Transcript
Page 1: Haem13 hemolytic anemia - acquired

Never say No, never say, ‘I cannot’, for

you are infinite. Even time and space

are as nothing compared with your

nature. You can do anything and

everything.

-- Swami Vivekananda

Page 2: Haem13 hemolytic anemia - acquired

….. foundation of clinical medicine

Shashidhar Venkatesh MurthyA/Prof & Head of Pathology

College of Medicine & Dentistry

Clinical Pathology:

RBC 1.3: Hemolytic Anemia - Acquired

CPC : Term2 Week1 - Haem 1/2.

System : Haematology - RBC Disorders.

Topic : 1: Anemia Intro 2: IDA, MBA & ACD 3: Acquired HA 4: Congenital HA. 5: Others.

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Pathogenetic Classification of Anemia:

Decreased Production:

Nutrient Deficiency.

Iron def (IDA) / Megaloblastic (MBA)

Hemopoietic cell defect:

Anemia of chronic disorders (ACD)

Aplastic anemia (AA).

Dysplastic anemia. Myelodysplastic Syndromes

Increased loss / destruction:

Blood loss anemia – Acute / Chronic - bleeding.

Hemolytic anemia – Congenital / Acquired.

Acquired / External injury.

Immune AIHA (Warm/Cold) Mechanical, Drugs & Parasites

Congenital / Internal RBC defect Defective Membrane (Spherocytic an)

Defective Hemoglobin (Sickle cell an.)

Deficient Enzyme (G6PD)3

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Top 6 Anemias:

1. Iron Def. A

2. Megaloblastic

3. Anem. Of Chronic Dis.

4. Aplastic An.

5. Immune Hemolytic – Warm

6. Immune Hemolytic - Cold

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Haemolytic Anemia: Introduction

Anemia due to Increased RBC destruction

life span (<120d) - Abnormal forms

Bilirubin Jaundice (Unconjugated)

RBC production – BM Hyperplasia &

Reticulocytes.

Acute: Pallor, Jaundice (normal urine)

Chronic: Splenomegaly, pigment gall stones.

Intravascular & Extravascular Hemolysis*.

Jaundice

2. Jaundice

4. Splenomegaly

3. Pigment Gall stones

1. Pallor

Immune

Mech.

Infection

Porphyrin Bil. Unconj

Globins

Iron

Bil. ConjConjugation

Normal

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Intravascular Hemolysis.

Etiology:

Immune, Mechanical, Enzyme def.

transfusion mismatch, drugs,

infections.

Lab diagnosis:

Absent Haptoglobins.

Haemoglobinemia

Haemoglobinuria

Haemosiderinuria

Clinical features:

Shock,

Renal failure,

In Extravascular Hemolysis:

Unconjugated hyperbilirubinemia only* 5

Breakdown of RBC within Blood Vessel

Renal

failure

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FBC Result: Hemolytic Anemia.

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Page 7: Haem13 hemolytic anemia - acquired

Hemolytic anemia: Morphology

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Abnormal RBC shapesspherocytes in WIHA, target forms

in thalasssemia etc.

Polychromatophils.(Immature RBC - large, bluish, no

central palor - Reticulocytes)

Nucleated RBCsmall nucleus inside reticulocyte.

ThalassemiaWarm Ab Hemolytic Anemia

Giems stain (routine blood film) Bluish, Large RBC ( MCV)

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Hemolytic Anemia: Reticulocytes

Reticulocyte

RBC

Reticulocytosis Increased RBC production

Methylene blue stain

for cytoplasmic RNA

Giemsa stain (routine blood film) Bluish, Large RBC ( MCV)

Page 9: Haem13 hemolytic anemia - acquired

Only educated person is

one who has learned how

to learn and change.

-- Carl Rogers

Page 10: Haem13 hemolytic anemia - acquired

Cell Mem

Hb

Enzymes

Haemolytic Anemia: classification

Acquired / External Injury:

Immune: IgG / Warm & IgM / Cold

Physical: valve dis, March Hb.nuria, trauma, burns.

Drugs: α-Methyldopa, cephalosporins, ibuprofen etc.

Parasites / infections (malaria, septicemia (DIC)

Congenital / Internal defects: Defective Membrane: Spherocytic anemia.

Defective Haemoglobin: Sickle cell anemia, Thalassemia

Deficient Enzyme: G6PD deficiency anemia.

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Immune Hemolytic anemia IgG/IgM:

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Causes:

RBC Antibody (Commonest.)

Pathogenesis:

Warm / IgG coated RBC lysis in spleen. Drugs,

Idiopathic. (predominantly extravascular)

Cold / IgM - (Infections, Lymphoma) RBC

Clumping & complement fixation lysis in BV &

Liver. (predominantly intravascular)

Morphology:

Spherocytes (warm) / RBC clumps (cold).

Clinical Features:

Anemia, Jaundice. Splenomegaly in chronic.

Diagnosis: Comb’s test *.

IgG

WARM

IgM

COLD

WARM / IgG

COLD / IgM

IgG Antibody

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AIHA: Lab diagnosis – Coombs test.

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Direct Coombs Test:

(for antigen on patient RBC)

Indirect Coombs Test:

(for antibodies in the serum.)Pos

Neg

Online Video Tutorial

Patient RBC Patient Serum

Page 13: Haem13 hemolytic anemia - acquired

MAHA - Microangiopathic Hemolytic An.

Mechanical damage:

Etiology:

DIC, TTP, HUS

Valve disease / Artificial valves.

March Hemoglobinuria.

Morphology:

Fragmented RBC: Schistocytes.

Polychromasia – reticulocytes.

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The only person who never makes

a mistake is a person who

never does anything…!

- Theodore Roosevelt

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Need help? contact me…

1. Office location: DB39-136 (Townsville)

2. Office Tel: 4781 4566

3. Email: [email protected]

4. Emergency?: 0416933704

Need personal coaching?Email me for an appointment.

You are the stone..

Page 16: Haem13 hemolytic anemia - acquired

The pessimist waits for better times,

and expects to keep on waiting; the

optimist goes to work with the best

that is at hand now, and proceeds to

create better times.

-- Christian D. Larson


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