Hematology Flashcards
DIC in sepsis
Deranged coagulation
Cryoprecipitate constitution
factor 8 + fibrinogen + vWF + factor 13
Hemoarthroses, hematomas, prolonged bleeding; prolonged APTT
Hemophilia Factor 8 and 9
Factor 5 leidin
Activated protein C resistance
Inherited thrombophilia commonest
Tear drop poikilocytes
Myelofibrosis
Pencil piokilocytes
iron deficiency anemia
Howell-Jolly Bodies and Siderocytes
hyposplenism
Schistocytes
Hemolysis Such as Hereditary spherocytosis
Spherocytes
Hereditary spherocytosis or AIHA
CML treatment
Imatinib- TK inhibitor
Ritcher’s transformation
B symptoms - fever, weight loss, nigh sweats; CLL to large cell lymphoma; diagnose by biopsy of lymph node
DIC on coagulation test
Low platelet
Low fibrinogen
Increased PT and APTT
Increased FDPs
VTE risk
Factor 5 Leiden or Protein C resistance
Bleeding disorder that is inherited autosomal
VWF
Anti Tb medication, alcohol, myelodysplasia, lead and microcytosis are related to
Sideroblastic anemia
Basophilic stippling of cells - RBC
Sideroblastic Anemia
Most common type of leukaemia in adults
Chronic Lymphocytic Leukemia
Blood film of CLL
Smear cells aka Smudge cells
Petichae, purpura, epistaxis, in old females
ITP
1st line management of ITP
Prednisolone
Band cells
CML
BLAST CELLS
AML
Burkitt’s Lymphoma mutation
C-MYC gene translocation
Clotting in Hemophilia - PT, APTT and Bleeding time
APTT increased
PT normal
BT normal
Coagulation test in VWD
APTT raised
PT normal
Bleeding time raised
Vitamin K deficiency coagulation
APTT increased
PT increased
Bleeding time normal
CLL to High grade non-Hodgkin lymphoma is called
Ritcher’s transformation
Tumour lysis syndrome
Lymphoma + Chemo + uremia, Hyperkalemia, hyperphosphatemia and hypocalcemia and increased creatinine/ Arrhythmia or seizure
Hypercalcemia; Pancytopenia and AKI, Proteinuria
Multiple myeloma
Myelodysplasia transforms into?
Acute myeloid Leukemia
Smudge cells or Smear cells
CLL
Pseudo-pelger Huet cells
CML
Back pain, >60, leukopenia and Hypercalcemia. choice of investigation
Protein electrophoresis and Bence-Jones protein testing
A painful maculopapular rash in a allogenic host
Graft vs Host disease
Isolated Low platelets
Commonly ITP
Anemia, Fever, purpura and cerebral dysfunction; a hematological disorder, low platelets, microangiopathic anemia, AKI
TTP
IgA deficiency increases the risk of blood transfusion reaction
Anaphylactic
EMA binding test is used for
Hereditary spherocytosis
Basophilic stippling and Cabot rings
Lead poisoning
Rouleaux formation
Myeloma
Lymphoma, Raynauld’s, worse on cold symptoms and new macrocytic anemia
AIHA
Ovarian cancer spreads
Locally
Myeloma - Calcium, Phosphate and ALP
High calcium
Normal or high phosphate
NOrmal ALP
Haemarthrosis is a sign of what hemotological disease
Hemophilia A
CLL is associated with what type of haemolytic anemia
Warm autoimmune anemia
COLD AIHA
Lymphoma, EBV, mycoplasma