II. History
- See Iron Deficiency Anemia for related history
- 
                          Family History of Anemia- Hereditary Spherocytosis
- Sickle Cell Anemia (Black patients)
- Thalassemia (Asian, Black, or Mediterranean patients)
- Other Hemoglobinopathy
- Glucose-6-Phosphate Dehydrogenase Deficiency (G6PD)- Black, Greek, Filipino, Jewish, Sardinian patients
- X-linked inheritance (consider in males)
 
 
- History of chronic illness (Anemia of Chronic Disease)- Chronic infection
- Collagen vascular disease
- Malignancy
- Hypothyroidism
- Hypoadrenalism
- Renal disease
- Hypopituitarism
 
- Dietary habits- Inadequate Iron or Protein intake: Iron Deficiency
- Strict Vegetarian: Vitamin B12 Deficiency
- Diet lacking fruits and vegetables: Folate Deficiency
 
- History of Gastrectomy or Malabsorption (e.g. Diarrhea)
- Recent Infection- Parvovirus: Erythroblastopenia
- Hepatitis: Aplastic Anemia
 
- Medications- See Medication Causes of Macrocytic Anemia
- Oxidant medications provoke G6PD
 
- 
                          Abdominal Pain
                          - Peptic Ulcer Disease
- Lead Toxicity
- Porphyria
 
- 
                          Pica
                          - Suggests Iron Deficiency Anemia
 
III. Symptoms
- Many patients are asymptomatic- Mild Anemia (Hemoglobin over 10 g/dl)
- Gradual onset of Anemia
- Active, well-conditioned persons
 
- Non-specific Symptoms- Fatigue
- Generalized weakness
- Dyspnea on exertion
- Light headed
- Pruritus (Iron Deficiency Anemia)
 
IV. Signs: Anemia
- 
                          Vital Signs- Tachycardia
- Systolic Murmur (ejection murmur)
 
- Thorough, systematic exam for Anemia cause- Abdominal and pelvic exam
- Rectal Exam with Stool Guaiac for occult blood
 
- Pallor in severe Anemia (Hct <25%, Hgb <7 g/dl)- Pale Conjunctiva or mucous membranes
- Pallor at the nail beds or palmar creases
 
V. Signs: Clinical Clues
- 
                          Jaundice
                          - Hemolytic Anemia
- Hepatitis
 
- Angular Cheilitis
- Glossitis
- 
                          Splenomegaly
                          - Chronic Hemolytic Anemia
- Acute infection
- Leukemia
- Lymphoma
- Portal Hypertension
 
- Frontal bossing with prominent malar and Maxillary Bone- Chronic Hemolytic Anemia
 
- Neurologic changes (Dementia, Ataxia, Paresthesias)
VI. References
- Oblender in Daeschner (1991) Pediatrics, p. 281
- Irwin (2001) Am Fam Physician 64(8):1379-86 [PubMed]
