Anemia Of Chronic Diseases Flashcards

1
Q

What is haemolysis?

A

The breakdown of red blood cells, which can lead to anaemia.

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2
Q

What common form of autoimmune haemolytic anaemia is associated with Chronic lymphocytic leukemia (CLL)?

A

Warm autoimmune haemolytic anaemia (AIHA)

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3
Q

What is a less common form of autoimmune haemolytic anaemia and its associated conditions?

A

Cold autoimmune haemolytic anaemia, found in Myeloma, lymphoplasmacytic lymphoma, and chronic cold agglutinin disease.

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4
Q

What type of anaemia may occur in association with disseminated carcinoma?

A

Microangiopathic haemolytic anaemia (MAHA) with intravascular haemolysis.

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5
Q

What chemotherapeutic agents are implicated in a syndrome resembling MAHA?

A
  • Mitomycin
  • Cisplatin
  • Bleomycin
  • Ciclosporin
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6
Q

What conditions lead to alcoholism-related anaemia?

A

Malnutrition and folate deficiency.

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7
Q

What are the morphologic abnormalities seen in alcoholism-related anaemia?

A
  • Dimorphic anaemia in peripheral blood film
  • Megaloblastic erythropoiesis
  • Vacuolation of erythroblasts
  • Ringed sideroblasts in bone marrow.
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8
Q

What are the clinical manifestations of lead poisoning?

A

Abdominal colic and motor neuropathy.

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9
Q

What type of anaemia is usually seen in lead poisoning?

A

Mild to moderate microcytic hypochromic anaemia.

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10
Q

What causes basophilic stippling in lead poisoning?

A

Aggregation of ribosomes within red blood cells due to lead-induced deficiency of Pyrimidine 5’ nucleotidase.

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11
Q

What findings in bone marrow are indicative of lead poisoning?

A

Erythroid predominance and ringed sideroblasts.

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12
Q

What is the mechanism of anaemia in lead poisoning?

A

Lead inhibits Aminolevulinic acid synthase (ALA), ALA dehydratase, and Ferrochelatase.

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13
Q

What laboratory findings are associated with lead poisoning?

A
  • Increased Serum Iron
  • Reduced TIBC (Total iron binding capacity)
  • Increased RDW (red cell distribution width)
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14
Q

What is the most frequent haematological abnormality found in patients with malignancy?

A

Anaemia.

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15
Q

What factors can worsen anaemia in cancer patients?

A

Myelotoxic effects of chemotherapy.

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16
Q

What is the response of plasma Epo levels in patients with malignancy-related anaemia?

A

Plasma Epo levels tend to be inappropriately low but respond well to Epo therapy.

17
Q

What conditions are associated with secondary acquired sideroblastic anaemia?

A
  • Myeloproliferative disorders
  • Multiple Myeloma (MM)
  • Acute Myeloblastic leukemia (AML) M6 subtype
  • Isoniazid, Pyrazinamide, Cycloserine, Chloramphenicol
  • Alcoholism
  • Lead poisoning
  • Vitamin B6 deficiency
18
Q

What characterizes primary acquired sideroblastic anaemia?

A

Refractory anaemia with ringed sideroblasts, typically found in myelodysplastic syndrome (MDS).

19
Q

What morphological abnormalities are seen in neutrophils in sideroblastic anaemia?

A
  • Pelger-Huet cells (neutrophils with double-lobed nucleus)
  • Hypogranularity.
20
Q

What is the pathogenesis of sideroblastic anaemia?

A

Haem synthesis is majorly affected.

21
Q

What are the types of sideroblastic anaemia reported?

A
  • Hereditary
  • Secondary acquired.
22
Q

What are the characteristics of hereditary sideroblastic anaemia?

A
  • X-linked disorder
  • Reduced activity of Delta aminolevulinic acid (δ-ALA) synthase
  • Presents in childhood or early adulthood with moderate to severe anaemia.
23
Q

What is red cell aplasia and where can it occur?

A

A condition where red blood cell production is severely reduced, found in Thymomas, CLL, NHL, and after chemotherapy/radiotherapy.

24
Q

What is the common feature of anaemia in chronic renal disease?

A

Reduced Epo production affecting erythropoiesis.

25
Q

What laboratory findings are indicative of anaemia of chronic renal disease?

A

Normocytic normochromic red cells and the presence of Burr cells (Echinocytes).

26
Q

What are sideroblasts?

A

Erythroblasts containing aggregates of iron, demonstrable by Prussian Blue reaction.

27
Q

What types of sideroblasts have been described?

A
  • Type I: Normal sideroblasts
  • Type II: Abnormal sideroblasts (numerous and large)
  • Type III: Ringed sideroblasts.
28
Q

What is the diagnosis criterion for ringed sideroblasts?

A

≥15% of these cells is diagnostic of sideroblastic anaemia.

29
Q

What characterizes laboratory findings in anaemia of chronic disease (ACD)?

A
  • Moderately reduced hemoglobin
  • Normal or mildly reduced MCV
  • Usually normal MCH
  • Reduced serum iron
  • Reduced TIBC
  • Mildly reduced transferrin saturation
  • Normal or increased serum ferritin
  • Raised serum and urine hepcidin.
30
Q

What cytokines are involved in the pathogenesis of anaemia of chronic disease?

A
  • IL-1
  • IL-6
  • TNF
  • Transforming growth factor (TGF-β).
31
Q

What are the causes of anaemia in malignancy?

A
  • Anaemia of chronic disease
  • Blood loss
  • Haemolysis (immune and non-immune)
  • Pure red cell aplasia
  • Megaloblastic anaemia
  • Marrow hypoplasia.
32
Q

What happens to Epo levels in anaemia of chronic disease compared to other types of anaemia?

A

Epo levels are inappropriately low.

33
Q

What is the role of hepcidin in iron metabolism during chronic disease?

A

Hepcidin binds to Ferroportin, inhibiting iron absorption and export from macrophages.