Excellent. I now have comprehensive CBC content. Here is a full breakdown:
Complete Blood Count (CBC)
A CBC is one of the most commonly ordered laboratory panels. It quantifies and characterizes the cellular and formed elements of blood - erythrocytes, leukocytes, and thrombocytes - typically analyzed by automated flow cytometry-based cell counters that examine ~10,000 cells per category for high accuracy.
Components of the CBC
1. White Blood Cell (WBC) / Leukocyte Count
| Finding | Term | Common Causes |
|---|
| Elevated WBC | Leukocytosis | Infection, inflammation, burns, fractures, stress, pregnancy, labor |
| WBC >100 x 10⁹/L | Hyperleukocytosis | Leukemia |
| Decreased WBC | Leukopenia | Chemotherapy, radiation, autoimmune disease, aplastic anemia, antipsychotics, antiepileptics, immunosuppressants, HIV/AIDS |
2. WBC Differential
The differential reports the percentage of each leukocyte type:
- Neutrophils (including band cells - immature neutrophils)
- Eosinophils
- Basophils
- Lymphocytes
- Monocytes
Absolute counts are important - for example, absolute lymphocyte count primarily reflects T-cell status since ~90% of circulating lymphocytes are T cells. The minimum expected count is >1,500 small lymphocytes/mm³.
Specific differentials to know:
- Low ANC (absolute neutrophil count): suggests neutropenia/immunodeficiency
- Elevated eosinophils: seen in Omenn syndrome, hyper-IgE syndrome
- Low monocytes: associated with GATA2 deficiency
- Large vacuoles in neutrophils: Chediak-Higashi syndrome
3. Red Blood Cell (RBC) / Erythrocyte Count
| Finding | Term | Common Causes |
|---|
| Elevated RBC | Polycythemia | Polycythemia vera (primary), chronic hypoxia, high altitude, EPO-secreting tumor (secondary) |
| Decreased RBC | Anemia | Bleeding, iron/B12 deficiency, poor nutrition, pregnancy, chronic disease, sickle cell anemia |
4. Hemoglobin (Hgb)
Reflects the oxygen-carrying capacity of blood.
| Population | Normal Range |
|---|
| Males | 13.5 - 17.5 g/dL (140 - 180 g/L) |
| Females | 12 - 15.5 g/dL (120 - 150 g/L) |
Hgb and hematocrit (HCT) are the two key tests for evaluating anemia vs. polycythemia.
5. Hematocrit (HCT) / Packed Cell Volume (PCV)
The percentage of total blood volume occupied by red blood cells.
6. RBC Indices (automatically calculated)
| Index | What it Measures | Clinical Use |
|---|
| MCV (Mean Corpuscular Volume) | Size of RBCs | Micro vs. normocytic vs. macrocytic anemia |
| MCH (Mean Corpuscular Hemoglobin) | Amount of Hgb per average RBC | Hypochromic vs. normochromic |
| MCHC (Mean Corpuscular Hgb Concentration) | % Hgb concentration in average RBC | Severity of hypochromia |
| RDW (Red Cell Distribution Width) | Variation in RBC size/shape (anisocytosis) | Differentiating types of anemia |
7. Platelet (Thrombocyte) Count
| Finding | Term | Common Causes |
|---|
| Elevated platelets | Thrombocythemia | Bone marrow proliferative disorders, inflammation, post-splenectomy, hyposplenism |
| Decreased platelets | Thrombocytopenia | Leukemia, B12 deficiency, infections, hereditary syndromes, autoimmune disease, DIC, certain medications |
MPV (Mean Platelet Volume): measures average platelet size; large platelets suggest increased platelet turnover (e.g., ITP).
Special finding: small platelets are seen in Wiskott-Aldrich syndrome.
How the CBC is Performed
Blood is diluted in suspension fluid and passed as a thin stream through narrow tubing. A light detector and electrical impedance sensor identify cell types by size and resistance. Modern analyzers use computer-assisted image processing. Manual microscopy is still used in select cases (e.g., to identify blast cells, atypical lymphocytes, or Howell-Jolly bodies).
Clinically Important Peripheral Smear Findings (complement to CBC)
| Finding | Associated Condition |
|---|
| Large vacuoles in neutrophils | Chediak-Higashi syndrome |
| Small platelets | Wiskott-Aldrich syndrome |
| Howell-Jolly bodies | Functional asplenia |
| Thrombocytopenia + anemia | Autoimmune lymphoproliferative syndrome, CVID, 22q11.2 deletion |
| Autoimmune hemolytic anemia | Wiskott-Aldrich syndrome |
Sources: Histology: A Text and Atlas with Correlated Cell and Molecular Biology, pp. 728-730 | Henry's Clinical Diagnosis and Management by Laboratory Methods, p. 1175