Haem Onco Flashcards

1
Q

3 main cancers that are screened for

A

Breast,Cervical and Colorectal

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2
Q

How cancers can be prevented

A

HPV,EBV vaccination

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3
Q

Criteria for monitoring cancer treatment response

A

RACES for chemotherapy,modified RACES for chemotherapy

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4
Q

Uses of imaging in oncology

A

Diagnostic(biopsy), gauging response of cancer to treatment,planning treatment in terms of locations to target with treatment

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5
Q

Threshold for diagnosing Hypercalcemia

A

2.0mmol/L

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6
Q

Can we solely use Calcitonin for Long term treatment of HyperCalcemia

A

No as that will cause tachyphylaxis. For long term it is better to use Zoledronic acid(together with calcitonin)

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7
Q

Why is immobilisation important for radiotherapy

A

To ensure precision in the administration of radiation to the specific clinical and planning margins for the tumour

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8
Q

Primary uses for radiotherapy

A

Palliative,curative and as an adjunct

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9
Q

Indications of radiotherapy for palliative purposes

A
  1. Severe bone pain esp from metastasis
  2. Bleeding eg for haemoptysis for lung ca
  3. Obstruction eg for esophageal ca
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10
Q

MOA of radiotherapy

A

Radiotherapy mostly works by replicative failure(indirect cell kill),not direct cell kill

1st phase: Release cytokines to relieve pain
2nd phase: Cause thrombosis etc to reduce angiogenesis and bleeding
3rd phase: Mostly indirect cell kill

Take this slide with a pinch of salt

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11
Q

Why is LH-RH used for prostate and breast cancer

A

Gland(pituitary?) is first hyperstimulated which subsequently causes reduced hormone release causing reduced stimulation of the affected organ and subsequently reducing tumour growth

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12
Q

Preferred therapy for Haematological cancers and NPC respectively

A

Haemarological spreads even at early stages, chemo is important for systemic treatment for mets.

NPC in especially sensitive to radiotherapy

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13
Q

What is SVC syndrome

A

Caused by obstruction of blood flow through Superior Van Cava(Medical urgency). When collateral veins can’t compensate quickly enough or at max compensation

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14
Q

Pathophysiology of SVC syndrome

A

1)Thrombosis/Sclerosis
2)Invasion
3)Extrinsic pressure by pathology

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15
Q

Causes of SVC syndrome

A

Usually caused by malignancy(SCLC,NSCLC,NH lymphoma,metastatic disease. Less commonly benign lesions

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16
Q

Signs of SVC Syndrome

A

3 Ds: Dsypnea, Distension including upper body Edema, Dilated chest wall veins + Neurological symptoms due to cerebral edema

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17
Q

Investigations relevant to SVC syndrome

A

if no overt presentation of syndrome: Ultrasound if intravascular device, CT/MRI for Hx of malignancy, CXR to look for SVC obstruction,mediastinal widening, pleural effusion

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18
Q

Mgmt of SVC syndrome

A

Treatment: Relieve symptoms(Severe: Stent,radiotherapy,steroids vs Non severe: radio+/- Chemo)+ Treat primary malignancy

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19
Q

Pathophysiology of Spinal Cord Compression

A

Impingement of spinal cord by tumour whether primary or metastatic,is a medical emergency

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20
Q

Types of Spinal Cord Compression

A

Vertebral displacement, epidural compression and paraspinal compression

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21
Q

Common sources of metastasis causing Cord compression

A

Myeloma,NPC,prostate and breast

22
Q

Symptoms of Spinal Cord Syndrome

A

Back pain,motor and sensory dysfunction, bladder and Bowel dysfunction

23
Q

Mgmt of Spinal Cord Compression

A

Is a medical emergency to prevent irreversible neurological sequelae: Corticosteroids, Analgesia, radiotherapy or surgical decompression

24
Q

Ways hemophilia can present

A

Haemarthrosis(most specific)
Ecchymoses
Prolonged bleeds
Epistaxis
Melena/Hematochezia
Haematuria
Brain bleeds

25
Q

Different types of anemia and their etiology

A

Hypochromic Microcytic
1)Iron Deficiency
2)Thalassemia
3)Chronic disease/inflammation

Normocytic Normochromic
1)Blood loss
2)Hemolysis
3)Chronic disease and inflammation

Macrocytic
1)Folate deficiency
2) Vit B12 deficiency

Other cell lines affected: Suspect haematological malignancy or myelodysplastic syndrome

26
Q

Difference between Vitamin B12 and folate

A

Vit B12 is cobalamin
Vit B9 is folate

27
Q

Tests to dx Iron Deficiency Anemia(IDA)

A

?

28
Q

Triad of hemolytic anemia

A

Pallor
Jaundice
Splenomegaly

29
Q

Differentiating IDA and thalassemia

A

Mentzer Index: MCV/Hb

> 13 IDA
<13 Thalassemia

30
Q

What is IRIDA

A

Iron refractory Iron Deficiency Anemia

Will probably require parenteral Iron

31
Q

Inheritance of G6PD deficiency

A

X linked recessive, hence more common in boys

32
Q

Triggers for hemolysis in G6PD deficiency

A

Sulphur containing drugs eg Cotrimoxazole
Anti malarials eg chloroquine
Stressors eg infection, inflammation, Acidosis
Fava beans
Moth balls

33
Q

Gold standard for G6PD deficiency diagnosis

A

G6PD enzyme quantitative analysis

34
Q

Predictors of ITP(Immune thrombocytopenic purpura)prognosis

A

Age more than 10 worse
Chronic, moderate thrombocytopenia worse
Gender, female worse

35
Q

Gold standard to dx Hemophilia

A

Factor 8 or 9 Quantitative Assay

36
Q

Severity of Hemophilia grading

A

Severe: <1%
Moderate: 1-5%
Mild: 5-40%

37
Q

Electrolyte abnormalities caused by Tumour Lysis Syndrome

A

HypoK
HypoCa
Hyperphophatemia
Hyperuricemia

38
Q

What do are myelodysplastic syndromes at risk of progressing to

A

Acute myeloid leukemia

39
Q

What are examples of myeloproliferative neoplasms

A

Primary Myelofibrosis
Chronic Myeloid leukemia
Polycythemia rubra vera
Essential thrombocytosis

40
Q

What are the etiologies of myelodysplastic syndromes

A

Primary idiopathic

Secondary eg to radiation or drugs

41
Q

What is contraindicated in Hemophiliac with hematuria

A

Tranexamic acid

42
Q

Treatment of overwarfarinisation

A

Vitamin K
FFP
PCC(Prothrombin Complex concentrate)

43
Q

Mnemonic for multiple myeloma clinical manifestations

A

CRAB

Calcium high
Renal impairment
Anemia
Bone disease

44
Q

Types of malignancies that commonly cause tumor lysis syndrome

A

Hematological: lymphoma and leukemia and some solid organ tumors eg SC lung Ca

45
Q

Electrolyte derangements in tumor lysis syndrome

A

Hyperkalemia, Hyperuricemia, Hyperphosphatemia and hypocalcemia

46
Q
A
47
Q

Salt and pepper appearance of bones on MRI

A

Multiple myeloma

48
Q

Causes of massive splenomegaly

A
  1. Myelofibrosis
  2. Kala Azar
  3. Tropical Malaria
49
Q

Malignancy associated with Philadelphia chromosome

A

Acute lymphoblastic leukemia

50
Q

Reversal agent for heparin

A

Protamine sulfate, binds and inactivates heparin

51
Q

Common sites of bleeding in Hemophilia A and B

A
  1. Haemarthrosis
  2. Intracranial hemorrhage
  3. Mucosal bleed: BGIT
  4. Hematuria
52
Q
A