• 검색 결과가 없습니다.

Complete Blood Count

N/A
N/A
Protected

Academic year: 2022

Share "Complete Blood Count"

Copied!
10
0
0

로드 중.... (전체 텍스트 보기)

전체 글

(1)

Complete Blood Count

임상에서 가장 흔히 시행되는 검사

• 임상에서 가장 흔히 시행되는 검사

• 혈액학적 평가의 기본검사혈액학적 평가의 기본검사

• 골수 기능에 대한 정보 제공

• 혈액질환의 진단에 중요한 정보 제공

• 혈액질환의 진단에 중요한 정보 제공

• 현재 완전 자동화 되어있고 재현성이 높음

(2)

Differential Diagnosis Of Anemia Differential Diagnosis Of Anemia

Use MCV and RDW

Low MCV Normal MCV High MCV

RDW<15 Th l i t it ACD A l ti i

RDW<15 Thalassemia trait Hetero HbE, HbC, Anemia of chronic

ACD

Heterozygous HbS, HbCS, HbE

Aplastic anemia MDS

Myeloma disease (ACD) H. spherocytosis

Acute hemorrhage

Liver disease Hyperthyroidism RDW>15 Iron deficiency anemia Early or combined B12 deficiency RDW>15 Iron deficiency anemia

Thalassemia intermedia Sideroblastic anemia

S ACD

Early or combined nutritional deficiency Myelodysplasia

M l hthi i

B12 deficiency Folate deficiency AIHA

D HU ARV

Severe ACD

RBC fragmentation

Myelophthisis

Sickle cell anemia Homozygous HbCS

Drugs: HU, ARV, AZA, etc.

(3)

Erythrocytosis (Hb>18 (M), Hb>16 (F))

Primary (low EPO)

Erythrocytosis (Hb 18 (M), Hb 16 (F))

Primary (low EPO)

Polycythemia vera Secondary (high EPO) Secondary (high EPO)

High affinity hemoglobin

Hypoxia : COPD cyanotic heart disease Hypoxia : COPD, cyanotic heart disease,

sleep apnea, high altitude Inapproate erythropoietin synthesis Inapproate erythropoietin synthesis

Renal disease : renal cell carcinoma, PCKD RA stenosis, post-transplant polycythemia, p p p y y Others : cerebellar hemangioblastoma,

hepatoma, myoma, meningioma, p y g Cushing's syndrome, androgen

(4)

Inaccurate Estimates Of Hb RBC MCV Inaccurate Estimates Of Hb, RBC, MCV

High Hb High WBC, hyperlipidemia, paraproteinemia, cryoglobulinemia

High RBC High WBC, Numerous large platelets, hyperlipidemia, cryoglobulinemia

Low RBC Cold agglutinin, EDTA-dependent agglutination,

f C

extreme microcytosis, fragmented RBC

High MCV Storage at RT, cold agglutinin, EDTA-dependent l ti ti hi h WBC h l it

agglutination, high WBC, hyperosmolarity

Low MCV Hypochromic red cell, increased temperature, h po osmaolarit

hypo-osmaolarity

(5)

Neutropenia

Infection Viral (measles mumps rubella)

Neutropenia

Infection Viral (measles, mumps, rubella)

Bacterial (typhoid, Gram (-) infection) Rickettsial

Rickettsial

Drugs Chemotherapy, antithyroid drugs,

sulphonamide vancomycin cephalosporine sulphonamide, vancomycin, cephalosporine phenytoin, valproate, chlorpromazine,

interferon, rituximab, imatinib interferon, rituximab, imatinib Radiation therapy

Aplastic anemiap

Autoimmune neutropenia Cyclical neutropeniay p

Constitutional (idopathic) Alcoholism

(6)

Mild Thrombocytopenia (>80K)

I f ti (VIRAL b t i l)

Mild Thrombocytopenia (>80K)

Infection (VIRAL, bacterial) Drugs

tibi ti NSAID ti l ti i tidi

antibiotics, NSAID, antineoplastics, cimetidine, phenytoin, valproic acid, thiazide

Chronic alcoholism Chronic alcoholism

Autoimmune disease (SLE) Hypersplenism

Hypersplenism

(7)

Marked Thrombocytosis

Myeloproliferative neoplasm Malignant disease

Post-splenectomy p y Infection

Inflammation Inflammation

Connective tissue disorder Iron deficiency

Iron deficiency

Trauma or tissue damage

(8)

P t i

Fanconi's anemia

Pancytopenia

Fanconi s anemia

Aplastic anemia, PNH

Bone marrow infiltration of malignant cells Bone marrow infiltration of malignant cells

Acute leukemia, myeloma, carcinoma, lymphoma Myelodysplastic syndrome

Myelodysplastic syndrome Idiopathic myelofibrosis

Acquired immune deficiency syndrome(AIDS) Acquired immune deficiency syndrome(AIDS) Graft-versus-host disease

Drugsg

Chemotherapy, PAS, sulfonamide, rifampicin Hypersplenismyp p

Alcohol toxicity

(9)

I di ti f BM i ti

Indication of BM examination

• Suspected hematologic disorder

• Leukopenia of unknown cause Leukopenia of unknown cause

• Thrombocytopenia of unknown cause

• Anemia of unknown cause

• Anemia of unknown cause

• Bicytopenia

P t i

• Pancytopenia

• Leukoerythroblastosis

• Abnormal cells in peripheral blood

• Staging work up for malignancy g g p g y

• Work up for fever of unknown origin

(10)

결 론 결 론

1.CBC는 혈액질환의 선별검사로서 유용하다.

2 CBC 검사 결과를 해석할 때 검사에서 발생 2.CBC 검사 결과를 해석할 때 검사에서 발생

할 수 있는 오류를 알고 있어야 한다.

3 빈혈이 발견되면 MCV RDW 망상적혈구수를 3. 빈혈이 발견되면 MCV, RDW, 망상적혈구수를

통해 빈혈의 원인을 추정한다.

4 범혈구감소증이나 백혈적혈모구증 심한 4. 범혈구감소증이나 백혈적혈모구증, 심한

혈구 증가증, 원인을 알 수 없는 빈혈, 거대

적혈구성 빈혈이 발견된 경우에는 골수검사를 시행해야 한다.

시행해야 한다.

참조

관련 문서

Kawasaki disease (KD) is an acute febrile systemic vasculitis found predominantly in infants and young children. 1) The cause of KD remains unknown, but certain epidemiologic

The iron acquisition genes encoded expected functions such as low and high affinity iron permeases/ferroxidases, ferric reductases, and siderophore iron transporters (e.g.,

In addition, phosphorus values in serum, bones, wool, and teeth from affected Qianbei-Pockmarked goats were sig- nificantly lower, while serum AKP values were markedly

the realization of two-dimensional optical wavelength demultiplexers and multiports for surface plasmons polaritons (SPPs) based on plasmonic crystals, i.e., photonic

with iron deficiency anaemia and subnormal growth at puberty. The relationship between Helicobacter pylori infection and iron deficiency: seropreva- lence study in

Citrin deficiency is associated with two clinical phenotype; neonatal- onset type II citrullinemia (CTLN2), also known as neonatal intraphepatic cholestasis

2 School of Genomic Engineering, Hankyong National University, Anseong, Korea Wiskott-Aldrich syndrome, an X-linked immuno-deficiency disorder caused by

Abbreviations: AOSD = adult-onset Still’s disease, AUC = area under the curve, CBC = complete blood count, CRP = C-reactive protein, DAS28 = twenty-eight-joint Disease