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Aplastic Anemia — History and Physical — Clinical Pathway

Aplastic Anemia Clinical Pathway — All Settings

History and Physical

There are no specific physical findings in AA. Most children present with signs and symptoms resulting from advanced pancytopenia.

Physical examination: Findings consistent with acquired aplastic anemia

System Findings
General
  • Fatigue, exercise intolerance (anemia)
  • Fever (neutropenia)
Skin
  • Easy bruising, petechiae (thrombocytopenia)
  • Pallor (anemia)
Lymph
  • No LAD (pertinent negative)
HEENT
  • Epistaxis (thrombocytopenia)
GI
  • No hepatomegaly or splenomegaly (pertinent negative)
GU
  • Menorrhagia (thrombocytopenia)

History and physical: Findings that suggest an alternative diagnosis (such as inherited bone marrow failure syndrome)

Clinical History
  • Failure to thrive
  • Malabsorption/maldigestion
  • Developmental Delay
Family History
  • Family members with pancytopenia, especially if at early age
  • Squamous cell carcinomas, esp head and neck
  • Pulmonary fibrosis
  • Family members with physical exam findings suspicious for inherited bone marrow failure syndrome
Physical Examination
  • Short stature
  • Skin hyper- and hypopigmentation
  • Nail abnormalities
  • Limb (especially forearm) abnormalities
  • Other skeletal abnormalities
  • Renal and GU abnormalities
  • Cardiac abnormalities
  • Eye abnormalities
  • Cleft lip/palate
  • Hair or teeth abnormalities
  • Developmental delay

 

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