Anaemia Flashcards

1
Q

50 year old man presents with lethargy and fatigue

What causes would you consider?

A

Psychological

Environmental

Endocrine

Haematological

Rheumatological

CV

Respiratory

Pharmacological

Dietary

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2
Q

50 year old man, increasing fatigue and lethargy for 6/12

Stable weight, no regular exercise, exertional dyspnoea and palpitations, no chest pain or tightness, recent constipation and 1 episode PR bleeding, no urinary symptoms, no cough, no sputum or haemoptysis, aches and pains in large joints and back, no rash

Non-drinker, smoker (15/day and a pipe)

FHx: thalassaemia

Rx: coloxyl, occasional voltaren

SHx: works full time shift work tyre factory, lives with fellow worker, migrated from Iraq 2 years prior, wife and 2 children remain in Iraq awaiting visas, previously worked as financial consultant

O/E: slim, BP 140/75, PR 100 bpm regular, pale, clear lung fields, normal HS tachycardic, abdomen soft, no hepatosplenomegaly, no masses palpable on abdomen, PR NAD

Ix?

A

FBE

UEC

LFTs

Iron studies

Thyroid function

ECG

CXR

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3
Q

50 year old man, increasing fatigue and lethargy for 6/12

Ix: FBE demonstrates Hb 102g/L with normal WCC and Pl 480, all others normal

Possible causes classified by pathophysiology?

A

Blood loss: GIT, menstrual, genitourinary, chronic recurrent epistaxis, hereditary AVM

Decreased production: anaemia of chronic disease (CKD, rheumatological disorders, malignancy), bone marrow infiltration, endocrine (hypothyroidism, EPO deficiency), nutritional deficiency (B12, folate, iron), infectious causes

Increased destruction: haemolysis, sequestration in spleen

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4
Q

Symptoms of chronic anaemia

A

Decreased O2 delivery:

Exertional dyspnoea

Fatigue

Signs and symptoms of hyperdynamic circulation including bounding pulses and palpitations (worsening symptoms if underlying heart or lung disease)

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5
Q

Symptoms which may point to an underlying cause of anaemia

A

Blood loss: haematemesis, malaena, change in bowel habit, tenesmus, PR bleeding, LOW, menstrual Hx

Chronic disease or inflammation: RA, chronic infection, renal failure, thyroid disease

Dietary: vegan, vegetarian, coeliac, parasitic infection

Bone marrow failure: bleeding, infection, fevers, sweats, LOW, Hx of radiotherapy, prior malignancy

Increased destruction: dark urine, jaundice, gall stones, FHx of splenectomy, cholecystectomy

Malabsorption

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6
Q

Patient’s blood results demonstrate MCV 78, MCHC low

Blood film shows hypochromic microcytic red cells, increased platelet and pencil cells

What are some causes of microcytic anaemia?

A

Anaemia of chronic disease (normal ferritin)

Haemoglobinopathy (normal ferritin)

IDA (decreased ferritin)

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7
Q

What malignancies can cause decreased RBC production and therefore anaemia?

A

Primary bone marrow malignancy: leukaemia, lymphoma, myeloma, myeloproliferative, myelodysplastic syndromes

Secondary malignancies: breast, prostate, melanoma

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8
Q

What infections can cause decreased production of RBCs and therefore anaemia?

A

Bacterial: TB, chronic suppurative disease

Viral: HIV, HCV, CMV, EBV, parvovirus

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9
Q

What does a normocytic anaemia with high reticulocyte count suggest about the underlying aetiology?

A

Haemolysis

Blood loss

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10
Q

What does a normocytic anaemia with normal/low (normal would be inappropriately low) reticulocyte count suggest about the underlying aetiology?

A

Anaemia of chronic disease

Renal failure

Marrow failure

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11
Q

What are the most common causes of anaemia in the elderly?

A

Nutrient deficiency (e.g. IDA)

CKD and/or AKI

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12
Q

What are the parameters for microcytic anaemia? How does microcytic anaemia arise on a molecular level?

A

MCV <80

Reduced iron availability causes reduced heme synthesis and globin production

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13
Q

What pathological processes may result in reduced iron availability and therefore a microcytic anaemia?

A

Iron deficiency due to deficient diet, malabsorption, increased requirements or increased loss

Anaemia of chronic disease (causes poor utilisation of iron; e.g. in chronic infection, inflammation, cancer liver disease)

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14
Q

What finding is seen on peripheral smear when haem synthesis is impaired?

A

Basophilic stippling

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15
Q

What pathological processes (besides reduced iron availability) can result in reduced haem synthesis?

A

Lead poisoning

Acquired or congenital sideroblastic anaemia

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16
Q

What pathological processes (besides reduced iron availability) can result in reduced globin production?

A

Thalassaemias

17
Q

What findings are seen on peripheral smear in thalassaemias?

A

Hypochromia

Microcytosis

Target cells

Tear drops

18
Q

Findings on iron studies:

Ferritin 15

Serum iron 2

Transferrin 3.0

Transferrin saturation 10%

What do each of these measures indicate and what is this clinical picture?

A

Ferritin: iron stores, low

Serum iron: iron supply (not a very reliable indicator), low

Transferrin: iron carrier molecule

TIBC: total iron binding capacity

Transferrin saturation: serum Fe/TIBC

Clinical picture consistent with IDA

19
Q

Differentiate between IDA, anaemia of chronic disease and thalassaemia in terms of expected results on iron studies parameters

A
20
Q

Explain normal iron metabolism

A

Dietary iron is carried by transferrin around the body and deposited in the liver for storage, or in the bone marrow and muscle for utilisation

Loss of iron occurs through sloughing of mucosal cells, desquamation, menstruation and other blood loss (including pathological)

21
Q

What are the clinical features of anaemia?

A

Fatigue

Pallor

Extertional dyspnoea

Koilonychia (spoon-shaped nails)

Angular cheilosis

Glossitis

22
Q

The patient reports change in bowel habit with PR bleeding, as well as lethargy; remember he is also a smoker

Ix?

A

FOBT

Gastroscopy

Colonoscopy (Ix of choice if symptomatic)

Tumour markers

23
Q

34 year old woman presents with jaundice, lethargy; previously well until flu-like illness 6/52, sore throat, 3/7 Hx of jaundice and no PMHx

Normal urine colour, no N+V, slight upper abdominal tenderness, no recent medications, bowels normal colour

No IVDU, high risk partners, transfusion Hx, overseas travel, joint pain, rash

FHx: sister with SLE, mother with hypothyroidism

Differential for jaundice and lethargy?

A
24
Q

34 year old woman presents with jaundice, lethargy; previously well until flu-like illness 6/52, sore throat, 3/7 Hx of jaundice and no PMHx

Normal urine colour, no N+V, slight upper abdominal tenderness, no recent medications, bowels normal colour

No IVDU, high risk partners, transfusion Hx, overseas travel, joint pain, rash

O/E: pale, jaundice, tachycardia, splenomegaly, no signs of CLD or infective endocarditis, no peripheral lymphadenopathy

Ix?

A

FBE

LFTs

UEC

Urinalysis

25
Q

Results of jaundiced patient’s bloods:

FBE: Hb 60, WCC 8.0, platelets 250, MCV normal

LFTs: bilirubin 70, AST and ALT marginally increased, normal GGT and ALP

UEC: normal

Urine: no proteinuria, haematuria

A
26
Q

Main causes of hypochromic microcytic, normochromic normocytic and macrocytic anaemias

A

Hypochromic microcytic: ISA, thalassaemia, sickle cell, lead poisoning, sideroblastic anaemia

Normocytic normochromic: anaemia of chronic disease, haemolysis, renal failure, pregnancy dilution

Macrocytic: B12 or folate deficiency, alcohol, liver disease, drugs, hypothyroidism, myeloma

27
Q

List 4 causes of immune-mediated acquired haemolytic anaemia

A

AI warm agglutinin

AI cold agglutinin

ADR

HDNB

28
Q

List 4 acquired causes of non-immune-mediated haemolytic anaemia

A

Malaria

Burns

Mechanical heart valve

Hypersplenism

PNH

29
Q

What are the causes of inherited haemolytic anaemia?

A

Abnormal RBC membrane: hereditary spherocytosis, hereditary elliptocytosis

Abnormal Hb: thalassaemia, sickle cell

Abnormal RBC metabolism: pyruvate kinase deficiency, G6PD deficiency

30
Q

Haemolysis screen

A

FBE and film

Reticulocyte count

Direct and indirect Coombs (antiglobulin)

LDH

Haptoglobin

Unconjugated bilirubin

Consider urinary and plasma Hb, urinary haemosiderin

31
Q

Results of patient’s haemolytic screen were as follows:

Elevated LDH

Elevated unconjugated bilirubin

Reduced haptoglobin

Blood film: spherocytes, bite cells, fragments, nucleated red cells, polychromasia

Direct Coombs test: Ig on surface of red cells

Urinary free Hb

Plasma free Hb

Is this an intravascular or extravacular haemolytic anaemia? How can you tell?

A

Intravascular

Features of intravascular haemolysis: blood film fragmentation, haemoglobinuria, haemoglobinaemia, haemosidinuria

32
Q

List 8 causes of intravascular haemolysis

A

DIC

Sepsis

Cardiac valvular disease

PNH

Extracorporeal circulation

TTP/HUS

Disseminated malignancy

AVM

33
Q

What Abs are responsible for cold and warm agglutinin respectively?

A

Cold: IgM

Warm: IgG

34
Q

List 3 pathologies which can induce cold agglutinin haemolytic anaemia

A

EBV

Mycoplasma pneumonia

Lymphoma

35
Q

List 5 pathologies which can induce a warm agglutinin haemolytic anaemia

A

Drug-induced

Lymphoproliferative disorder

SLE RA

Idiopathic AI haemolytic anaemia

Transfusion reaction

36
Q

How is haemolytic anaemia treated?

A

Corticosteroids

IVIG

Immunosuppression

Rituximab (anti-CD 20 monoclonal Ab)

Splenectomy

Dapsone

Anabolic steroids