Haematology & Oncology Flashcards
Causes of iron deficiency
Poor intake
Malabsorption
Blood loss
Anaemia range
Neonate <140
>12 mnth <100
1-12<110
Main forms of sickle cell
HbSS-Homozygous for HbS - SIckle cell
HbSC
Sickle cell b-thalassaemia
Brain tumours in children
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.
Hodgkin Lymphoma clinical features
Painless lymphdenopathy
Symptoms are for months and can be systemic
Tx of hodgkin lymphoma
Chemotherapy with or without radiotherapy
Non hodgkin lymphoma clinical features
Presents like hodgkin or all
May have mediastinal mass or intestinal obstruction if abdomen involved.
Neuroblastoma clinical features
Abdominal mass
Over 2 years symptoms like metastatic diseases
ie. bone pain, bone marrow suppression causing weight pain and malaise
Wilms Tumour CF
Nephroblastoma w/ abdominal mass before 5 years
Haematuria
Haemophilia
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.
Haemophilia A vs B
Factor VIII (A), Factor IX (B)
Tx of Haemophilia
A- Recombinant FVIII
B-Recombinant FVIX
For whenever there is a bleed
Complications of haemophilia
Reduce or inhibit effect of tx due to Ab treatment
Risk of infection: HIV, Hep A,B,C, Prions
Von Willebrand disease CF
Bruising
Excessive bleeding after surgery
Mucosal bleeding such as epistaxis and menorrhagia
vWD treatment
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