notes from quesmed Flashcards

1
Q

what are megaloblasts

A

large, oval shaped cells on blood film
abnormal, large and immature

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2
Q

when should prothrombin complex be administered

A

management of a raised INR in the presence of a major bleed. alongside iv vit k

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3
Q

macrocytic, megaloblastic anaemia

A

large red blood cells and immature redblood cell precursors
usually caused by impaired dna synthesis and abnormal maturation of red blood cells due to deficiencies in b12 or folate
think nutritional deficiencies, alcohol excess, pernicious anaemia

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4
Q

disseminated intravascular coagulopathy

A

haematological emergency
inappropriate activation of the clotting cascades, leading to thrombus formation (in microvasculature) and depletion of clotting factors and platelets, which then results in bleeding

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5
Q

bloods for DIC

A

thrombocytopenia
blood film may show shistocytes
raised D dimer
increased prothrombin time
increased APTT
decreased fibrinogen

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6
Q

polycythaemia rubra vera

A

increase in haematocrit, red cell count, haemoglobin concentration

spenomegaly

JAK2 mutation

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7
Q

how to tell hodgkins vs non hodgkins lymphoma

A

lymph node biopsy - reed sternberg cells present in hodgkins not non hodgkins
non hodkins more likely to associated with B symptoms

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8
Q

von willebrand disease

A

deficiency in vWF. also decreased factor VIII as vWF is necessary for stabilisation and transport of factor VIII
also normal PT time and prolonged APTT
increased risk of bleeding esp menstrual, pregnancy and childbirth

type 1 and type 2

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9
Q

type 1 VWD vs type 2

A

1- reduced quantity of vWF so increased bleeding often in adulthood
2- more severe as qualitative in vWF. presents earlier in life

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10
Q

myelofibrosis

A

myeloproliferative disorder with marrow fibrosis and pancytopenia

weight loss, fatigue, night sweats, splenomegaly, marrow failure, hepatomegaly, bone pain

poikilocytes (tear shaped RBCs)
platelet and WCC often high initially then pancytopenia
dry tap when aspirating due to fibrosis

JAK2 pos in 50% of cases

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11
Q

iron def and alcohol link

A

chronic liver disease, the liver cannot store or utilise iron properly, leading to decreased iron stores and eventual iron deficiency. Additionally, alcohol can impair iron absorption and cause gastrointestinal bleeding, further contributing to iron deficiency.

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12
Q

what is agranulocytosis

A

severe reduction in the number of granulocytes, a type of white blood cell, particularly neutrophils

absolute neutrophil count (ANC) of less than 0.5 × 10^9 per liter of blood.

increases risk of infections

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13
Q

drugs that cause thrombocytopenia

A

heparin, some antibiotics (penicillin), anti seizure meds, chemotherapy drugs

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14
Q

aplastic anaemia is

A

rare but serious medical condition characterized by a deficiency of all three major types of blood cells: red blood cells (erythrocytes), white blood cells (leukocytes), and platelets (thrombocytes). This deficiency occurs because the bone marrow fails to produce enough of these blood cells.

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15
Q

myelodysplastic syndrome (myelodysplasia)

A

group of blood disorders presenting with signs and symptoms of anaemia, infections and bleeding depending on which cell lineages are most affected. The anaemia can be normocytic or macrocytic and can be associated with single or multilineage dysplasia of other cells. Classic blood film findings are spur cells or acanthocytes and clusters of megakaryocytes.
blood film may show myeloblasts, but this should be less than 10% of the film.

The production of blast cells can be a risk factor for transformation to leukaemia.

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16
Q

cause of isolated thrombocytopenia

A

autoimmune

17
Q

symptoms of multiple myeloma

A

CRAB HAI

hyperCalcaemia
renal impairment
anaemia (other cytopenias can occur)
bone pain

hyperviscosity (headache, visual disturbance and thrombosis)
Amyloidosis
Infection - recurrent

18
Q

how to treat acute chest crisis in sickle cell

A

high-flow oxygen, antibiotics (with atypical cover) and exchange transfusion.

19
Q

management of polycythaemia rubra vera

A

regular venesection
aspirin 75mg daily

Cytoreductive therapy to suppress erythropoeisis in those where venesection isn’t sufficient, or those at high risk of thrombosis (most older patients):
1st line: hydroxycarbamide – suppresses erythrocytosis and causes a macrocytosis
2nd line: - Interferon, JAK-2 inhibitors (eg. ruxolitinib)
3rd line: Busulfan can be used but is leukaemogenic.
In younger patients, interferon is first line with hydroxycarbamide second line

also allopurinol and antihistamines, SSRIs or interferon for pruritis

20
Q

signs of haemolytic anaemia

A

increased lactate dehydrogenase (LDH), decreased haptoglobin, and elevated unconjugated bilirubin.
dark urine
jaundice
fatigue
gallstones

21
Q
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22
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22
Q
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