internal Medicine Kyoto Second Red Cross Hospital

• Nishimura Ryosei

  Department Of Pediatrics Faculty Of Medicine Kanazawa University

• Imashuku Shinsaku

  Division Of Hematology Takasago-seibu Hospital

• Takahashi Satoshi

  Departmanets Of Immunology Graduate School Of Medical And Dental Sciences Niigata University

• IMAMURA Toshihiko

  Department of Pediatrics, Kyoto Prefectural University of Medicine

• YOSHIKAWA Kouhei

  Division of Hematology, Hikone Municipal Hospital

• TAKAHASHI Satoshi

  Department of Hematology/Oncology, Research Hospital, The Institute of Medical Science, The University of Tokyo

• TOJO Arinobu

  Department of Hematology/Oncology, Research Hospital, The Institute of Medical Science, The University of Tokyo

関連論文

• ブルトン・チロシン・キナーゼの第1イントロンにおける転写調節異常
• Early Ultrasonographic Diagnosis and Clinical Follow-up of Hepatic Veno-Occlusive Disease after Allogeneic Bone Marrow Transplantation in a Patient with Acute Lymphoblastic Leukemia
• Open Heart Operation in a Child With Congenital Heart Disease and Hereditary Spherocytosis
• Risk of Etoposide-Related Acute Myeloid Leukemia in the Treatment of Epstein-Barr Virus-Associated Hemophagocytic Lymphohistiocytosis
• Hepatocyte growth factor in transient myeloproliferative disorder of Down syndrome
• Distinct Clones Are Associated with the Development of Transient Myeloproliferative Disorder and Acute Megakaryocytic Leukemia in a Patient with Down Syndrome
• Mosaic Down syndrome-associated acute myeloid leukemia does not require high-dose cytarabine treatment for induction and consolidation therapy
• Bacterial Bloodstream Infection in Neutropenic Adult Patients after Myeloablative Cord Blood Transplantation : Experience of a Single Institution in Japan
• Pancreatic Hyperamylasemia and Hyperlipasemia in Association with Cytomegalovirus Infection following Unrelated Cord Blood Transplantation for Acute Myelogenous Leukemia
• Hemorrhagic Cystitis in Adults after Unrelated Cord Blood Transplantation : A Single-Institution Experience in Japan
• Varicella-Zoster Virus Encephalitis in a Patient Undergoing Unrelated Cord Blood Transplantation for Myelodysplastic Syndrome-Overt Leukemia
• Early-Onset Thyrotoxicosis after Unrelated Cord Blood Transplantation for Acute Myelogenous Leukemia
• Atypical Hypersensitivity to Mosquito Bites without Natural Killer Cell Proliferative Disease in an Adult Patient
• Unrelated Cord Blood Transplantation after Myeloablative Conditioning for Adult Patients with Refractory Anemia
• Human Herpesvirus 6 Variant B Infection in Adult Patients after Unrelated Cord Blood Transplantation
• Unrelated Cord Blood Transplantation with a Reduced-Intensity Conditioning Regimen following Autologous Transplantation for Multiple Myeloma
• Acute Myelogenous Leukemia M5b Developed during Clinical Remission of Castleman Disease
• Using Related Donors Other Than Genotypically HLA-Matched Siblings in Allogeneic Hematopoietic Stem Cell Transplantation for Hematologic Disease : A Single Institution Experience in Japan
• Second Allogeneic Hematopoietic Stem Cell Transplantation for Leukemia Relapse After First Allogeneic Transplantation : Outcome of 16 Patients in a Single Institution
• M-protein-positive chronic active Epstein-Barr virus infection: features mimicking HIV-1 infection
• Activation-dependent T cell expression of the X-linked lymphoproliferative disease gene product SLAM-associated protein and its assessment for patient detection
• Monosomies 7p and 12p and FLT3 internal tandem duplication : possible markers for diagnosis of T/myeloid biphenotypic acute leukemia and its clonal evolution
• Good Prognosis of Patients With Acute Promyelocytic Leukemia Who Achieved Second Complete Remission (CR) With a New Retinoid, Am80, After Relapse From CR Induced by All-trans-Retionic Acid
• Phase II and pharmacokinetic study of thalidomide in Japanese patients with relapsed/refractory multiple myeloma
• Clinical and Genetic Analyses of Presumed Shwachman-Diamond Syndrome in Japan
• Refractory Facial Cellulitis Following Cosmetic Rhinoplasty After Cord-blood Stem Cell Transplantation
• CD4/CD8 double-positive adult T cell leukemia with preceding cytomegaloviral gastroenterocolitis
• Establishment of novel cell lines derived form two patients with chronic myelogenous leukemia in blast crisis; IMS-BC1 and IMS-BC2 which exhibit markedly different sensitivity to apoptosis
• Toxicity and efficacy of ifosfamide, carboplatin and etoposide (modified ICE) as a salvage chemotherapy in Japanese patients with relapsed or refractory aggressive non-Hodgkin's lymphoma
• Recurrent Breast Cancer Treated Successfully with Mitomycin-C and Vinblastine after Failure of Both Doxorubicin-containing Regimen and Paclitaxel : A Case Report
• A Limited Sampling Model for Estimating Pharmacokinetics of CPT-11 and Its Metabolite SN-38
• Pharmacological Correlation between Total Drug Concentration and Lactones of CPT-11 and SN-38 in Patients Treated with CPT-11
• Cytogenetic Remissions Induced by Interferon α and Imatinib Mesylate are Immunologically Distinct in Chronic Myeloid Leukemia
• Three brothers of X-linked agammaglobulinemia : the relation between phenotype and neutropenia
• Peripheral blood lymphocyte subpopulations in three infants with hepatosplenomegaly caused by cytomegalovirus infection
• Mononucleosis-like illness in an infant associated with human herpesvirus 6 infection
• X-Linked Agammaglobulinemia Diagnosed in Adulthood : A Case Report
• X-Linked Lymphoproliferative Disease in an Adult
• Clinical features of adult acute leukemia with 11q23 abnormalities in Japan : a co-operative multicenter study
• Thrombotic thrombocytopenic purpura associated with myelodysplastic syndrome
• Dexamethasone Reduces the Risk of Bortezomib-Induced Pulmonary Complications in Japanese Myeloma Patients
• Langerhans cell histiocytosis with multifocal bone lesions : comparative clinical features between single and multi-systems
• Evans syndrome in a patient with Langerhans cell histiocytosis : possible pathogenesis of autoimmunity in LCH
• Autologous bone marrow transplantation for patients with advanced chronic myelogenous leukemia
• Early lineage switch in an infant acute lymphoblastic leukemia
• Pneumocystis jiroveci pneumonia as an atypical presentation of X-linked agammaglobulinemia
• Spontaneous regression of aleukemic leukemia cutis harboring a NPM/RARA fusion gene in an infant with cutaneous mastosytosis
• Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease
• Acute lymphoblastic leukemia after living donor liver transplantation
• Mutational Analysis of the WASP Gene in 2 Korean Families with Wiskott-Aldrich Syndrome
• Identification of mutations in the Bruton's tyrosine kinase gene, including a novel genomic rearrangements resulting in large deletion, in Korean X-linked agammaglobulinemia patients
• Outcome of pediatric patients with Langerhans cell histiocytosis treated with 2 chlorodeoxyadenosine : a nationwide survey in Japan
• A case of severe recurrent hepatitis with common variable immunodeficiency
• Biofeedback Training for Bronchial Asthma (Part I)
• A Trial of Biofeedback Treatment for Alopecia Areata
• Non-Hodgkin's Lymphoma of the Ascending Colon in a Patient with Becker Muscular Dystrophy : Report of a Case
• Mutations of syntaxin 11 and SNAP23 genes as causes of familial hemophagocytic lymphohistiocytosis were not found in Japanese people
• Control of hepatic veno-occlusive disease with an antithrombin-III concentrate-based therapy
• Prognostic Value of Early Response to Treatment Combined with Conventional Risk Factors in Pediatric Acute Lymphoblastic Leukemia
• Risk Factors for Cytomegalovirus Retinitis Following Bone Marrow Transplantation From Unrelated Donors in Patients With Severe Aplastic Anemia or Myelodysplasia
• Granulocytic Sarcoma Presenting with Severe Adenopathy (Cervical Lymph Nodes, Tonsils, and Adenoids) in a Child with Juvenile Myelomonocytic Leukemia and Successful Treatment with Allogeneic Bone Marrow Transplantation
• A Case of Budd-Chiari Syudrome Successfully Treated by Transcatheter Recanalixation of the Right Hepatic Vein and Transjugular Intrahepatic Portosystemic Shunt
• Comparison of mesenchymal stem cells derived from arterial, venous, and Wharton's jelly explants of human umbilical cord
• Hemophagocytic lymphohistiocytosis during maintenance treatment of precursor B-cell acute lymphoblastic leukemia
• A Novel Perforin Gene Mutation in a Japanese Family with Hemophagocytic Lymphohistiocytosis
• Characterization of a Novel Nonsense Mutation in the Interleukin-7 Receptor α Gene in a Korean Patient with Severe Combined Immunodeficiency
• Point mutation in intron 11 of Bruton's tyrosine kinase in atypical X-linked agammaglobulinemia
• Non-progressive viral myelitis in X-linked agammaglobulinemia
• identification of an SH2D1A Mutation in a Hypogammaglobulinemic Male Patient with a Diagnosis of Common Variable Immunodeficiency
• Infected urachal cyst ruptured during medical palliation
• Pharmacokinetic studies of intravenous glycosylated recombinant human granulocyte colony-stimulating factor in various hematological disorders: inverse correlation between the half-life and bone marrow myeloid cell pool
• Response to Imatinib Mesylate in a Patient with Idiopathic Hypereosinophilic Syndrome Associated with Cyclic Eosinophil Oscillations
• Hb Bristol-Alesha Presenting Thalassemia-Type Hyperunstable Hemoglobinopathy
• Hemophagocytic Syndrome Associated with Severe Adenoviral Pneumonia : Usefulness of Real-Time Polymerase Chain Reaction for Diagnosis
• Low Frequency of KIT Gene Mutation in Pediatric Acute Myeloid Leukemia with inv(16)(p13q22) : A Study of the Japanese Childhood AML Cooperative Study Group
• Factors predisposing to HTLV-1 infection in residents of the greater Tokyo area
• Dual antitumor mechanisms of Notch signaling inhibitor in a T-cell acute lymphoblastic leukemia xenograft model
• A novel immunoregulatory protein in human colostrum, syntenin-1, for promoting the development of IgA-producing cells from cord blood B cells
• Bortezomib plus dexamethasone for relapsed or treatment refractory multiple myeloma : the collaborative study at six institutes in Kyoto and Osaka
• Association analysis of the NOD2 gene with susceptibility to graft-versus-host disease in a Japanese population
• Autoimmune lymphoproliferative syndrome mimicking chronic active Epstein-Barr virus infection
• Atypical case of X-linked agammaglobulinemia diagnosed at 45 years of age
• Mislocalization or low expression of mutated Shwachman-Bodian-Diamond syndrome protein
• Six-year-old girl with primary cutaneous aggressive epidermotropic CD8^+ T-cell lymphoma
• Hematopoietic stem cell transplantation with reduced intensity conditioning from a family haploidentical donor in an infant with familial hemophagocytic lymphohistocytosis
• Treatment of patients with hypothalamic-pituitary lesions as adult-onset Langerhans cell histiocytosis
• Analysis of 43 cases of Langerhans cell histiocytosis (LCH)-induced central diabetes insipidus registered in the JLSG-96 and JLSG-02 studies in Japan
• Monosomy 13 in metaphase spreads is a predictor of poor long-term outcome after bortezomib plus dexamethasone treatment for relapsed/refractory multiple myeloma
• Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes
• Delayed onset adenosine deaminase deficiency associated with acute disseminated encephalomyelitis
• Another promising treatment option for neuroblastoma-associated opsoclonus-myoclonus syndrome by oral high-dose dexamethasone pulse : Lymphocyte markers as disease activity
• Two Siblings Diagnosed to Have Transthyretin-related Familial Amyloid Cardiomyopathy Around the Same Time at Different Hospitals
• Rapidly Progressing Fatal Adult Multi-Organ Langerhans Cell Histiocytosis Complicated with Fatty Liver Disease
• The Response to Second-line Induction with Bortezomib and Dexamethasone is Predictive of Long-term Outcomes Prior to High-dose Chemotherapy with Autologous Stem Cell Transplantation for Multiple Myeloma
• Serial measurement of free light chain detects poor response to therapy early in three patients with multiple myeloma who have measurable M-proteins
• Central Nervous System Leukemia on Magnetic Resonance Imaging
• Fatal Acute Tumor Lysis Syndrome following Intrathecal Chemotherapy for Acute Lymphoblastic Leukemia with Meningeal Involvement
• Relapsing Campylobacter Coli Bacteremia with Reactive Arthritis in a Patient with X-linked Agammaglobulinemia
• Therapeutic outcome of multifocal Langerhans cell histiocytosis in adults treated with the Special C regimen formulated by the Japan LCH Study Group
• Harmonization of molecular monitoring of chronic myeloid leukemia therapy in Japan

もっと見る 閉じる

スポンサーリンク