Haematological changes in systemic disease Donald mcdonald 250821 Flashcards
Primary disorders - germline inherited
FIX - deficiency = haemophilia B
excess = FIX padua
erthryocytes
deficiency = beta thalassaemia
excess = VHL gene = chuvash polycythaemia
Primary disorders - acquired
e.g. leukaemia
secondary disorders - erythrocytes
excess - cyanotic heart disease/hypoxia
deficiency - anti RBC antibodes - immune haemolysis
describe the causes and findings of iron deficiency and underlying malignancy
microcytic hypochromic anaemia reduced ferritin transferrin saturation raised TIBC
causes - blood loss e.g. gastric/renal cell cancer, maenorrhagia
describe what youd see on blood film in leuco erythroblastic anaemia?
teardrop RBCs, nucleated RBCs, immature myeloid cells
causes of leucoerythroblastic anaemia film
malignant (haemopoietic, non haemopaetic), severe infection (miliary TB, severe fungal infection), myelofibrosis (massive splenomegaly, dry tap on bM aspirate)
common features of haemolytic anaemias
anaemia, reticulocytosis, unconjugated bilirubin raised (pre-hebatic, LDH raised (intracellular contents of RBC), haptoglobins reduced,
Haemolytic anaemias can be divided into
inherited and acquired
inherited haemolytic anaemias
membrane (hereditary spherocytosis), cytoplasm (G6PD), Haemoglobin (SICKLE CELL)
acquired haemolytic anaemias
immune, non-immune
Immune mediated anaemia - DAT positive what will you see on blood film
spherocytes, agglutination, dat positive
non-immune mediated anaemia what will you see on blood film
RBC fragments (schistocytes)< thrombocytopenia, DAT negative
causes of non-immunemediated anaemia
infection (malaria),
paroxysmal nocturnal haemoglobinuria (hams test positive)
microangiopathic haemolytic anaemia (MAHA - adenocarcinoma, HUS, TTP)
female with breast cancer recent jaundice and hepatomegaly, low reticulocytes,dat negative, immature cells in blood film
leucoerythroblastic anaemia due to BM mets
causes of neutrophilia
corticosteroids, neoplasia, tissue inflammation (colitis or pancreatitis), myeloproliferative or leukemic disorders, pyogenic infection (most likely)
evaluating neutrophils - reactive infection
neutrophilia, toxic granulation, no immature cells, only neutrophils, heavy granulation, vacuoles in the neutrophils
evaluating neutrophils - malignant
neutrophilia, basophilia, immature cells (myelocytes)+ splenomegaly = CML
neutropenia +myeloblasts = AML
how does the kappa lambda ratio change in monoclonal b cell lymphocytosis
becomes mainly kappa, or mainly lambda- monoclonal
Lymphocytosis causes
EBV, CMV, infectious hepatitis, rubella, herpes, Autoimmune sarcoidosis
Eosinophilia causes
parasites, allergy, hodgkins, reaction erythema multiforme, chronic eosinophilic leukemia
chronic vs acute myeloid leukaemia
chronic - proliferation increased, differentiation normal
acute - proliferation increased and differentiation blocked
how is a leukaemia/lymphoma diagnosis establoshed
morphology ( large small, mature, immature) immunophenotype (myeloid, lymphoid, t or b lineage) , cytogenetics (chromosome translocations etc) , molecular genetics