Haematology & Oncology Flashcards

1
Q

Causes of iron deficiency

A

Poor intake
Malabsorption
Blood loss

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2
Q

Anaemia range

A

Neonate <140
>12 mnth <100
1-12<110

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3
Q

Main forms of sickle cell

A

HbSS-Homozygous for HbS - SIckle cell
HbSC
Sickle cell b-thalassaemia

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4
Q

Brain tumours in children

A

Astrocytoma (~40%) – varies from benign to highly malignant (glioblastoma multiforme).
• Medulloblastoma (~20%) – arises in the midline of the posterior fossa. May seed through the CNS via the CSF and up to 20% have spinal metastases at diagnosis.
• Ependymoma (~8%) – mostly in posterior fossa where it behaves like medulloblastoma.
• Brainstem glioma (6%) – malignant tumours associated with a very poor prognosis.
• Craniopharyngioma (4%) – a developmental tumour arising from the squamous remnant of Rathke pouch. It is not truly malignant but is locally invasive and grows slowly in the suprasellar region.
• Atypical teratoid/rhabdoid tumour – a rare type of aggressive tumour that most commonly occurs in young children.

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5
Q

Hodgkin Lymphoma clinical features

A

Painless lymphdenopathy

Symptoms are for months and can be systemic

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6
Q

Tx of hodgkin lymphoma

A

Chemotherapy with or without radiotherapy

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7
Q

Non hodgkin lymphoma clinical features

A

Presents like hodgkin or all

May have mediastinal mass or intestinal obstruction if abdomen involved.

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8
Q

Neuroblastoma clinical features

A

Abdominal mass
Over 2 years symptoms like metastatic diseases
ie. bone pain, bone marrow suppression causing weight pain and malaise

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9
Q

Wilms Tumour CF

A

Nephroblastoma w/ abdominal mass before 5 years

Haematuria

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10
Q

Haemophilia

A

A bleeding disorder, usually inherited, characterised by the deficiency of coagulation factor VIII or IX.

Occurs almost exclusively in males due to an X-linked pattern of inheritance.

Graded as mild, moderate, or severe, based on factor VIII or IX level.

Musculoskeletal bleeding is the most common type of haemorrhage.

Treatment consists of coagulation factor VIII or IX replacement.

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11
Q

Haemophilia A vs B

A

Factor VIII (A), Factor IX (B)

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12
Q

Tx of Haemophilia

A

A- Recombinant FVIII
B-Recombinant FVIX
For whenever there is a bleed

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13
Q

Complications of haemophilia

A

Reduce or inhibit effect of tx due to Ab treatment

Risk of infection: HIV, Hep A,B,C, Prions

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14
Q

Von Willebrand disease CF

A

Bruising
Excessive bleeding after surgery
Mucosal bleeding such as epistaxis and menorrhagia

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15
Q

vWD treatment

A

Type 1 -DDVAP (caution for under 1 risk of hyponatraemia and water retention)
More severe types of vWD have to be treated with plasma-derived FVIII concentrate

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16
Q

Thrombocytopenia

A

Platelet count <150
Mild 50-150
Moderate 20-50
Severe <20

17
Q

ITP

A

Most common cause of thrombocytopenia in children (Aged 2-10 years). Diagnosis of exclusion

18
Q

Febrile neutropenia

A

Febrile neutropenia is defined as a fever >38°C (>101°F) for 1 hour, with neutrophil less than 1x10*9

19
Q

common people to have febrile neutropenia

A

Children who have had chemotherapy for malignancy