Oxford Handbook of Clinical Haematology
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Oxford Handbook of Clinical Haematology

Oxford Medicine Online
 

Symbols and abbreviations

  • Formula
    cross-reference

  • decreased

  • increased
  • Formula
    important
  • Formula
    very important

  • normal
  • Formula
    websites

  • female

  • male

  • primary

  • secondary
  • 2,3 DPG
    2,3 diphosphoglycerate
  • 2-CDA
    2-chlorodeoxyadenosine
  • A2-M
    alpha2 microglobulin
  • 6-MP
    6-mercaptopurine
  • 99mTc-MIBI
    99mTc methoxyisobutyl-isonitride or 99mTc-MIBI scintigraphy
  • AA
    aplastic anaemia or reactive amyloidosis
  • Ab
    antibody
  • ABVD
    adriamycin (doxorubicin), bleomycin, vinblastine,
  • ACD
    acid-citrate-dextrose or anaemia of chronic disease
  • ACE
    angiotensin converting enzyme
  • ACL
    anticardiolipin antibody
  • ACML
    atypical chronic myeloid leukaemia
  • ADA
    adenosine deaminase
  • ADE
    cytosine arabinoside (Ara-C) daunorubicin etoposide
  • ADP
    adenosine 5-diphosphate
  • AFB
    acid fast bacilli
  • Ag
    antigen
  • AIDS
    acquired immunodeficiency syndrome
  • AIHA
    autoimmune haemolytic anaemia
  • AIN
    autoimmune neutropenia
  • AITL
    angio-immunoblastic T-cell lymphoma
  • AL
    (1°) amyloidosis
  • ALB
    serum albumin
  • ALCL
    anaplastic large cell lymphoma
  • ALG
    anti-lymphocyte globulin
  • ALIPs
    abnormal localization of immature myeloid precursors
  • ALL
    acute lymphoblastic leukaemia
  • ALS
    advanced life support
  • ALT
    alanine aminotransferase
  • AML
    acute myeloid leukaemia
  • AMP
    adenosine monophosphate
  • ANA
    antinuclear antibodies
  • ANAE
    alpha naphthyl acetate esterase
  • ANCA
    anti-neutrophilic cytoplasmic antibody
  • ANH
    acute normovolaemic haemodilution
  • APC
    activated protein C
  • APCR
    activated protein C resistance
  • APL
    antiphospholipid antibody
  • APML
    acute promyelocytic leukaemia
  • APS
    antiphospholipid syndrome
  • APTR
    activated partial thromboplastin ratio
  • APTT
    activated partial thromboplastin time
  • ARDS
    adult respiratory distress syndrome
  • ARF
    acute renal failure
  • ARMS
    amplification refractory mutation system
  • ASCT
    autologous stem cell transplantation
  • AST
    aspartate aminotranferase
  • AT (ATIII)
    antithrombin III
  • ATCML
    adult-type chronic myeloid (granulocytic) leukaemia
  • ATG
    anti-thymocyte globulin
  • ATLL
    adult T-cell leukaemia/lymphoma
  • ATP
    adenosine triphosphate
  • ATRA
    all-trans retinoic acid
  • A-V
    arteriovenous
  • AvWS
    acquired von Willebrand syndrome
  • β2-M
    beta-2-microglobuline
  • BAL
    broncho-alveolar lavage
  • B-CLL
    B-cell chronic lymphocytic leukaemia
  • bd
    bis die (twice daily)
  • BEAC
    BCNU, etoposide, cytosine, cyclophosphamide
  • BEAM
    BCNU, etoposide, cytarabine (ara-C), melphalan
  • BFU-E
    burst-forming unit-erythroid
  • BJP
    Bence Jones protein
  • BL
    Burkitt lymphoma
  • BM
    bone marrow
  • BMJ
    British Medical Journal
  • BMM
    bone marrow mastocytosis
  • BMT
    bone marrow transplantation
  • BNF
    British National Formulary
  • BP
    blood pressure
  • BPL
    BioProducts Laboratory
  • BSS
    Bernard–Soulier syndrome
  • BTG
    B-thromboglobulin
  • BU
    Bethesda Units
  • C/I
    consolidation/intensification
  • Ca
    carcinoma
  • Ca2+
    calcium
  • CABG
    coronary artery by pass graft
  • cALL
    common acute lymphoblastic leukaemia
  • CAMT
    congenital amegakaryocytic thrombocytopenia
  • CaPO4
    calcium phosphate
  • CBA
    collagen binding activity
  • CBV
    cyclophosphamide, carmustine (BCNU), etoposide
  • CCF
    congestive cardiac failure
  • CCR
    complete cytogenetic response
  • CD
    cluster differentiation or designation
  • CDA
    congenital dyserythropoietic anaemia
  • cDNA
    complementary DNA
  • CEL
    chronic eosinophilic leukaemia
  • CGL
    chronic granulocytic leukaemia
  • CHAD
    cold haemagglutinin disease
  • CHOP
    cyclophosphamide, adriamycin, vincristine, prednisolone
  • CJD
    Creutzfeldt–Jakob disease (v = variant)
  • Cl-
    chloride
  • CLD
    chronic liver disease
  • CLL
    chronic lymphocytic (‘lymphatic’) leukaemia
  • CM
    cutaneous mastocytosis
  • CMC
    chronic mucocutaneous candidiasis
  • CML
    chronic myeloid leukaemia
  • CMML
    chronic myelomonocytic leukaemia
  • CMV
    cytomegalovirus
  • CNS
    central nervous system
  • COAD
    chronic obstructive airways disease
  • COC
    combined oral contraceptive
  • COMP
    cyclophosphamide, vincristine, methotrexate,
  • CR
    complete remission
  • CRF
    chronic renal failure
  • CRP
    C-reactive protein
  • CRVT
    central retinal renous thrombosis
  • CSF
    cerebrospinal fluid
  • CT
    computed tomography
  • CTLp
    cytotoxic T-lymphocyte precursor assays
  • CTZ
    chemoreceptor trigger zone
  • CVA
    cerebrovascular accident
  • CVP
    cyclophosphamide, vincristine, prednisolone; central
  • CVS
    chorionic villus sampling
  • CVS
    cardiovascular system
  • CXR
    chest x-ray
  • CyA
    ciclosporin A
  • CytaBOM
    cytarabine, bleomycin, vincristine, methotrexate
  • d
    day
  • DAGT
    direct antiglobulin test
  • DAT
    direct antiglobulin test daunorubicin, cytosine (Ara-C),
  • dATP
    deoxy ATP
  • DBA
    Diamond–Blackfan anaemia
  • DC
    dyskeratosis congenita
  • DCS
    dendritic cell system
  • DCT
    direct Coombs’ test
  • DDAVP
    desamino D-arginyl vasopressin
  • DEAFF
    detection of early antigen fluorescent foci
  • DEB
    diepoxy butane
  • DFS
    disease-free survival
  • DHAP
    dexamethasone, cytarabine, cisplatin
  • DI
    delayed intensification
  • DIC
    disseminated intravascular coagulation
  • dL
    decilitre
  • DLBCL
    diffuse large B-cell lymphoma
  • DLI
    donor leucocyte/lymphocyte infusion
  • DMSO
    dimethyl sulphoxide
  • DNA
    deoxyribonucleic acid
  • DOB
    date of birth
  • DPG
    diphosphoglycerate
  • DRVVT
    dilute Russell’s viper venom time/test
  • DTT
    dilute thromboplastin time
  • DVT
    deep vein thrombosis
  • DXT
    radiotherapy
  • EACA
    epsilon aminocaproic acid
  • EBV
    Epstein–Barr virus
  • EBVP
    etoposide, bleomycin, vinblastine, prednisolone
  • ECG
    electrocardiograph
  • ECOG
    European Co-operative Oncology Group
  • EDTA
    ethylenediamine tetraacetic acid
  • EEC
    endogenous erythroid colonies
  • EFS
    event-free survival
  • EGF
    epidermal growth factor
  • ELISA
    enzyme-linked immunosorbent assay
  • EMEA
    European Medicines Agency
  • EMH
    extramedullary haemopoietic
  • EMU
    early morning urine
  • EPO
    erythropoietin
  • EPOCH
    etoposide, vincristine, doxorubicin, cyclophosphamide, prednisone
  • EPS
    electrophoresis
  • ESHAP
    etoposide, methylprednisolone, cytarabine, platinum
  • ESR
    erythrocyte sedimentation rate
  • ET
    essential thrombocythaemia or exchange transfusion
  • ETTL
    enteropathy type T-cell lymphoma
  • FAB
    French–American–British
  • FACS
    fluorescence-activated cell sorter
  • FBC
    full blood count
  • FCM
    fludarabine, cyclophosphamide, melphalan
  • FDG-PET
    18 fluoro–D–2–deoxyglucose positron emission tomography
  • FDP
    fibrin degradation products
  • Fe
    iron
  • FEIBA
    factor eight inhibitor bypassing activity
  • FEL
    familial erythrophagocytic lymphohistiocytosis
  • FeSO4
    ferrous sulphate
  • FFP
    fresh frozen plasma
  • FFS
    failure-free survival
  • Fgn
    fibrinogen
  • FH
    family history
  • FISH
    fluorescence in situ hybridisation
  • FITC
    fluorescein isothiocyanate
  • FIX
    factor IX
  • fL
    femtolitre
  • FL
    follicular lymphoma
  • FNA
    fine needle aspirate
  • FOB
    faecal occult blood
  • FVIII
    factor VIII
  • FVL
    factor V Leiden
  • g
    gram
  • G&S
    group, screen, and save
  • G6PD
    glucose-6-phosphate dehydrogenase
  • GA
    general anaesthetic
  • GCS
    graded compression stockings
  • G-CSF
    granulocyte colony stimulating factor
  • GIT
    gastrointestinal tract
  • GM-CSF
    granulocyte macrophage colony stimulating factor
  • GP
    glycoprotein
  • GPI
    glycosylphosphatidylinositol
  • GPS
    gray platelet syndrome
  • GT
    Glanzmann’s thrombasthenia
  • GvHD
    graft versus host disease
  • GvL
    graft versus leukaemia
  • h
    hour
  • H/LMW
    high/low molecular weight
  • HAART
    highly active antiretroviral therapy
  • HAV
    hepatitis A virus
  • Hb
    haemoglobin
  • HbA
    haemoglobin A
  • HbA2
    haemoglobin A2
  • HbF
    haemoglobin F (fetal Hb)
  • HbH
    haemoglobin H
  • HBsAg
    hepatitis B surface antigen
  • HBV
    hepatitis B virus
  • HC
    hydroxycarbamide or heavy chain
  • HCD
    heavy chain disease
  • HCG
    human chorionic gonadotrophin
  • HCII
    heparin cofactor II
  • HCL
    hairy cell leukaemia
  • HCO3
    bicarbonate
  • Hct
    haematocrit
  • HCV
    hepatitis C virus
  • HD
    haemodialysis
  • HDM
    high dose melphalan
  • HDN
    haemolytic disease of the newborn
  • HDT
    high dose therapy
  • HE
    hereditary elliptocytosis
  • HELLP
    haemolysis, elevated liver enzymes and low platelets
  • HES
    hypereosinophilic syndrome
  • HHT
    hereditary haemorrhagic telangiectasia
  • HI
    haematological improvement
  • HIT(T)
    heparin-induced thrombocytopenia (with thrombosis)
  • HIV
    human immunodeficiency virus
  • HL
    Hodgkin’s lymphoma (Hodgkin’s disease)
  • HLA
    human leucocyte antigen
  • HLH
    haemophagocytic lymphohistiocytosis
  • HMP
    hexose monophosphate shunt
  • HMWK
    high molecular weight kininogen
  • HPA
    human platelet antigen
  • HPF
    high power field
  • HPFH
    hereditary persistence of fetal haemoglobin
  • HPLC
    high performance liquid chromatography
  • HPP
    hereditary pyropoikilocytosis
  • HRT
    hormone replacement therapy
  • HS
    hereditary spherocytosis
  • HTLV-1
    human T-lymphotropic virus type 1
  • HTO
    high titre antibodies
  • HUMARA
    human androgen receptor gene assay
  • HUS
    haemolytic uraemic syndrome
  • IAGT
    indirect antiglobulin test
  • IAHS
    infection-associated haemophagocytic syndrome
  • ICE
    ifosfamide, carboplatin, etoposide
  • ICH
    intracranial haemorrhage
  • ICUS
    idiopathic cytopenia of uncertain (undetermined) significance
  • IDA
    iron deficiency anaemia
  • IF
    involved field (radiotherapy)
  • IFA
    intrinsic factor antibody
  • IFN-α
    interferon alpha
  • Ig
    immunoglobulin
  • IgA
    immunoglobulin A
  • IgD
    immunoglobulin D
  • IgE
    immunoglobulin E
  • IgG
    immunoglobulin G
  • IgM
    immunoglobulin M
  • IL-1
    interleukin-1
  • IM
    intramuscular
  • IMF
    idiopathic myelofibrosis
  • INR
    International normalized ratio
  • inv
    chromosomal inversion
  • IPC
    intermittent pneumatic compression devices
  • IPF
    immature platelet fraction
  • IPI
    International Prognostic Index
  • IPSS
    International Prognostic Scoring System
  • ISM
    Indolent systemic mastocytosis
  • ISS
    International Sensitivity Index
  • IT
    intrathecal
  • ITP
    idiopathic thrombocytopenic purpura
  • ITU
    Intensive Therapy Unit
  • IU
    international units
  • IUGR
    intrauterine growth retardation
  • IUT
    intrauterine transfusion
  • IV
    intravenous
  • IVI
    intravenous infusion
  • IVIg
    intravenous immunoglobulin
  • JCMML
    juvenile chronic myelomonocytic leukaemia
  • JML
    juvenile myelomonocytic leukaemia
  • JVP
    jugular venous pressure
  • KCT
    Kaolin clotting time
  • kg
    kilogram
  • L
    litre
  • LA
    lupus anticoagulant
  • LAP
    leucocyte alkaline phosphatase (score)
  • LC
    light chain
  • LCH
    Langerhans cell histiocytosis
  • LDH
    lactate dehydrogenase
  • LDHL
    lymphocyte depleted HL
  • LFS
    leukaemia free survival
  • LFTs
    liver function tests
  • LGL
    large granular lymphocyte
  • LLN
    lower limit of normal
  • LMWH
    low molecular weight heparin
  • LN
    lymph node(s)
  • LP
    lumbar puncture
  • LPD
    lymphoproliferative disorder
  • LRCHL
    lymphocyte rich classical HL
  • LSCS
    lower segment Caesarian section
  • LTC
    large transformed cells
  • M&P
    melphalan and prednisolone
  • MACOP-B
    methotrexate, doxorubicin, cyclophosphamide, vincristine, bleomycin, prednisolone
  • MAHA
    microangiopathic haemolytic anaemia
  • MALT
    mucosa-associated lymphoid tissue
  • m-BACOD
    methotrexate, bleomycin, adriamycin (doxorubicin), cyclophosphamide, vincristine, dexamethasone
  • mc
    micro
  • MC
    mast cell(s)
  • MCH
    mean cell haemoglobin
  • MCHC
    mean corpuscular haemoglobin concentration
  • MCHL
    mixed cellularity HL
  • MCL
    mast cell leukaemia or mantle cell lymphoma
  • MCP
    mitoxantrone, chlorambucil, prednisolone
  • MCR
    major cytogenetic response
  • MCS
    mast cell sarcoma
  • M-CSF
    macrophage colony stimulating factor
  • MCV
    mean cell volume
  • MDS
    myelodysplastic syndrome
  • MetHb
    methaemoglobin
  • MF
    myelofibrosis
  • mg
    milligram
  • MGUS
    monoclonal gammopathy of undetermined significance
  • MHC
    major histocompatibility complex
  • MI
    myocardial infarction
  • min
    minute(s)
  • mL
    millilitre
  • MLC
    mixed lymphocyte culture
  • MM
    multiple myeloma
  • MMC
    mitomycin C
  • MNC
    mononuclear cell(s)
  • MoAb
    monoclonal antibody
  • MP
    melphalan and prednisolone
  • MPCM
    maculopapular cutaneous mastocytosis
  • MPD
    myeloproliferative disease
  • MPO
    myeloperoxidase
  • MPS
    mononuclear phagocytic system
  • MPT
    melphalan, prednisolone, and thalidomide
  • MPV
    mean platelet volume
  • MRD
    minimal residual disease
  • MRI
    magnetic resonance imaging
  • mRNA
    messenger ribonucleic acid
  • MRSA
    meticillin-resistant Staphylococcus aureus
  • MSBOS
    maximum surgical blood ordering schedule
  • MSU
    midstream urine
  • MT
    mass: thoracic
  • MTX
    methotrexate
  • MUD
    matched unrelated donor (transplant)
  • MZL
    mantle zone lymphoma
  • Na+
    sodium
  • NaCl
    sodium chloride
  • NADP
    nicotinamide adenine diphosphate
  • NADPH
    nicotinamide adenine diphosphate (reduced)
  • NAIT
    neonatal alloimmune thrombocytopenia
  • NAP
    neutrophil alkaline phosphatase
  • NBT
    nitro blue tetrazolium
  • NEJM
    New England Journal of Medicine
  • NHL
    non-Hodgkin’s lymphoma
  • NLPHL
    nodular lymphocyte predominant HL
  • NRBC
    nucleated red blood cells
  • NS
    nodular sclerosing
  • NS
    non-secretory (myeloma)
  • NSAIDs
    non-steroidal antiinflammatory drugs
  • NSE
    non-specific esterase
  • NSHL
    nodular sclerosing HL
  • OAF
    OC-activating factor
  • OB
    osteoblast
  • OC
    osteoclast
  • OCP
    oral contraceptive pill
  • od
    omni die (once daily)
  • OPG
    osteoprotogerin
  • OPG
    orthopantomogram
  • OR
    overall response
  • OS
    overall survival
  • OWR
    Osler–Weber–Rendu
  • PA
    pernicious anaemia
  • PAI
    plasminogen activator inhibitor
  • PaO2
    partial pressure of O2 in arterial blood
  • PAS
    periodic acid–Schiff
  • PB
    peripheral blood
  • PBSC
    peripheral blood stem cell
  • PC
    protein C
  • PCC
    prothrombin complex concentrate
  • PCH
    paroxysmal cold haemoglobinuria
  • PCL
    plasma cell leukaemia
  • PCP
    Pneumocystis carinii pneumonia
  • PCR
    polymerase chain reaction
  • PCV
    packed cell volume
  • PD
    peritoneal dialysis
  • PDGF
    platelet-derived growth factor
  • PDW
    platelet distribution width
  • PE
    pulmonary embolism
  • PEP
    post-expoure prophylaxis
  • PET
    pre-eclamptic toxaemia or position emission tomography
  • PF
    platelet factor
  • PFA
    platelet function analysis
  • PFK
    phosphofructokinase
  • PFS
    progression-free survival
  • PGD2
    prostaglandin D2
  • PGE1
    prostaglandin E1
  • PGK
    phosphoglycerate kinase
  • Ph
    Philadelphia chromosome
  • PIG
    phosphatidylinositol glycoproteins
  • PIVKA
    protein induced by vitamin K absence
  • PK
    pyruvate kinase
  • PLL
    prolymphocytic leukaemia
  • PML
    promyelocytic leukaemia
  • PNET
    primitive neuroectodermal tumour
  • PO
    per os (by mouth)
  • PPH
    post-partum haomorrhage
  • PPI
    proton pump inhibitor
  • PPP
    primary proliferative polycythaemia
  • PRCA
    pure red cell aplasia
  • PRN
    as required
  • ProMACE
    prednisolone, doxorubicin, cyclophosphamide, etoposide
  • PRV
    polycythaemia rubra vera
  • PS
    protein S
  • PSA
    pure sideroblastic anaemia or prostate-specific antigen
  • PT
    prothrombin time
  • PTCL
    peripheral T-cell lymphomas
  • PTP
    pretest probability or post-transfusion purpura
  • PUVA
    phototherapy with psoralen plus UV-A
  • PV
    polycythaemia vera
  • PVO
    pyrexia of unknown origin
  • qds
    quater die sumendus (to be taken 4 times a day)
  • QoL
    quality of life
  • RA
    refractory anaemia
  • RAEB
    refractory anaemia with excess blasts
  • RAEB-t
    refractory anaemia with excess blasts in transformation
  • RAR
    retinoic acid receptor
  • RARS
    refractory anaemia with ring sideroblasts
  • RBC
    red blood cell
  • RCC
    red blood cell count
  • RCM
    red cell mass
  • RCMD
    refractory cytopenia with multilineage dysplasia
  • RDS
    respiratory distress syndrome
  • RDW
    red cell distribution width
  • RE
    relative erythrocytosis; reticuloendothelial
  • REAL
    Revised European American Lymphoma
  • RES
    reticuloendothelial system
  • RFLP
    restriction fragment length polymorphism
  • Rh
    Rhesus
  • rhAPC
    recombinant human activated protein C
  • rhG-CSF
    recombinant human granulocyte colony stimulating factor
  • rHuEPO
    recombinant human erythropoietin
  • RI
    remission induction
  • RIA
    radioimmunoassay
  • RIC
    reduced-intensity conditioning
  • RiCoF
    ristocetin cofactor
  • RIPA
    ristocetin-induced platelet agglutination
  • RS
    Reed–Sternberg or ringed sideroblasts
  • RT
    reptilase time
  • RT-PCR
    reverse transcriptase polymerase chain reaction
  • s
    second(s)
  • SAA
    serum amyloid A protein
  • SAGM
    saline adenine glucose mannitol
  • SaO2
    arterial oxygen saturation
  • SAP
    serum amyloid P protein
  • SBP
    solitary plasmacytoma of bone
  • SC
    subcutaneous
  • SCA
    sickle cell anaemia
  • SCBU
    special care baby unit
  • SCD
    sickle cell disease
  • SCID
    severe combined immunodeficiency
  • SCT
    stem cell transplantation or silica clot time
  • SD
    standard deviation
  • SE
    secondary erythrocytosis
  • SEP
    extramedullary plasmacytoma
  • SLE
    systemic lupus erythematosus
  • SLL
    small lymphocytic lymphoma
  • SLVL
    splenic lymphoma with villous lymphocytes
  • SM
    systemic mastocytosis
  • SM-AHNMD
    systemic mastocytosis with an associated clonal haemato logical non-mast cell lineage disease
  • SmIg
    surface membrane immunoglobulin
  • SMZL
    splenic marginal zone lymphoma
  • SOB
    short of breath
  • SPB
    solitary plasmacytoma of bone
  • SPD
    storage pool disorders/deficiency
  • stat
    statim (immediate; as initial dose)
  • sTfR
    soluble transferrin receptor
  • SVC
    superior vena cava
  • SVCO
    superior vena caval obstruction
  • T° (4T°)
    temperature (fever)

  • half-life
  • T4
    thyroxine
  • TAM
    transient abnormal myelopoiesis
  • TAR
    thrombocytopenia with absent radius
  • TB
    tuberculosis
  • TBI
    total body irradiation
  • TCR
    T-cell receptor
  • tds
    ter die sumendum (to be taken 3 times a day)
  • TdT
    terminal deoxynucleotidyl transferase
  • TEC
    transient erythroblastopenia of childhood
  • TEG
    thromboelastography
  • TENS
    transcutaneous nerve stimulation
  • TF
    tissue factor
  • TFT
    thyroid function test(s)
  • TGF-β
    transforming growth factor-β
  • TI
    transfusion-independence
  • TIAs
    transient ischaemic attacks
  • TIBC
    total iron binding capacity
  • tiw
    three times in a week
  • TNF
    tumour necrosis factor
  • topo II
    topoisomerase II
  • TORCH
    toxoplasmosis, rubella, cytomegalovirus, herpes sim
  • TPA
    tissue plasminogen activator
  • TPI
    triphosphate isomerase
  • TPN
    total parenteral nutrition
  • TPO
    thrombopoietin
  • TPR
    temperature, pulse, respiration
  • TRAP
    tartrate-resistant acid phosphatase
  • TRM
    treatment related mortality
  • TSE
    transmissible spongiform encephalopathy
  • TSH
    thyroid-stimulating hormone
  • TT
    thrombin time
  • TTP
    thrombotic thrombocytopenic purpura
  • TXA
    tranexamic acid
  • TXA2
    thromboxane A2
  • U&E
    urea and electrolytes
  • U
    unit(s)
  • UC
    ulcerative colitis
  • UFH
    unfractionated heparin
  • URTI
    upper respiratory tract infection
  • US
    ultrasound
  • USS
    ultrasound scan
  • UTI
    urinary tract infection
  • VAD
    vincristine adriamycin dexamethasone regimen
  • VBAP
    vincristine, carmustine (BCNU), doxorubicin, prednisolone
  • VBMCP
    vincristine, carmustine, melphalan, cyclophosphamide, prednisolone
  • VC
    vena cava
  • VDRL
    Venereal Disease Research Laboratory
  • VEGF
    vascular endothelial growth factor
  • VF
    ventricular fibrillation
  • VIII:C
    factor VIII clotting activity
  • Vit K
    vitamin K
  • VMCP
    vincristine, melphalan, cyclophosphamide, prednisolone
  • VMP
    melphalan, prednisolone, bortezomib
  • VOD
    veno-occlusive disease
  • VTE
    venous thromboembolism
  • vWD
    von Willebrand disease
  • vWF
    von Willebrand factor
  • vWFAg
    von Willebrand factor antigen
  • WAS
    Wiskott–Aldrich syndrome
  • WBC
    white blood cell
  • WBRT
    whole brain radiotherapy
  • WCC
    white cell count
  • WM
    Waldenström macroglobulinaemia
  • X match
    cross-match
  • XDPs
    cross-linked fibrin degradation products






DOI: 10.1093/med/9780199227396.002.0013

3rd edition

The Oxford Handbook of Clinical Haematology continues to provide the core knowledge needed in clinical practice for the diagnosis and management of patients with disorders of the blood. Major advances in the specialty have been reflected in this thoroughly revised content. Differential diagnoses, relevant investigations and management guidelines are covered.

Disclaimer

Oxford University Press makes no representation, express or implied, that the drug dosages in this book are correct. Readers must therefore always check the product information and clinical procedures with the most up to date published product information and data sheets provided by the manufacturers and the most recent codes of conduct and safety regulations. The authors and the publishers do not accept responsibility or legal liability for any errors in the text or for the misuse or misapplication of material in this work.

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