HEMATOLOGY MNEMONICS

 AnemiaTIBC finding to differentiate iron deficiency vs. chronic disease

TIBC levels at the:

  • Top=Iron deficiency.
  • Bottom=Chronic disease.

Anemia causes (simplified)

ANEMIA:

  • Anemia of chronic disease
  • No folate or B12
  • Ethanol
  • Marrow failure & hemaglobinopathies
  • Iron deficient
  • Acute & chronic blood loss

Anemia (normocytic): causes

ABCD:

  • Acute blood loss
  • Bone marrow failure
  • Chronic disease
  • Destruction (hemolysis)

Anemianon-megaloblastic causes of macrocytic anemia

HAND LAMP:

  • Hypothyroidism
  • Aplastic anaemia
  • Neonates
  • Drugs
  • Liver disease
  • Alcohol
  • Myelodyplasia
  • Pregnancy

Blood disorderscommoner sex

  • HE (male) gets:
  • HEmophilia (X-linked)
  • HEinz bodies (G6PD deficiency, causing HEmolytic anemia: X-linked)
  • HEmochromatosis (male predominance)
  • HEart attacks (male predominance)
  • HEnoch-Schonlein purpura (male predominance)
  • SHE (female) gets:
  • SHEehan's syndrome

Haematologykey numbers

  • and are key in in haematology:
  • 1.34 cm3 of oxygen is carried by a gram of hemoglobin.
  • There's 3.4mg of iron in each gram of hemoglobin.
  • There's an average of 3.lobes per neutrophil.
  • There's 34mg bilirubin from each gram of hemoglobin

Hemoglobin and myoglobinbinding strengths, sites

"ABC" of glycosylated Hb (Hb1c):

  *Glucose binds to Amino terminal of Beta Chain.

"Hbbinds Forcefully":

  *HbF binds oxygen more forcefully than HbA, so Oxy-Hb dissociation curve shifts to left.

Stored blood is SOS:

  *Stored blood Hb binds to Oxygen Strongly because of decrease in 2,3 BPG.

2,3 BPG binding site is BBC:

  *BPG binds to Beta Chain of Hb.

Myoglobin binding strength is MOM:

  *Myoglobin binds Oxygen More strongly than Hb.

Hemolytic anemia: types

SHEEP TIT:

  • Sickle cell
  • Heriditary splenocytosis
  • Enzyme deficiencies: [G6P, pyruvate kinase]
  • Erythroblastosis fetalis
  • Paroxysmal nocturnal hemoglobinuria
  • Trauma to RBCs
  • Immunohemolytics: [warm Ab, cold Ag]
  • Thalassemias: [alpha, beta]

Hemophiliatype A factor

  • Hemophilia A: problems with VIII factor (number as an inverted A).

Hodgkin's lymphoma: classification

  • AAsymptomatic
  • BBad

Leukemiasacute vs. chronic rules of thumb

ABCDE

  • Acute is:
  • Blasts predominate
  • Children
  • Drastic course
  • Elderly
  • Few WBC's (so Fevers)

  *Chronic is all the opposites:

  • Mature cells predominate
  • Middle aged
  • Less debilitating course
  • Elevated WBC's, so not a history of fevers and infections

Macrocytic anemiacauses

ABCDEF:

  • Alcohol + liver disease
  • B12 deficiency
  • Compensatory reticulocytosis (blood loss and hemolysis)
  • Drug (cytotoxic and AZT)/ Dysplasia (marrow problems)
  • Endocrine (hypothyroidism)
  • Folate deficieny/ Fetus (pregnancy)

Macrocytic anaemiadifferential

FAT RBC:

  • Fetus (pregnancy)
  • Alcohol
  • Thyroid disease(ie hypothyroidism)
  • Reticulocytosis
  • B12 and folate deficiency
  • Cirrhosis and chronic liver disease

Marble bone diseasesigns and symptoms

MARBLES:

  • Multiple fractures
  • Anemia
  • Restricted cranial nerves
  • Blind & deaf
  • Liver enlarged
  • Erlenmeyer flask deformity
  • Splenomegaly

  *Eponymous name: Marbles Albers-Schonberg (anagram).

Megaloblastic anemiavitamin B12 deficiency vs. folate deficiency

  • Vitamin B12 deficiency also affects Brain (optic neuropathy, subacute combined degeneration, paresthesia).

  *Folate deficiency is not associated with neurological symptoms.

Microcytic anemia: causes

"Find Those Small Cells":

  • Fe deficiency
  • Thalassemia
  • Sideroblastic
  • Chronic disease

Pancytopaeniadifferential

"All OMBlood Has Taken Some Poison":

  • Aplastic anaemias
  • Overwhelming sepsis
  • Megaloblastic anaemias
  • Bone marrow infiltration
  • Hypersplenism
  • TB
  • SLE
  • Paroxysmal nocturnal haemoglobinuria

Polycythemia Rubra Vera (PRV): common symptoms

PRV:

  • Plethora/ Pruritis
  • Ringing in ears
  • Visual blurriness

Sickle cell diseasecomplications

SICKLE:

  • Strokes/ Swelling of hands and feet/ Spleen problems
  • Infections/ Infarctions
  • Crises (painful, sequestration, aplastic)/ Cholelithiasis/ Chest syndrome/ Chronic hemolysis/ Cardiac problems
  • Kidney disease
  • Liver disease/ Lung problems
  • Erection (priapism)/ Eye problems (retinopathy)

Symptoms of TTP/HUS

"Nasty Fever Ruined MTubes":

  • Neurological symptoms
  • Fever
  • Renal failure
  • Microangiopathic hemolytic anemia
  • Thrombocytopenia

Thrombotic thrombocytopenic purpurasigns

FAT RN:

  • Fever
  • Anemia
  • Thrombocytopenia
  • Renal problems
  • Neurologic dysfunction

TTPclinical features

Thrombosis and thrombocytopenia PARTNER together:

  • Platelet count low
  • Anemia (microangiopathic hemolytic)
  • Renal failure
  • Temperature rise
  • Neurological deficits
  • ER admission (as it is an emergency)

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