Amylase-producing Bence Jones multiple myeloma with pancreatitis-like symptoms.

Abstract:

:Amylase-producing tumors are mainly adenocarcinomas and, in rare instances, multiple myelomas. We describe here a first case of amylase-producing Bence Jones type myeloma with pancreatitis-like symptoms and the second in a Caucasian patient. The finding of salivary-type hyperamylasemia in a 72-year-old female with a possible pancreatitis made us suspect the diagnosis. Amylase production was observed in bone marrow cultures in which 96% of cellularity was composed of plasmablasts. Serum amylase level decreased when chemotherapy was given.

journal_name

Acta Haematol

journal_title

Acta haematologica

authors

Lopez J,Ulibarrena C,Gonzalez-Porque P,Navas G,Roldan E,Cancelas JA,Perez-Oteyza J,Burgaleta C,García-Laraña J,Sastre JL

doi

10.1159/000204384

subject

Has Abstract,Author List Incomplete

pub_date

1993-01-01 00:00:00

pages

99-101

issue

2

eissn

0001-5792

issn

1421-9662

journal_volume

90

pub_type

杂志文章
  • Agranulocytosis in a patient with thalassaemia major during treatment with the oral iron chelator, 1,2-dimethyl-3-hydroxypyrid-4-one.

    abstract::Agranulocytosis developed in a 20-year-old Greek patient with beta-thalassaemia major, 11 weeks after commencing chelation with the oral iron chelator 1,2-dimethyl-3-hydroxypyrid-4-one (L1) and 6 weeks after receiving the drug at a total daily dose of 105 mg/kg. The patient presented with generalised weakness, low-gra...

    journal_title:Acta haematologica

    pub_type: 临床试验,杂志文章

    doi:10.1159/000204494

    authors: al-Refaie FN,Veys PA,Wilkes S,Wonke B,Hoffbrand AV

    更新日期:1993-01-01 00:00:00

  • Lymphocytotoxic activity of monoclonal immunoglobulins in plasmalymphocytic diseases.

    abstract::95 of 1,019 (9.3%) sera with monoclonal immunoglobulins (MIg) were found to have cold-reacting lymphocytotoxins (LCT). There was no difference in the prevalence of LCT in multiple myeloma, macroglobulinemia, cancer, lymphoma or benign monoclonal gammopathy. Prevalence of LCT was similar in various classes and types of...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206328

    authors: Pruzanski W,Capes H,Ramirez G,Falk J

    更新日期:1985-01-01 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

  • Factor X inhibitor: a fulminant presentation and fatal course of a rare syndrome in a 59-year-old male.

    abstract::Factor X inhibitors are rare. The few cases documented in the literature have occurred after viral prodromes, in association with cancer, or after exposure to antibiotics. Acquired factor X deficiencies are also rare and their etiology is largely unknown. We report a new case of a factor X inhibitor and review prior c...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000342115

    authors: Gollard R,Rahman S,Ratnasabapathy R

    更新日期:2013-01-01 00:00:00

  • Human urinary erythropoietin: preparation with high potency.

    abstract::Human urinary erythropoietin has been purified to homogeneity. The seven-step procedure yielded a preparation with a potency of 225,000 U/mg protein. SDS-polyacrylamide gel electrophoretic analysis of the purified hormone revealed a single protein band with a molecular weight of about 35,000 that migrated with the bio...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000205057

    authors: Matsushita J,Kawakita M,Shibuya K,Koishihara Y,Sakaguchi M,Takatsuki A

    更新日期:1990-01-01 00:00:00

  • Scanning immunoelectron microscopy of hairy cell leukemia.

    abstract::Scanning electron microscopy has shown a typical cell surface morphology in hairy cell leukemia. Scanning immunoelectron microscope techniques, utilizing monoclonal antibodies and colloidal gold particles, have recently become available. Eight patients with hairy cell leukemia have been studied with a panel of monoclo...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206218

    authors: Soligo D,Lambertenghi-Deliliers G,Nava MT,Polli N,Cattoretti G,Polli EE

    更新日期:1985-01-01 00:00:00

  • Eosinophilic gastroenteritis or eosinophilic chloroma?

    abstract::Granulocytic sarcoma of the small intestine preceding or as the presenting feature of acute myelogenous leukemia with chromosome 16 abnormalities has been observed in at least 4 patients. We report the case of a patient initially diagnosed with eosinophilic gastroenteritis, responding to corticosteroid treatment for 2...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000079729

    authors: Julia A,Nomdedeu JF

    更新日期:2004-01-01 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

  • Red cell metabolism and severe neonatal jaundice in West Malaysia.

    abstract::A study was carried out of 332 babies suffering from severe neonatal jaundice who were admitted to the General Hospital, Kuala Lumpar, Malaysia. Of the 332 neonates, 51 were premature and 281 were full-term babies, 178 (110 Chinese, 58 Malay, 9 Indian and 1 European-Pakistani) had bilirubin levels of 20 mg% or higher,...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207822

    authors: Lie-Injo LE,Virik HK,Lim PW,Lie AK,Ganesan J

    更新日期:1977-01-01 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

  • Marker chromosome in myeloproliferative syndrome.

    abstract::Chromosomal aberrations in a case of atypic myeloproliferative syndrome are reported. The analysis was carried out on short-term cultures of sternal bone marrow with the ASG and fluorescence method. 90% of the metaphases studied showed pseudoliploidy: one of the chromosomes 12 was missing and one submedian marker chro...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000208052

    authors: Fleischmann T,Krizsa F

    更新日期:1975-01-01 00:00:00

  • Immunological profile after splenectomy in children with beta-thalassaemia major.

    abstract::The in vitro immune functions of peripheral blood lymphocytes have been studied in 12 children with beta-thalassaemia major and hypersplenism. The study was performed prior to splenectomy and on the 2nd, 6th, 15th and 30th day after splenectomy. It was found that before splenectomy, patients had low numbers of blood l...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000205886

    authors: Mandalenaki-Lambrou K,Vrachnou E,Calogeropoulou C,Ladis V,Kattamis C

    更新日期:1987-01-01 00:00:00

  • Electron microscope and high resolution autoradiographic studies of megaloblastic erythropoiesis.

    abstract::Bone marrow fragments from 10 patients with a megaloblastic anaemia due to vitamin B12 or folate deficiency were studied by electron microscopy and electron microscope autoradiography. A proportion of the erythroblasts showed ultrastructural abnormalities. Some of the cells containing autophagic vacuoles, large sidero...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207854

    authors: Wickramasinghe SN,Bush V

    更新日期:1977-01-01 00:00:00

  • A fourth case of 8p11 myeloproliferative disorder transforming to B-lineage acute lymphoblastic leukaemia. A case report.

    abstract::A 56-year-old male presented with inguinal lymphadenopathy and leucocytosis (WBC 98 x 10(9)/l). Bone marrow morphology showed myeloid hyperplasia, with eosinophilia. Cytogenetic analysis showed no evidence of the Philadelphia chromosome, and fluorescence in situ hybridisation studies for the BCR/ABL fusion were negati...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000046638

    authors: JabbarAl-Obaidi M,Rymes N,White P,Pomfret M,Smith H,Starczynski J,Johnson R

    更新日期:2002-01-01 00:00:00

  • Plasma cortisol in sickle cell disease.

    abstract::The plasma cortisol levels of 108 children aged 1-16 years with various Hb genotypes (AA, AS and SS) were measured. The mean plasma cortisol levels of both the AS and SS groups (during steady state) fell within the normal range but the mean of the SS group is significantly lower than the AA group. In fact, 9 of the si...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000205689

    authors: Osifo BO,Lukanmbi FA,Adekile A

    更新日期:1988-01-01 00:00:00

  • The delta-globin RNA transcript level in beta-thalassemia carriers.

    abstract::Increased levels of hemoglobin A(2) (HbA(2)) are present in most beta-thalassemia carriers. The mechanism of this effect is not understood, although the increase may result from transcriptional and posttranscriptional changes. In the present study, we quantitate delta-globin mRNA levels in peripheral-blood-enriched re...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000040959

    authors: Huang SZ,Zeng FY,Chen MJ,Ren ZR,Shen M,Rodgers GP,Schechter AN,Zeng YT

    更新日期:1999-01-01 00:00:00

  • Micromegakaryocytes in Human Bone Marrow.

    abstract::Micromegakaryocytes (MMK) were defined morphologically by the cell area, nucleus form and cytoplasmic structure. Bone marrow smears of 7,156 patients were retrospectively analyzed. MMK were found most frequently and abundantly in acute non-lymphatic leukaemia, chronic myeloid leukaemia and pre-leukaemia. The presence ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207213

    authors: Wiesneth M,Pflieger H,Kubanek B,Heimpel H

    更新日期:1980-01-01 00:00:00

  • Chronic Pain Does Not Impact Baseline Circulating Cytokine Levels in Adults with Sickle Cell Disease.

    abstract::Chronic pain affects 50% of adults with sickle cell disease (SCD). Although inflammation is thought to contribute to the pathogenesis of chronic pain, no studies have examined the differences in circulating cytokines between patients with SCD with and without chronic pain. We performed an observational cohort study us...

    journal_title:Acta haematologica

    pub_type: 新闻

    doi:10.1159/000507563

    authors: Karafin MS,Simpson P,Field JJ

    更新日期:2021-01-01 00:00:00

  • Autologous marrow reconstitutions in severe aplastic anaemia after ALG pretreatment and HL-A semi-incompatible bone marrow cell transfusion.

    abstract::Three consecutive patients considered to have end-stage acquired aplastic anaemia were given 100-160 mg/kg antilymphocyte globulin (ALG) i.v. followed by an infusion of 2-3.8 x 10(8) nucleated marrow cells/kg i.v. from HL-A one haplotype-identical, MLC-positive family donors. All patients showed autologous marrow reco...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000208005

    authors: Jeannet M,Speck B,Rubinstein A,Pelet B,Wyss M,Kummer H

    更新日期:1976-01-01 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

  • Serum levels of G-CSF, IL-3, IL-6 and GM-CSF after a single intraperitoneal dose of rhG-CSF in lethally irradiated B6D2F1 mice.

    abstract::The objective of this study was to assess the pharmacokinetics of rhG-CSF after a single intraperitoneal injection 2 h post-TBI in B6D2F1 lethally irradiated mice and to analyze the effect of rhG-CSF on the endogenous response of interleukin-3 (IL-3), interleukin-6 (IL-6) and granulocyte-macrophage colony-stimulating ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000203604

    authors: Kádár E,Sureda A,Mangues MA,Inglés-Esteve J,Valls A,García J

    更新日期:1997-01-01 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

  • Immunological analysis of acquired factor VIII inhibitor in a case with immunologic disorder.

    abstract::Coagulation factor VIII inhibitor arising in a patient with autoimmune disease was immunologically analyzed. A 63-year-old man who had been diagnosed as suffering from polyarteritis nodosa was treated with prednisolone for 10 years. Severe bleeding tendency developed and coagulation studies demonstrated a high titer o...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000204879

    authors: Okamura T,Yamauchi Y,Fukuda T,Suehiro K,Murakawa M,Shibuya T,Nagasawa K,Harada M,Niho Y

    更新日期:1991-01-01 00:00:00

  • Lymphoproliferative disorders after immunosuppressive therapy for aplastic anemia: a case report and literature review.

    abstract::A 61-year-old Japanese man was referred to our hospital in 2002 due to severe pancytopenia. Bone marrow and peripheral blood findings indicated he had severe aplastic anemia (AA). A whole-body CT scan and Ga scintigraphy revealed no abnormal findings. Antithymocyte globulin and cyclosporine A (CyA) were administered a...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000209225

    authors: Suzuki Y,Niitsu N,Hayama M,Katayama T,Ishii R,Osaka M,Miyazaki K,Danbara M,Horie R,Yoshida T,Nakamura N,Higashihara M

    更新日期:2009-01-01 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

  • Bacteria in blood smears: overwhelming sepsis or trivial contamination.

    abstract::It is unusual to find microorganisms in peripheral blood smears, and their presence is frequently associated with overwhelming sepsis and consequently a poor prognosis. In this report, we demonstrate 4 cases with bacteria in blood smears. Two of them had a fatal outcome, but the other 2 were caused by a contamination ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000058318

    authors: van der Meer W,Verwiel JM,Gidding CE,de Metz M,de Keijzer MH

    更新日期:2002-01-01 00:00:00

  • Biochemical approach to bovine leukemia.

    abstract::Many bovine leukemic lymphocytes produce virus particles when kept in survival cultures in Eagle's Minimum Essential Medium supplemented with 20 percent of inactivated fetal calf serum. Virus particles equilibrate at a density of 1.16 g/ml in sucrose gradients and at a density of 1.12 g/ml in metrizamide gradients. Si...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000208076

    authors: Kettmann R,Mammerickx M,Dekegel D,Ghysdael J,Portetelle D,Burny A

    更新日期:1975-01-01 00:00:00

  • Continuous complete hematological and cytogenetic remission with molecular minimal residual disease 9 years after discontinuation of interferon-alpha in a patient with Philadelphia chromosome-positive chronic myeloid leukemia.

    abstract::Interferon-alpha has been used as standard therapy for patients with Philadelphia-positive chronic myeloid leukemia (CML) for more than 20 years. Recently randomized trials have shown a superiority of the tyrosine kinase inhibitor imatinib in respect to its efficacy to induce complete hematological and cytogenetic rem...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000089476

    authors: Verbeek W,König H,Boehm J,Kohl D,Lange C,Heuer T,Scheibenbogen C,Reis HE,Hochhaus A,Graeven U

    更新日期:2006-01-01 00:00:00

  • Circulating platelet aggregates and thrombocytopenia induced by intravenous infusions of arachidonic and lauric acids in guinea pigs.

    abstract::Slow intravenous infusion of Na laurate (NaL) into guinea pigs caused a rapid appearance of platelet aggregates in the arterial blood and a precipitous fall in platelet counts. During the infusion of Na arachidonate (NaA) thrombocytopenia developed slowly, and few and smaller platelet aggregates appeared in the arteri...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207864

    authors: Rafflenbeul D,Zbinden G

    更新日期:1977-01-01 00:00:00

  • Can Biomarkers of Coagulation, Platelet Activation, and Inflammation Predict Venous Thromboembolism in Patients with Haematological Malignancies?

    abstract:BACKGROUND:The incidence of venous thromboembolism (VTE) in haematological malignancies varies according to the type and grade of the disease and clinical variables, and there is a need to develop a tool to predict the occurrence of VTE in cancer patients at diagnosis to tailor prophylactic anticoagulation use during t...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000496914

    authors: Elmoamly S,Mattar M,Yacoub MF,Afif A

    更新日期:2019-01-01 00:00:00