Non-Malignant Morphology Flashcards
Dhole Body
Blueish inclusion
Remanants of RER
Seen with inflammations, GCSF
Not in all neutrophils
May Hegglin Anomoly
Dhole bodies in all neutrophils
Macrothrombocytopenia
MYH9
Epstein syndrome, Fechtner syndrome
Chediak Higashi
AR disorder of lysosymal biogenesis CHS/LYST gene
large azurophilic granules in neutrophils and lymphocytes +MPO
Immunodef and oculocutaneous albinism, accelerated HLH
Pelger Huet Anomoly
bilobed nucleus of neutrophils in heterozygous mutations of laminin B
Homozygotes have unilobed nucelus
Still functional, all neutrophils will have if genetic, if stress will just be some
Alder-Reilly anomoly
prominent azurophilic granulation of all leukocytes due to lysosomal buildup of mucopolysaccharide (nml RBCs and plts)
Bordatella Pertusis
Lymphocytes with clefted nucelus
Lysosomal storage disorder
vacuolated lymphocytes
mucopolysaccharidosis, galactosialidosis, mucolipidosis, GM1 gangliosidosis
Beta Thalassemia
Basophilic stippling evenly distributed
Sideroblastic anemia
basophilic stippling more clumped and papenheimer bodies
ringed sideroblasts = iron granules surrounding nucleus
x-linked sideroblastic anemia from ALAS2
G6PD
heinz bodies (precipitated oxidized hemoglobin), blister cells
Stomatocytosis
mutation of RHAG gene overhydrated cells, increased osmotic fragility, low MCHC
Howell Jolly Bodies
Nuclear remnants
Splenectomy
severe hemolytic anemia
megaloblastic anemia
CDA
premature infants
Basophilic stippling
aggregated ribosomes
lead poisoning
thalassemia
Pyrimidine 5’nucleotidase deficiency
hemoglobinopathy
MDS
CDA
Pappenheimer bodies
lysosymes containing iron complexes
irregular clusters
Asplenia
iron overload
thalassemia
hemolytic anemia
CDA
sideroblastic anemia
hemoglobinopathies
Heinz bodies
denatured hemoglobin
G6PD
oxidative drug
homozygous hemoglobinopathies