Haem Onco Flashcards

(52 cards)

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
Different types of anemia and their etiology
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
Difference between Vitamin B12 and folate
Vit B12 is cobalamin Vit B9 is folate
27
Tests to dx Iron Deficiency Anemia(IDA)
?
28
Triad of hemolytic anemia
Pallor Jaundice Splenomegaly
29
Differentiating IDA and thalassemia
Mentzer Index: MCV/Hb >13 IDA <13 Thalassemia
30
What is IRIDA
Iron refractory Iron Deficiency Anemia Will probably require parenteral Iron
31
Inheritance of G6PD deficiency
X linked recessive, hence more common in boys
32
Triggers for hemolysis in G6PD deficiency
Sulphur containing drugs eg Cotrimoxazole Anti malarials eg chloroquine Stressors eg infection, inflammation, Acidosis Fava beans Moth balls
33
Gold standard for G6PD deficiency diagnosis
G6PD enzyme quantitative analysis
34
Predictors of ITP(Immune thrombocytopenic purpura)prognosis
Age more than 10 worse Chronic, moderate thrombocytopenia worse Gender, female worse
35
Gold standard to dx Hemophilia
Factor 8 or 9 Quantitative Assay
36
Severity of Hemophilia grading
Severe: <1% Moderate: 1-5% Mild: 5-40%
37
Electrolyte abnormalities caused by Tumour Lysis Syndrome
HypoK HypoCa Hyperphophatemia Hyperuricemia
38
What do are myelodysplastic syndromes at risk of progressing to
Acute myeloid leukemia
39
What are examples of myeloproliferative neoplasms
Primary Myelofibrosis Chronic Myeloid leukemia Polycythemia rubra vera Essential thrombocytosis
40
What are the etiologies of myelodysplastic syndromes
Primary idiopathic Secondary eg to radiation or drugs
41
What is contraindicated in Hemophiliac with hematuria
Tranexamic acid
42
Treatment of overwarfarinisation
Vitamin K FFP PCC(Prothrombin Complex concentrate)
43
Mnemonic for multiple myeloma clinical manifestations
CRAB Calcium high Renal impairment Anemia Bone disease
44
Types of malignancies that commonly cause tumor lysis syndrome
Hematological: lymphoma and leukemia and some solid organ tumors eg SC lung Ca
45
Electrolyte derangements in tumor lysis syndrome
Hyperkalemia, Hyperuricemia, Hyperphosphatemia and hypocalcemia
46
47
Salt and pepper appearance of bones on MRI
Multiple myeloma
48
Causes of massive splenomegaly
1. Myelofibrosis 2. Kala Azar 3. Tropical Malaria
49
Malignancy associated with Philadelphia chromosome
Acute lymphoblastic leukemia
50
Reversal agent for heparin
Protamine sulfate, binds and inactivates heparin
51
Common sites of bleeding in Hemophilia A and B
1. Haemarthrosis 2. Intracranial hemorrhage 3. Mucosal bleed: BGIT 4. Hematuria
52