Blood Labs Flashcards

1
Q

Describe the lab findings and 3 basic causes of iron deficiency

Also, what are the other anemia’s associated with a low MCV?

A
  • Lab findings* Low MCV, low ferritin (unless inflammatory process), low serum Fe, high TIBC, low hemoglobin
  • Other anemia’s with low MCV*

ACD (would have low TIBC and high ferritin) , thal, lead poisoning, Hb E hemoglobinopathy, siderblastic anemia

Causes

Bleeding, malabsorption, intake

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2
Q

Autoimmune hemolytic anemia

  1. Etiology?
  2. Symptoms?
  3. Findings on CBC/smear?
A
  • Etiology*
  • In*fections, drugs, CLL, lymphomas, idiopathic, other autoimmune diseases (ex. SLE)
  • Symptoms*

The triad of hemolytic anemia - jaundice, anemia, and chronic splenomegaly

Findings on CBC/smear

Spherocytes, positive DAT, IgG positive, C3 positive

IF cold agglutination –> clumping of cells due to IgM, Rx is predisone or stay in warm temperatures (IgG neg, C3 pos)

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3
Q

Macrocytic anemia

  1. Etiology?
  2. Symptoms?
  3. Peripheral and lab tests findings
A

Etiology

Folate or B12 deficiency, hemolytic anemia - add other causes

Symptoms (thal on different cards)

General anemia symptoms –> neurological symptoms

Peripheral and Blood findings

High MMA/Homocysteine = B12, High homo only, could be folate

Hypersegmented neutrophils for folate and B12, macrocytic cells!

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4
Q

Name the diseases that causes MAHA and the findings on peripheral blood

A

Microangiopathic hemolytic anemia

Etiology

Thromcytic thrombocytopenia purpura (Ab to ADAMTS-13), hemolytic uremic syndrome (shiga toxin), disseminated intravascular coagulation (bleeding +/- thrombosis), extreme hypertension, HELLP

Smear findings

Helmet cells, schistocytes, polychromasia, low platelets

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5
Q

Sickle cell anemia

  1. Etiology
  2. Symptoms/Complications
  3. Tests and findings
  4. Treatment
A

Etiology

Autosomal recessive, two copies of Sickling hemoglobin gene –> HbS replaces all of the HbA. Heterzygotes are typically asymptomatic and resistant to malaria (but can show minor symptoms with very low oxygen or severe dehydration)

Symptoms

Various pain vaso-occulsive crises: acute chest syndrome, limb pain and abdo pain, dactilytis (sausage fingers due to inflam) and priapism (presistent painful erection)

Jaundice: hemolytic anemia (usually normocytic)

stroke: thrombi

infections from encapsulated organisms (N. menigititis, H. Influenza, Strep. Pneumo: patients usually have hyposplenism from repeated infarctions of spleen

Tests and findings

Howell jolly bodies and target cells (because of hyposplenism)

Sickle cells (under stress = metabolic acidosis, dehydration, and low O2 levels)

Hb electrophoresis or HPLC

Treatment

Avoid dehyration, O2 stress, acidosis

Hydroxerea to increase HbF

Exchange transfusion to give more HbA to replace HbS

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6
Q

Name two red cell membrane associated diseases and their findings on peripheral smear

A
  1. Hereditary elliptocytosis
    • Elliptocytes on the smear, symptoms range from mild to severe anemia requiring splenectomy
    • Anemia, splenomegaly and jaundice
  2. Hereditary Spherocytosis
    • Looks exactly like autoimmune hemolytic anemia, spherocytes (circular, no pallor) on the smear.
    • Also has a wide range of hemolytic anemia symptoms
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7
Q

Name the 4 reasons you would see reticulocytosis AND what that looks like on peripheral smear

A
  1. Bleeding
  2. Hemolysis
  3. Iron therapy
  4. Erythropoetin

You would see retics on smear (slighlty larger) and blue in color (polychromasia)

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8
Q

What causes basophilic stippling on a smear?

A

Lead poisoning

Basophilic stippling looks like little basophil granules on the periphery of an erythrocyte. It also causes a microcytic anemia. Treatment? Stop the lead!!!! Or chelation if severe. Diagnosis is serum lead.

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9
Q

Describe the clinical manifestations of malaria and the findings on the peripheral blood smear

A

Clinical

Anemia, rigors, jaundice, hemolytic anemia, fevers (cyclic shaking chills, sweating every 2 days)

Smear

See malarial organisms in the RBCs, stained small blue, sorta translucent like

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10
Q

List the findings on peripheral blood for someone with G6PD deficiency

A
  1. Heinz Bodies (denatured Hb on oxidative rxn –> looks like a blue dot on the actual periphery of an RBC
  2. Bite cells (macrophage has literaly taken a bite out of an RBC to remove the heinz body)

X-linked, shows up during oxidative stress. anti-malarials will cause the manifestations, so will other medications, fava beans, and infections

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11
Q

Alpha thalassemia findings on smear and genetics

A

Findings

HbH inclusions on RBCs

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