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진료과

  • 의과대학-진단검사의학교실, 진단검사의학과

전문진료분야

  • 진단혈액학, 혈전지혈, 혈액종양학

교육 및 임상 경력

  • 2002  -  2004년  연세의대  연구강사
  • 2004  -  2005년  용인세브란스병원  진단검사의학과장

학술관련경력

  • 대한진단검사의학회
  • 대한혈액학회
  • 대한혈전지혈학회

주요 관심분야

  • 혈전지혈 질환
  • 골수이형성 증후군
  • 급성 골수구성 백혈병
  • 기타 혈액종양

학력사항

  • 연세대학교 의학과 학사 (1997년)
  • 연세대학교 의학과 석사 (2000년)

논문

  • Measurement of thrombus precursor protein in septic patients with disseminated intravascular coagulation and liver disease
    HAEMATOLOGICA-THE HEMATOLOGY JOURNAL 87/10 :1062-1067,2002
  • Plasma factor XIII activity in patients with disseminated intravascular coagulation
    YONSEI MEDICAL JOURNAL 47/2 :196-200,2006
  • Plasma level of IL-6 and its relationship to procoagulant and fibrinolytic markers in acute ischemic stroke
    YONSEI MEDICAL JOURNAL 47/2 :201-206,2006
  • 늑막삼출과 주변 림프절 침범이 동반된 다발성골수종 1예
    대한혈액학회지 41/1 :6-6,2006
  • t(5;12)(q13;p13) in acute myeloid leukemia with preceding granulocytic sarcoma
    CANCER GENETICS AND CYTOGENETICS 177/2 :158-160,2007
  • 자동혈구분석기 Cell-Dyn Sapphire의 평가
    대한진단검사의학회지(The Korean Journal of Laboratory Medicine) 27/3 :162-168,2007
  • 한국 von Willebrand병 환자의 von Willebrand 인자 유전자 돌연변이 조사
    대한진단검사의학회지(The Korean Journal of Laboratory Medicine) 27/3 :169-176,2007
  • Anti-PF4/Heparin 항체 양성의 헤파린 유도 혈소판감소증 1예
    대한혈액학회지 42/1 :10-10,2007
  • A der(1;15)(q10;q10) is a rare nonrandom whole-arm translocation in patients with acute lymphoblastic leukemia
    CANCER GENETICS AND CYTOGENETICS 179/2 :132-135,2007
  • Diagnosis of overt disseminated intravascular coagulation: A comparative study using criteria from the international society versus the Korean Society on Thrombosis and Hemostasis
    YONSEI MEDICAL JOURNAL 48/4 :595-600,2007
  • Preceding orbital granulocytic sarcoma in an adult patient with acute myelogenous leukemia with t(8;21): a case study and review of the literature
    Cancer Genetics And Cytogenetics 185/ :51-54,2008
  • Complex t(8;1.9;21)(q22;p13;q22) as a sole abnormality in a patient with de novo acute myeloid leukemia
    Cancer Genetics And Cytogenetics 185/ :109-112,2008
  • Acute erythroleukemia with der(1;7)(q10;p10) as a sole acquired abnormality after treatment with azathioprine
    Cancer Genetics And Cytogenetics 186/ :58-60,2008
  • Linear Relationship between ADAMTS13 Activity and Platelet Dynamics Even Before Severe Thrombocytopenia
    Annals Of Clinical And Laboratory Science 38/ :368-375,2008
  • Transfusion-associated iron overload as a predictive factor for poor stem cell mobilization in patients with haematological malignancies
    Transfusion Medicine 18/ :97-103,2008
  • Analysis of clinical presentations of Bruton Disease: A review of 20 years of accumulated data from pediatric patients at Severance Hospital
    Yonsei Medical Journal 49/1 :28-36,2008
  • Rare translocations involving chromosome band 8p11 in myeloid neoplasms
    Cancer Genetics And Cytogenetics 186/ :127-129,2008
  • Trisomy 8 in an elderly patient with acute lymphoblastic leukemia as a sole abnormality
    Cancer Genetics And Cytogenetics 187/ :57-58,2008
  • 듀센형근이영양증 유전자의 결실 돌연변이 검출을 위한 Dual Priming Oligonucleotide 다중 PCR법의 평가
    Korean Journal Of Laboratory Medicine 28/5 :386-391,2008
  • Acute promyelocytic leukemia relapsing as secondary acute myelogenous leukemia with translocation t(3;21)(q26;q22) and RUNX1-MDS1-EVI1 fusion transcript
    Cancer Genetics And Cytogenetics 187/2 :61-73,2008
  • A novel missense MSH2 gene mutation in a patient of a Korean family with hereditary nonpolyposis colorectal cancer
    Cancer Genetics And Cytogenetics 182/2 :136-139,2008
  • 8번 염색체 사체성을 보인 급성단구성백혈병 1예
    Korean Journal Of Laboratory Medicine 28/4 :262-266,2008
  • Paracentric inversion-associated t(8;21) variant in de novo acute myelogenous leukemia: characteristic patterns of conventional cytogenetics, FISH, and multicolor banding analysis
    Cancer Genetics And Cytogenetics 183/1 :72-76,2008
  • 8p11 myeloproliferative syndrome preceded by t(8;9)(p11;q33), CEP110/FGFR1 fusion transcript: morphologic, molecular, and cytogenetic characterization of myeloid neoplasms associated with eosinophilia and FGFR1 abnormality
    Cancer Genetics And Cytogenetics 181/ :93-99,2008
  • MLL rearrangement with t(6;11)(q15;q23) as a sole abnormality in a patient with de novo acute myeloid leukemia: conventional cytogenetics, FISH, and multicolor FISH analyses for detection of rare MLL-related chromosome abnormalities
    Cancer Genetics And Cytogenetics 187/ :50-53,2008
  • Transfusion-Associated Iron Overload as an Adverse Risk Factor for Transplantation Outcome in Patients Undergoing Reduced-Intensity Stem Cell Transplantation for Myeloid Malignancies
    Acta Haematologica 120/3 :182-189,2008
  • Three new nonsense mutations of MLH1 and MSH2 genes in Korean families with hereditary nonpolyposis colorectal cancer
    Cancer Genetics and Cytogenetics 188/ :61-64,2009
  • Acute promyelocytic leukemia with insertion of PML exon 7a and partial deletion of exon 3 of RARA: a novel variant transcript related to aggressive course and not detected with real-time polymerase chain reaction analysis
    Cancer Genetics and Cytogenetics 188/ :103-107,2009
  • Biphenotypic acute leukemia with b2a2 fusion transcript and trisomy 21
    Cancer Genetics and Cytogenetics 188/ :129-131,2009
  • Acute promyelocytic leukemia in early pregnancy with translocation t(15;17) and variant PML/RARA fusion transcripts
    Cancer Genetics and Cytogenetics 188/ :48-51,2009
  • JAK2 V617F/C618R mutation in a patient with polycythemia vera: A case study and review of the literature
    Cancer Genetics and Cytogenetics 189/ :43-47,2009
  • Hereditary protein S deficiency from a novel large deletion mutation of the PROS1 gene detected by multiplex ligation-dependent probe amplification (MLPA)
    Thrombosis Research 123/5 :793-795,2009
  • A novel in-frame deletion in the factor V C1 domain associated with severe coagulation factor V deficiency in a Korean family
    Blood Coagulation & Fibrinolysis 20/ :150-156,2009
  • Therapy-Related Myelodysplastic Syndrome/Acute Myeloid Leukemia after Treatment with Temozolomide in a Patient with Glioblastoma Multiforme
    Annals Of Clinical And Laboratory Science 39/4 :392-398,2009
  • Therapy-related acute lymphoblastic leukemia with t(9;22)(q34;q11.2): a case study and review of the literature
    Cancer Genetics and Cytogenetics 191/ :51-54,2009
  • Concomitant Isochromosome 17q and Trisomy 14 in a Patient with Myelodysplastic Syndrome in Leukemic Transformation
    Annals Of Clinical And Laboratory Science 39/2 :176-181,2009
  • A Novel PHEX Mutation in a Korean Patient with Sporadic Hypophosphatemic Rickets
    Annals Of Clinical And Laboratory Science 39/2 :182-187,2009
  • Two case reports of 1q triplication in myeloproliferative neoplasms
    Cancer Genetics and Cytogenetics 191/2 :111-112,2009
  • Non-age related Y chromosome loss in an elderly patient with acute promyelocytic leukemia
    Leukemia Research 33/ :e114-e115,2009
  • der(1)t(1;19)(p13;p13.1) in two elderly patients with myeloid neoplasms: New case reports and review of the literature
    Leukemia Research 33/8 :128-131,2009
  • Concomitant t(3;3)(q21;q26), trisomy 19, and E255V mutation associated with imatinib mesylate resistance in chronic myelogenous leukemia
    Cancer Genetics and Cytogenetics 190/ :46-48,2009
  • Detection of a novel CBFB/MYH11 variant fusion transcript (K-type) showing partial insertion of exon 6 of CBFB gene using two commercially available multiplex RT-PCR kits
    Cancer Genetics and Cytogenetics 189/2 :87-92,2009
  • A tandem triplication, trp(1)(q21q32), in a patient with follicular lymphoma: a case study and review of the literature
    Cancer Genetics and Cytogenetics 189/ :127-131,2009
  • BCR/ABL rearrangement with b3a3 fusion transcript in a case of childhood acute lymphoblastic leukemia
    Cancer Genetics and Cytogenetics 189/ :132-137,2009
  • Chronic Myelomonocytic Leukemia with der(9)t(1;9)(q11;q34) as a Sole Abnormality
    Annals Of Clinical And Laboratory Science 39/3 :307-312,2009
  • Detection of FUS-ERG chimeric transcript in two cases of acute myeloid leukemia with t(16;21)(p11.2;q22) with unusual characteristics
    Cancer Genetics and Cytogenetics 194/2 :111-118,2009
  • CASP8AP2 is a novel partner gene of MLL rearrangement with t(6;11)(q15;q23) in acute myeloid leukemia
    Cancer Genetics and Cytogenetics 195/1 :94-95,2009
  • Therapy-related myelodysplastic syndrome with der(17)t(12;17)(q13;p13) as a new recurrent cytogenetic abnormality after treatment for chronic lymphocytic leukemia
    Leukemia Research 33/7 :1001-1004,2009
  • Association between acute promyelocytic leukemia and ring chromosome 6
    Cancer Genetics and Cytogenetics 192/1 :48-50,2009
  • Three-way translocation involving MLL, MLLT1, and a novel third partner, NRXN1, in a patient with acute lymphoblastic leukemia and t(2;19;11) (p12;p13.3;q23)
    Cancer Genetics and Cytogenetics 197/1 :32-38,2010
  • A novel t(1;12)(q21;q24) in a patient with myelodysplastic syndrome
    Annals of Hematology 89/ :513-516,2010
  • Short Report: Automated Detection of Malaria-Associated Pseudoeosinophilia and Abnormal WBC Scattergram by the Sysmex XE-2100 Hematology Analyzer: A Clinical Study with 1,801 Patients and Real-Time Quantitative PCR Analysis in Vivax Malaria-Endemic
    American Journal of Tropical Medicine and Hygiene 82/3 :412-414,2010
  • Agranular platelets as a cardinal feature of ARC syndrome
    Journal Of Pediatric Hematology Oncology 32/4 :253-258,2010
  • An SRY-Deleted XXY Female Resulting from a Paternally Inherited t(Y;22)
    Annals of Clinical and Laboratory Science 40/3 :295-299,2010
  • Molecular characterization of alternative SET-NUP214 fusion transcripts in a case of acute undifferentiated leukemia
    Cancer Genetics and Cytogenetics 201/2 :73-80,2010
  • Prognostic significance of trisomy 6 in an adult acute myeloid leukemia with t(8;21)
    Cancer Genetics and Cytogenetics 202/2 :141-143,2010
  • Constitutional pericentric inversion 9 and hematological disorders: a Korean tertiary institution's experience over eight years
    Annals of Clinical and Laboratory Science 40/3 :273-277,2010
  • Constitutional Pericentric Inversion 9 in Korean Patients with Chronic Myelogenous Leukemia
    KOREAN JOURNAL OF LABORATORY MEDICINE 30/3 :218-223,2010
  • Comparison of Effects of Two Different Formulations of Clopidogrel Bisulfate Tablets on Platelet Aggregation and Bleeding Time in Healthy Korean Volunteers: A Single-Dose, Randomized, Open-Label, 1-Week, Two-Period, Phase IV Crossover Study
    Clinical Therapeutics 32/9 :1664-1673,2010
  • Molecular cytogenetic analysis of Korean patients with Waldenstrom macroglobulinemia
    Cancer Genetics and Cytogenetics 197/2 :117-121,2010
  • Diagnosis of non-overt disseminated intravascular coagulation made according to the International Society on Thrombosis and Hemostasis criteria with some modifications
    대한혈액학회지 45/4 :260-263,2010
  • Case Report: A Heparin Binding Site Arg79Cys Missense Mutation in the SERPINC1 Gene in a Korean Patient with Hereditary Antithrombin Deficiency
    ANNALS OF CLINICAL AND LABORATORY SCIENCE 41/1 :89-92,2011
  • Rapid Identification of Thrombocytopenia-Associated Multiple Organ Failure Using Red Blood Cell Parameters and a Volume/Hemoglobin Concentration Cytogram
    YONSEI MEDICAL JOURNAL 52/5 :845-850,2011
  • Acute Promyelocytic Leukemia with Trisomy 8 and del(9)(q22) after Treatment of Cervical Cancer with Concurrent Chemoradiotherapy: A Case Report
    ONKOLOGIE 34/7 :388-390,2011
  • DELTA NEUTROPHIL INDEX: A PROMISING DIAGNOSTIC AND PROGNOSTIC MARKER FOR SEPSIS
    SHOCK 37/ :242-246,2012
  • Population-specific spectrum of the F11 mutations in Koreans: evidence for a founder effect
    CLINICAL GENETICS 82/2 :180-186,2012
  • CD5-negative Blastoid Variant Mantle Cell Lymphoma with Complex CCND1/IGH and MYC Aberrations
    ANNALS OF LABORATORY MEDICINE 32/1 :95-98,2012
  • Fibrinogen residue gamma Ala341 is necessary for calcium binding and 'A-a' interactions
    THROMBOSIS AND HAEMOSTASIS 107/5 :875-883,2012
  • Comparison Study of the Rates of Manual Peripheral Blood Smear Review From 3 Automated Hematology Analyzers, Unicel DxH 800, ADVIA 2120i, and XE 2100, Using International Consensus Group Guidelines
    ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE 136/11 :1408-1413,2012
  • A Gly1609Arg Missense Mutation in the vWF Gene in a Korean Patient with von Willebrand Disease Type 2A
    ANNALS OF CLINICAL AND LABORATORY SCIENCE 42/1 :98-102,2012
  • Image analysis of peripheral compression artefacts of ThinPrep? liquid-based cytology preparations
    CYTOPATHOLOGY 24/2 :99-104,2013
  • Immature platelet fraction in diabetes mellitus and metabolic syndrome
    THROMBOSIS RESEARCH 132/6 :692-695,2013
  • The instability of commercial control materials in quality control of mean corpuscular volume
    CLINICA CHIMICA ACTA 434/- :11-15,2014
  • Analytical and clinical performance of a new point of care LABGEOIB D-dimer test for diagnosis of venous thromboembolism
    ANNALS OF CLINICAL AND LABORATORY SCIENCE 44/3 :254-261,2014
  • Monoclonal and polyclonal gammopathy measured by serum free light chain and immunofixation subdivide the clinical outcomes of diffuse large B-cell lymphoma according to molecular classification
    ANNALS OF HEMATOLOGY 93/11 :1867-1877,2014
  • Comparison of Prothrombin Time Derived From CoaguChek XS and Laboratory Test According to Fibrinogen Level
    JOURNAL OF CLINICAL LABORATORY ANALYSIS 29/1 :28-31,2015
  • Quantitative Influence of ABO Blood Groups on Factor VIII and Its Ratio to von Willebrand Factor, Novel Observations from an ARIC Study of 11,673 Subjects
    PLOS ONE 10/8 :e0132626-,2015
  • Capillary-scale direct measurement of hemoglobin concentration of erythrocytes using photothermal angular light scattering
    BIOSENSORS & BIOELECTRONICS 74/ :469-475,2015
  • Selective serotonin reuptake inhibitors facilitate ANO6 (TMEM16F) current activation and phosphatidylserine exposure
    PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY 467/11 :2243-2256,2015
  • Pretreatment Lymphopenia, Poor Performance Status, and Early Courses of Therapy Are Risk Factors for Severe Bacterial Infection in Patients with Multiple Myeloma during Treatment with Bortezomib-based Regimens
    JOURNAL OF KOREAN MEDICAL SCIENCE 31/4 :510-518,2016
  • The prognostic significance of monoclonal immunoglobulin gene rearrangement in conjunction with histologic B-cell aggregates in the bone marrow of patients with diffuse large B-cell lymphoma
    CANCER MEDICINE 5/6 :1066-1073,2016
  • Magnetic bead-based nucleic acid purification kit: Clinical application and performance evaluation in stool specimens
    JOURNAL OF MICROBIOLOGICAL METHODS 124/ :62-68,2016
  • Association of Single Nucleotide Polymorphisms in the ST3GAL4 Gene with VWF Antigen and Factor VIII Activity
    PLOS ONE 11/9 :e0160757-,2016
  • Clinical Utility of Bone Marrow Study in Gaucher Disease: A Case Report of Gaucher Disease Type 3 With Intractable Myoclonic Seizures
    ANNALS OF LABORATORY MEDICINE 36/2 :177-179,2016
  • Automated CH50 liposome-based immunoassay: consideration in dilution and validation of reference interval
    CLINICAL CHEMISTRY AND LABORATORY MEDICINE 54/10 :e309-e312,2016
  • Neutrophil to lymphocyte ratio and platelet to lymphocyte ratio as diagnostic markers for pneumonia severity
    BRITISH JOURNAL OF BIOMEDICAL SCIENCE 73/3 :140-142,2016
  • A Rapid and Chemical-free Hemoglobin Assay with Photothermal Angular Light Scattering
    JOVE-JOURNAL OF VISUALIZED EXPERIMENTS 118/e5500 :1-6,2016
  • Smart Forensic Phone: Colorimetric analysis of a bloodstain for age estimation using a smartphone
    SENSORS AND ACTUATORS B-CHEMICAL 243/ :221-225,2017
  • Color-coded LED microscopy for quantitative phase imaging: Implementation and application to sperm motility analysis
    METHODS 136/ :66-74,2018
  • Platelet storage induces accelerated desialylation of platelets and increases hepatic thrombopoietin production
    JOURNAL OF TRANSLATIONAL MEDICINE 16/1 :199-208,2018
  • HBsAg-Negative, Anti-HBc?Negative Patients Still Have a Risk of Hepatitis B Virus?Related Hepatitis after Autologous Stem Cell Transplantation for Multiple Myeloma or Malignant Lymphoma
    CANCER RESEARCH AND TREATMENT 50/4 :1,121-1,129,2018
  • Biometric Image Analysis for Quantitation of Dividing Platelets
    MICROMACHINES 10/1 :1-13,2018
  • Highly sensitive and accurate estimation of bloodstain age using smartphone
    BIOSENSORS & BIOELECTRONICS 130/ :414-419,2019

송재우

진료철학
질병의 진단은 의사의 오감을 통해 얻은 정보와 예상을 관련 검사로 확인하는 일련의 과정이다. 진단검사의학은 환자의 혈액이나 체액 등의 검체로부터 질병의 진단과 경과 추적에 필요한 객관적인 검사 결과를 제공하는 의학 분야로 의학이 과학으로 인정받을 수 있게 하는 초석이라 할 수 있다. 그러므로, 합리적인 임상 검사실 운영을 통한 신뢰할 수 있는 검사 결과 도출은 환자의 진료에 있어 빼놓을 수 없는 핵심이라 할 수 있다. 특히 혈액학 파트는 검사 결과가 환자의 치료에 직접적인 영향을 끼치는 검사들이 매우 많은 분야이다. 안으로 효과적인 검사실 내부정도관리와 교육, 밖으로는 지속적인 임상과의 대화와 엄격한 외부정도관리만이 질 높은 검사실을 유지해 나갈 수 있는 방도임을 유념하고 실행하며, 끊임없이 새롭고 유용한 검사들을 개발 도입함으로써 발전의 궤를 멈추지 않을 것이다.

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