Cancer Flashcards
Myelodysplastic Syndrome Patho
Exp to Chemo/RadioTx => BM fail + clonal expansion of Abnormal cells
MDS Features
Cytopenia, Hypercellular BM, Abnormal blast cells
If BM myeloblasts > 20% (WHO) or > 30% (FAB) => Acute Myeloid Leukaemia
MDS Mx
EPO,
G-CSF (Granulocyte Colony Stim Factor) Inj,
Blood Transfusions (w/ Iron Chelation),
BM Transplant
PV, ET Types of ?
Chronic Myeloproliferative Diseases
PV Signs, Sx
Hyperviscosity
(Headaches, Visual disturbances, Tinnitus, Thrombosis – Stroke, PE/DVT)
Pruritus (Histamine release)
Erythromelalgia (Sudden, severe burning in Hands + Feet w/ Inflamm)
PV Ix
(+) JAK2,
FBC (Raised RBC’s, Hb, Hct, WCC + Plt’s),
Low EPO,
BM Biopsy (Hypercellular)
PV Mx
Aspirin 75mg OD (Aim for Hct < 0.45: Reduce risk of VTE)
If Young: Venesection, If Old: Hydroxycarbamide
ET Signs, Sx
Thrombosis,
Easy Bleeding/Bruising (esp from Mucous Memb),
Erythromelalgia
Def Erythromelalgia
Sudden, severe burning in Hands + Feet w/ Inflamm
ET Ix
50% (+) JAK2,
FBC (Raised Plt’s: > 600),
BM Biopsy (Excess Megakaryocytes)
ET Mx
If Plt’s: 400-1000: Aspirin 75mg OD
If Plt’s > 1000/Thrombosis: Hydroxycarbamide
(Anagralide: Inhib Plt maturation => Reduce PC)
Def PV, ET
Polycythaemia Vera: (Excess Abnormal RBC’s):
Essential Thrombocytopenia: (Excess Abnormal Plt’s):
Primary Myelofibrosis Patho
Clonal proliferation of Megakaryocytes => Increase in Plt-derived GF (PDGF)
Replacement of Haematopoietic Tissue w/in BM w/ CT (via Collagen Fibrosis)
Primary Myelofibrosis Signs, Sx
Extramedullary Haematopoiesis (=> Hepatosplenomegaly), Hypermetabolism (Fever, Night Sweats, Weight loss), BM Fail (Pancytopenia)
Primary Myelofibrosis Ix
50% (+) JAK2,
FBC (Pancytopenia),
Blood film (Immature Blast cells, Teardrop Poikilocytes),
BM Biopsy (Hypercellular -> Hypocellular w/ marked Fibrosis: Dry Tap)
Primary Myelofibrosis Mx
Replacement RBC’s/Plt’s + Immunoglobulins
Splenectomy
Allogenic BM Transplant
ALL Def, Eped, Patho
Acute Lymphoblastic Leukaemia (ALL):
(M Comm Child Cancer, Peak: 2-5yo):
Arrest of maturation + proliferation of Lymphoblasts (=> B + T cells) => BM Fail
ALL Sx
Severe/Recurrent/Atypical Inf,
Anaemia, Thrombocytopaenia
ALL Ix
FBC (Normal/Raised WCC – esp Lymphoblasts, Low RBC’s/Plt’s/Neutrophils), BM Asp (> 20% Blasts)
ALL Mx
Replace blood products Allopurinol (Prevent Hyperuricaemia) Inf Prevention: Cotrimoxazole, Ciprofloxacin, Inf Tx: Gentamicin + Tazocin ChemoTx BM Transplant
AML Def, Eped, Patho
Acute Myeloid Leukamia (AML):
(Increased risk w/ Age):
Neoplastic proliferation of Myeloblasts => BM Fail
AML Ix
FBC (Low RBC/Plt, Normal/Raised WCC), BM Asp (> 20% Blasts, Auer Rods)
AML Mx
Replace blood products
Allopurinol (Prevent Hyperuricaemia)
Inf Prevention: Cotrimoxazole, Ciprofloxacin,
Inf Tx: Gentamicin + Tazocin
ChemoTx
BM Transplant
(Early: Autologous replacement, Late: Chemo + Total Body Irradiation => Destroy BM w/ Allogenic Replacement)
CLL Def, Eped, Patho
Chronic Lymphocytic Leukaemia (CLL):
(Older males, M Common Leukaemia):
Neoplasm of mature B-cells
CLL Sx
Asymptomatic
Symmetrical, Painless Lymphadenopathy (Gradually Obstruct),
Hepatosplenomegaly,
(+/- Evan Synd: Auto-Immune Haem Anaemia + ITP)
CLL Ix
FBC (Raised WCC – Lymphocytosis w/ Low serum Ig), Blood Film (Smudge Cells: Cells w/ Bact surrounding)
CLL Mx
Chemo: Fludarabine, Cyclophosphamide, Rituximab
RadioTx
(1/3 never progress, 1/3 progress w/ time, 1/3 Act progress => Large B-cell Lymphoma)
CML Def, Eped, Patho
Chronic Myeloid Leukaemia (CML):
Clonal proliferation of Myeloid cells (Reciprocal translocation btw Chromosomes 9 and 22 => BCR-ABL fusion gene => Increased Tyrosine Kinase Act)
CML Phases
Chronic Phase (< 5% blasts: Asymptomatic),
Accelerated Phase (10-20% blasts: Late-onset),
Blast Crisis/Acute Leukaemia (> 20% blasts: Inf, Anaemia, Bleeding/Bruising, Rapid-cell Turnover/Proliferation => Hypophosphataemia)
CML Ix
FBC (Raised WBC’s, If Accelerated/Blast Phase: Low Hb/Plt’s),
BM Asp w/ Cytogenic Analysis (Philadelphia +)
CML Mx
If Phil(+): Imatinib (Tyrosine Kinase Inhib)
If Phil(-)/Blast crisis: Allogenic SC Transplant
NHL Def, Sx
Non-Hodgkins Lymphoma: (80%):
Lymphadenopathy:
Symmetrical, Multiple Sites
Painless
Spreads discontiguously
NHL Ix
Raised LDH,
LN/BM Biopsy (Grading),
CT/MRI CAP (Staging)
NHL Mx
If Low grade: Chemo (Chlorambucil)
If High grade: R-CHOP21 (Rituximab, Cyclophosphamide, Doxorubicin HCl, Vincristine, Pred) given for 21 days
If relapse: BM Transplant
HL Def, Sx
Hodgkins Lymphoma: (20%, ass w/ EBV):
Lymphadenopathy:
Asymmetrical (M common: Cerv LN’s)
Painless (+/- Alc-induced Pain)
Spreads contiguously to Adjacent LN’s
(Pruritus, Pel-ebstein Fever: Cyclical Fever)
HL Ix
Low Hb,
Raised ESR,
LN Biopsy/FNA (Grading, Reed-sternberg Cells: Large, Multi-nucleated),
CT/MRI CAP (Staging)