️Type :
1. ALL
2. AML
3. JMML - juvenile myelomonocytic leukemia (rare)
❤What poor prognostic factor leukemia
- Male poorer
- Total White > 50
- Age ; less than 2 year
- Phidalephia chromosome (in JCML)
- Hypodiploid Karyotype (such as in Turner Syndrome) -if hyperploid like Klinefelter/Down Syndrome good prognosis
- More than 10@12 year old
- CNS involvement
- Splenomegally
- Hepatosplenomegally
- Bone marrow karyotype (percent blast cell)
- Response to first chemotherapy
-Mediastinum mass
❤️Significant side effect chemo? - but rate of occurance rare
- Tumor Lysis syndrome
(hyperkalemia, hypocalcemia, hyperphosphatemia, hyperuraemia - lead to Arrythmia / Kidney injury )
- Leukoencephalopathy (white matter disease)
- Night blindness
- Reduce hearing (bleomycin)
- Pulmonary fibrosis
- Cardiac : dilated cardiomyopathy, arrythmia, bradycardia
- Peripheral Neuropathy
- GIT : Antropathy
- Renal Toxicity
- Infertility
‼️Urgent Referal
- SVC obstruction
- Mediastinal mass
- SIADH
- Tumor Compression Effect (spinal compression effect need urgent referal)
- Febrile Neutropenia (late give antibiotic can cause death to patient)
🌸Mediastinal widening - leukaemia
SVC obstruction - Lymphoma
🌸Prognostic ALL
- Bone Marrow Karyotype
🌸Tumor Lysis syndrome mx?
- Hyperhydration
- Do not add pottasium, do not tranfuse blood cell except indicated, give hyperhyration
🌸Drug to prevent urate nephropathy
- Rasburicase / previously allopurinol
🌸Iron Chelation agent.
Eg : Desferal/ DFP/ Etc
Need to give Vit C to increase iron absorbtion.
8. Why patient thallasemia will have hyperpigmented skin?
🌸Because hemosiderin deposition in subcutaneous tissue.
9. How you monitor iron overload? Any blood parameter we can see?
🌸Serum Feritin level.
10. At what level of serum ferritin that we need to give iron chelation agent?
🌸If more than 1000 mcg/L
11. How we give desferal, by what route? For how long?
🌸SC/ IV
Eg : DFO : sc infusion 8-12 hours for 5 nights per week.
(Boleh double check Thallasemia Protocol Malaysia)
Tiada ulasan:
Catat Ulasan