🩸🥶 Anemias For The ASCP
Hello My Little Hang of Nasties 😜😈
If you are in need of a solid review of the major anemias, this resource covers the essentials; from pathophysiology to lab findings and morphology under the microscope. See below or click the .pdf attachment.
Here’s a breakdown of the key highlights:
🔬 Iron Deficiency Anemia (IDA)
  • Cause: Inadequate iron → ↓ hemoglobin synthesis.
  • Labs: ↓ serum iron, ↓ ferritin, ↑ TIBC
  • Morphology: Microcytic, hypochromic RBCs
  • Notes: TIBC rises due to increased transferrin production in response to iron deficiency.
💥 Hemolytic Anemia
  • Cause: Premature RBC destruction—immune or non-immune mediated.
  • Labs: ↑ reticulocytes, ↑ LDH, ↑ indirect bilirubin, ↓ haptoglobin, (+) DAT (if immune-mediated)
  • Notes: Often associated with transfusion reactions, autoimmune hemolytic anemia, or certain infections/medications.
🧬 Sickle Cell Anemia
  • Cause: Mutation in the β-globin gene → Hgb S formation
  • Morphology: Sickle-shaped cells, target cells, anisopoikilocytosis
  • Labs: ↑ retic count, ↑ WBC/platelets, ↑ LDH/bilirubin, ↓ Haptoglobin
  • Genetics: Valine replaces glutamic acid at the 6th position of the β-globin chain.
🧪 Thalassemia
  • Cause: Decreased or absent synthesis of alpha or beta globin chains
  • Morphology: Microcytic, hypochromic RBCs; target cells; marked anisopoikilocytosis
  • Alpha Major: 4-gene deletion → hydrops fetalis
  • Beta Major: ↑ Hgb F and A2, ↓/absent Hgb A
  • Beta Minor: ↑ Hgb A2
  • Diagnosis: Hemoglobin electrophoresis
🚫 Aplastic Anemia
  • Cause: Bone marrow failure (acquired or inherited e.g. Fanconi anemia)
  • Labs: Pancytopenia, ↓ retic count
  • Bone Marrow: Hypocellular marrow
🔴 Hereditary Spherocytosis
  • Cause: Defects in RBC membrane proteins
  • Morphology: Spherocytes
  • Labs: ↑ MCHC, (+) Osmotic Fragility Test
🧪 G6PD Deficiency
  • Cause: X-linked recessive enzyme deficiency → RBCs vulnerable to oxidative stress
  • Triggers: Fava beans, certain drugs/infections
  • Morphology: Bite cells, blister cells, Heinz bodies, polychromasia
🥦 Megaloblastic Anemia
  • Cause: Vitamin B12 or folate deficiency → impaired DNA synthesis
  • Morphology: Macrocytic cells, hypersegmented neutrophils
  • Labs: ↓ B12/folate
💍 Sideroblastic Anemia
  • Cause: Impaired incorporation of iron into hemoglobin
  • Morphology: Ringed sideroblasts in bone marrow
  • Can be: Hereditary or acquired
  • MCV: May be microcytic or macrocytic
🧬 Anemia of Chronic Disease (ACD)
  • Cause: Chronic inflammation/infection → iron sequestration
  • Labs: ↓ serum iron, ↓ TIBC, normal or ↑ ferritin
  • MCV: Normocytic or microcytic
  • Mechanism: Cytokines disrupt iron metabolism; iron trapped in macrophages.
This guide is an efficient review tool: concise, high-yield, and ASCP-focused. Perfect to pair with your hematology study sessions or before practice questions.
If you’re having a hard time figuring out where to start studying, let’s book an onboarding call to get you a gameplan 🤗📚🧫https://calendly.com/microscopeviewsyt/free-onboarding-call
xoxo,
Marilyn
5
2 comments
Marilyn Virgo
5
🩸🥶 Anemias For The ASCP
Microscope Views (FREE)
skool.com/microscopeviewsfree
🧪🔬Helping Students Effectively Study For & Pass The ASCP Exam
Leaderboard (30-day)
Powered by