Antithrombin III during high-dose cytosine arabinoside therapy with or without asparaginase.

Abstract:

:Fourteen patients with hematologic neoplasia (11 acute myeloid leukemias, 2 non-Hodgkin's lymphomas and 1 blast crisis of chronic myeloid leukemia) who underwent high-dose cytosine arabinoside (HIDARAC) therapy with or without sequential asparaginase (ASNase) were investigated in order to evaluate liver toxicity and a possible decrease in antithrombin III (AT III) plasma level. AT III was found decreased only in patients who received ASNase, whereas HIDARAC alone did not influence AT III levels. It is pointed out that a single dose of ASNase seems to be sufficient to induce a decrease in AT III. A mild and transient liver toxicity due to HIDARAC therapy does not seem to be of any clinical relevance.

journal_name

Acta Haematol

journal_title

Acta haematologica

authors

Marra R,Pagano L,De Stefano V,Leone G,Bizzi B

doi

10.1159/000206094

subject

Has Abstract

pub_date

1986-01-01 00:00:00

pages

96-9

issue

2

eissn

0001-5792

issn

1421-9662

journal_volume

75

pub_type

临床试验,杂志文章
  • Pyrimidine 5'-nucleotidase acquired deficiency in beta-thalassemia: involvement of enzyme-SH groups in the inactivation process.

    abstract::Pyrimidine 5'-nucleotidase (P5'N) partial deficiency has been described in several hematological disorders and also in the beta-thalassemic trait. To check if the P5'N deficiency in thalassemia was acquired we used thalassemic red cells (from either homo- or heterozygous subjects), whose P5'N activity was lower than i...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000205286

    authors: David O,Vota MG,Piga A,Ramenghi U,Bosia A,Pescarmona GP

    更新日期:1989-01-01 00:00:00

  • A case of pure red cell aplasia complicated with diffuse large B cell lymphoma, T-cell-rich/histiocyte-rich variant: effectiveness of rituximab and implications for a common immunopathogenic role of B lymphocytes.

    abstract::Diffuse large B cell lymphoma, T-cell-rich/histiocyte-rich variant (DLBL-TH), is characterized by the presence of neoplastic B cells set in a background containing numerous non-neoplastic T lymphocytes and histiocytes. We report here the case of a patient with DLBL-TH who developed overt pure red cell aplasia (PRCA) f...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000084450

    authors: Oyaizu N,Kozai Y,Kodo H,Sunaga S,Iwabuchi K,Higashihara M,Mori S

    更新日期:2005-01-01 00:00:00

  • Bernard-Soulier syndrome: diagnosis by an ELISA method using monoclonal antibodies in 2 new unrelated patients.

    abstract::Two unrelated patients with Bernard-Soulier syndrome and their relatives were studied. The patients demonstrated severe bleeding diathesis, the relatives were asymptomatic. The propositi showed the characteristic abnormalities of the syndrome: thrombocytopenia, a percentage of giant platelets higher than 65%, prolonge...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206125

    authors: De Marco L,Fabris F,Casonato A,Fabris P,Dal Ben MG,Barbato A,Girolami A

    更新日期:1986-01-01 00:00:00

  • 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

  • Inherited bleeding syndromes in Jordan.

    abstract::This paper presents data on the occurrence and pattern of inherited bleeding syndromes (IBS) in Jordan, a hitherto unexplored problem. In 1978, during the first 12 months of a prospective study at a major medical center, 91 patients from 51 families were diagnosed as having IBS. All patients were referred because of m...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207625

    authors: Alsabti EA,Hammadi M

    更新日期:1979-01-01 00:00:00

  • Serum ferritin levels in thalassemias and the effect of splenectomy.

    abstract::Iron overload is a constant and the more important complication in thalassemia. Serum ferritin concentration accurately reflects body iron stores. A total of 245 thalassemic patients aged 12-55 years were examined, 71 having Hb H disease and 174 beta-thalassemia/Hb E disease. The patients received minimal or no blood ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207129

    authors: Pootrakul P,Vongsmasa V,La-ongpanich P,Wasi P

    更新日期:1981-01-01 00:00:00

  • Clones with 3 Ph1 and 4 Ph1 in the terminal phase of three cases of chronic myeloid leukemia.

    abstract::G-banded cytogenetic studies of 3 male patients in the terminal phase of chronic myeloid leukemia showed the following abnormalities: in the first case, the presence of a medullar cell line with 51 chromosomes and 3 Ph1; in the second case, a clone with 65 chromosomes and 4 Ph1, and in the third patient a clone with 5...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207047

    authors: Cabrol C,Peytremann R,Maurice PA

    更新日期:1982-01-01 00:00:00

  • Natural killer cell activity and T subpopulations in thalassemia major.

    abstract::Natural killer (NK) cell activity against K562 cell targets and the distribution of T cell subpopulations were investigated in the peripheral blood of 25 patients affected by beta thalassemia major, 18 clinically healthy heterozygotes, and 25 age-matched normal subjects. It was found that thalassemia major patients di...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206598

    authors: Neri A,Brugiatelli M,Iacopino P,Callea V,Ronco F

    更新日期:1984-01-01 00:00:00

  • Serum folate binding capacity in leukemias, liver diseases and pregnancy.

    abstract::Total and unsaturated folate binding capacity (TFBC, UFBC) have been measured in sera of selective groups of patients to study the role of cell turnover, cell necrosis and the effect of pregnancy in determining their concentrations in blood. The mean value of TFBC in 35 normal sera was 151 +/- (SD) 53 pg/ml with a sat...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207657

    authors: Corrocher R,Bambara LM,Pachor ML,Biasi D,Stanzial A,De Sandre G

    更新日期:1979-01-01 00:00:00

  • Immunoglobulin therapy for autoimmune neutropenia in Hodgkin's disease.

    abstract::We describe a patient with recurrence of Hodgkin's disease and severe liver disease of unknown origin in whom autoimmune neutropenia developed. Because of possible seronegative viral hepatitis he was treated with high-dose intravenous immunoglobulin instead of steroids. He responded with a prompt but transitory increa...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000203968

    authors: Schoengen A,Fembacher PM,Schulz PC

    更新日期:1995-01-01 00:00:00

  • Changes in peripheral blood mononuclear cell subpopulations during antithymocyte globulin therapy for severe aplastic anemia.

    abstract::The short-term effect of a domestically produced equine antithymocyte globulin (ATG) was analyzed in 6 patients with acquired severe aplastic anemia (AA). All patients received 5 doses of ATG every other day in a 60-min intravenous infusion. Five peripheral blood immunoregulatory mononuclear cell (MNC) subsets, define...

    journal_title:Acta haematologica

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1159/000205557

    authors: López-Karpovitch X,Zarzosa ME,Cárdenas MR,Piedras J

    更新日期:1989-01-01 00:00:00

  • Apoptosis in relation to CD34 antigen expression in normal and myelodysplastic bone marrow.

    abstract::An increased bone marrow (BM) apoptosis is one of the mechanisms responsible for the ineffective hematopoiesis of myelodysplastic syndromes (MDS). It is controversial whether the excessive apoptosis in myelodysplasia predominantly involves the subset of progenitor cells or of maturing cells. We investigated the degree...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000067275

    authors: Pecci A,Travaglino E,Klersy C,Invernizzi R

    更新日期:2003-01-01 00:00:00

  • Sideroblast score: A sensitive indicator of iron deficiency and hypoproliferative anemia.

    abstract::The detection and enumeration of sideroblasts depend critically on the method used for iron staining of bone marrow smears. Several methods proposed for semiquantitative evaluation of bone marrow hemosiderin (iron stores) were compared with respect to their suitability for detection of normal and abnormal sideroblasts...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207856

    authors: Baumgartner-Stäubli R,Beck EA

    更新日期:1977-01-01 00:00:00

  • Evidence for an erythropoietin-stimulating factor in patients with renal and hepatic disease.

    abstract::Recently, a factor was discovered in the serum of hepatectomized animals which was capable of augmenting the hepatic erythropoietin response to hypoxia when injected into normal rats. This substance was localized in the liver via an in situ perfusion technique and was termed the hepatic erythropoietic factor (HEF). Pa...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206884

    authors: Naughton BA,Liu P,Naughton GK,Gordon AS

    更新日期:1983-01-01 00:00:00

  • Molecular findings and classification of malignant lymphomas.

    abstract::We review the problem of lymphoma classification in the light of the Revised European-American Lymphoma (REAL) scheme, recently proposed by the International Lymphoma Study Group (ILSG). The REAL classification is a list of clinicopathologic entities, all well known from the literature, upon which the ILSG members agr...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000203875

    authors: Pileri SA,Ceccarelli C,Sabattini E,Santini D,Leone O,Damiani S,Leoncini L,Falini B

    更新日期:1996-01-01 00:00:00

  • Concomitant Primary Hyperparathyroidism in Patients with Multiple Myeloma: A Possible Link?

    abstract::Hypercalcemia is a significant feature of patients with active multiple myeloma (MM) with extensive bone disease. Among the causes of non-neoplastic hypercalcemia, primary hyperparathyroidism (PHPT) is one of the most common, leading to osteoporosis and bone fractures. Interestingly, some preclinical data indicate tha...

    journal_title:Acta haematologica

    pub_type:

    doi:10.1159/000509768

    authors: Notarfranchi L,Marchica V,Dalla Palma B,Pelagatti L,Burroughs-Garcia J,Pedrazzoni M,Ruffini L,Cetani F,Marcocci C,Giuliani N

    更新日期:2020-09-09 00:00:00

  • CD56-positive acute lymphoblastic leukemia.

    abstract::We report a patient with lung cancer who developed CD56-positive acute lymphoblastic leukemia. He was referred to our hospital for thrombocytopenia. Atypical cells were found in the blood and the bone marrow. These cells were immunophenotypically positive for CD3epsilon, CD56, and terminal deoxynucleotidyl transferase...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000087891

    authors: Matano S,Terahata S,Nakamura S,Kobayashi K,Sugimoto T

    更新日期:2005-01-01 00:00:00

  • A drug-induced haemolytic anaemia due to Hb Torino (alpha43(CD1)Phe replaced by Val). second finding in an Italian family.

    abstract::The unstable haemoglobin, Tb Torino (alpha43(CD1)Phe replaced by Val), has been found for the second time in a family from the Treviso region of Italy. The haemoglobin has a slightly lower oxygen affinity than normal. In both cases, the abnormal haemoglobin is associated with inclusion body anaemia but the course of t...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207942

    authors: Sansone G,Sciarratta GV,Lang A,Lorkin PA,Lehmann H

    更新日期:1976-01-01 00:00:00

  • Glucose-6-phosphate dehydrogenase Velletri.

    abstract::A new variant of red cell glucose-6-phosphate dehydrogenase (G6PD) has been found in a Caucasian man with congenital non-spherocytic haemolytic anaemia. This variant has reduced activity, increased thermolability, increased Michaelis constants for glucose-6-phosphate and NADP, slightly increased electrophoretic mobili...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207869

    authors: Mandelli F,Amadori S,De Laurenzi A,Kahn A,Isacchi G,Papa G

    更新日期:1977-01-01 00:00:00

  • High incidence of conservative RAS mutations in acute myeloid leukemia.

    abstract::RAS mutations are found in about 25% of acute myeloid leukemia (AML) cases. The importance of these changes is unknown. If RAS mutations confer growth advantage to leukemia subclones in which they emerge, substantially more nonconservative than conservative mutations should be found. The incidence of conservative muta...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000204200

    authors: Aurer I,Labar B,Nemet D,Ajduković R,Bogdanić V,Gale RP

    更新日期:1994-01-01 00:00:00

  • Peculiar Congenital Factor VII Defect with the Proposita and Her Mother Showing the Same Compound Heterozygosity for Thr384Met and Arg413Gln.

    abstract:OBJECTIVE:To investigate a family with factor VII (FVII) deficiency from Argentina. PATIENTS AND METHODS:The proposita is a 14-year-old girl who presented with a mild to moderate bleeding tendency. Menorrhagia is controlled with periodical administration of small doses of recombinant FVII concentrate. The mother of th...

    journal_title:Acta haematologica

    pub_type:

    doi:10.1159/000507071

    authors: Girolami A,Paoletti M,Ferrari S,Garcia D

    更新日期:2021-01-01 00:00:00

  • Relationship of lymphocyte anisocytosis in chronic lymphatic leukaemia to mouse red cell rosetting capacity and clinical stage.

    abstract::In 34 patients with chronic lymphatic leukaemia (CLL) the lymphocytes have been separated and sized using a C1000 Channelyzer. The modal volume and the volume range of the populations have been obtained and related to clinical stage and mouse red blood cell (MRBC) rosetting capacity. Over 1 year's observation with sev...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206714

    authors: Wastell HJ,Proctor SJ

    更新日期:1983-01-01 00:00:00

  • A new method for the detection of the plasminogen activator content of vein walls.

    abstract::The plasminogen activator content of a vein wall has been measured by estimating the radio-activity released from a 125I-tagged fibrin clot by incubating that clot with a known weight of the vein wall. This method could be used in the investigation of the fibrinolytic system of the body in its normal distribution and ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207720

    authors: Johnson RH,Mansfield AO

    更新日期:1978-01-01 00:00:00

  • A severe case of cefoxitin-induced immune hemolytic anemia.

    abstract::Drug-induced immune hemolytic anemia is a rare but underdiagnosed and potentially fatal condition. We report a case of severe hemolytic anemia induced by cefoxitin in a 45-year-old woman admitted with menometrorrhagia. Hemoglobin levels reached a nadir of 4.7 g/dl approximately 72 h after cefoxitin initiation, and hem...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000320169

    authors: Leaf DE,Langer NB,Markowski M,Garratty G,Diuguid DL

    更新日期:2010-01-01 00:00:00

  • Methylprednisolone in advanced chronic lymphocytic leukaemia: rationale for, and effectiveness of treatment suggested by DiSC assay.

    abstract::The effect of methylprednisolone on fresh cells from patients with chronic lymphocytic leukaemia (CLL) has been studied using the differential staining cytotoxicity (DiSC) assay resulting in LC90s of < or = 0.2 to 2,000 micrograms/ml. Cells from previously treated patients were, on average, significantly more sensitiv...

    journal_title:Acta haematologica

    pub_type: 临床试验,杂志文章

    doi:10.1159/000204115

    authors: Bosanquet AG,McCann SR,Crotty GM,Mills MJ,Catovsky D

    更新日期:1995-01-01 00:00:00

  • Mesenchymal stromal cells as an adjuvant treatment for severe late-onset hemorrhagic cystitis after allogeneic hematopoietic stem cell transplantation.

    abstract::The management of severe late-onset hemorrhagic cystitis (LO-HC) after allogeneic hematopoietic stem cell transplantation (HSCT) is still challenging. Because mesenchymal stromal cells (MSCs) possess anti-inflammatory and tissue repair-promoting properties, we retrospectively analyzed the efficacy and safety of MSC in...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000362530

    authors: Wang Y,Chen F,Gu B,Chen G,Chang H,Wu D

    更新日期:2015-01-01 00:00:00

  • Acquired pure red-cell aplasia associated with an increase of T cells bearing receptors for the Fc of IgG.

    abstract::A case of steroid-resistant acquired pure red-cell aplasia associated with a relative and absolute increase of TG cells is described. Removal of T cells enhanced erythroid colony and burst formation in vitro, and it is suggested that TG cells may be implicated in the pathogenesis of this case of acquired pure red-cell...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207191

    authors: Linch DC,Cawley JC,MacDonald SM,Masters G,Roberts BE,Antonis AH,Waters AK,Sieff C,Lydyard PM

    更新日期:1981-01-01 00:00:00

  • Effect of granulocyte/colony-stimulating factor on the onset of the adult respiratory distress syndrome.

    abstract::To evaluate the effect of granulocyte/colony-stimulating factor (G-CSF) on the onset of the adult respiratory distress syndrome (ARDS), we investigated whether the incidence of ARDS due to pulmonary infection differed between the G-CSF group which received chemotherapy with G-CSF and historical controls without G-CSF....

    journal_title:Acta haematologica

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1159/000040937

    authors: Takahashi Y,Kobayashi Y,Chikayama S,Ikeda M,Kondo M

    更新日期:1999-01-01 00:00:00

  • Fetal liver transplantation in aplastic anemia.

    abstract::Fetal liver transplantation was attempted in 7 patients with aplastic anemia. 4 of these patients showed a partial response as evidenced by decrease in blood transfusion requirements and increase in the peripheral blood counts and hematopoietic cells in the bone marrow. Bone marrow culture studies revealed evidence of...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207558

    authors: Kansal V,Sood SK,Batra AK,Adhar G,Malviya AK,Kucheria K,Balakrishnan K

    更新日期:1979-01-01 00:00:00

  • The relationship between the blood and vein wall fibrinolytic activities in response to surgical trauma.

    abstract::The fibrinolytic response to surgical trauma was studied longitudinally in 7 pigs by measuring the fibrinolytic activity in the blood and vein wall simultaneously. The results indicated a marked suppression in fibrinolytic activity in the blood which was closely correlated with the activity in the vein wall. This corr...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207397

    authors: Wu AV,Mansfield AO

    更新日期:1980-01-01 00:00:00