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Macrocytic anemia physical examination

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Shyam Patel [2]; Associate Editor(s)-in-Chief: Amandeep Singh M.D.[3] Omer Kamal, M.D.[4]

Overview

Overview

Common physical examination findings of megaloblastic anemia include glossitis, pallor, mouth ulcers, vitiligo, subacute combined degeneration, and positive Romberg’s sign.

Physical Examination

Physical Examination

Physical examination includes the following: [1][2][3]

Appearance of the Patient

  • Patients with megaloblastic anemia usually appear pale and fatigued

Vital Signs

  • High-grade / low-grade fever
  • Tachycardia with regular pulse
  • Weak/bounding pulse / pulsus alternans / paradoxical pulse / asymmetric pulse

Skin

HEENT

Neck

  • Neck examination of patients with megaloblastic anemia is usually normal but can sometimes show thyromegaly is hypothyroidism or hyperthyroidism are the causes of megaloblastic anemia.

Lungs

Heart

Abdomen

  • Abdominal examination of patients with megaloblastic anemia is usually normal but can sometimes show hepatomegaly if liver disease is the cause of megaloblastic anemia.

Back

  • Back examination of patients with megaloblastic anemia is usually normal.

Genitourinary

  • Genitourinary examination of patients with megaloblastic anemia is usually normal.

Neuromuscular

Extremities

References

References

  1. Nagao T, Hirokawa M (October 2017). “Diagnosis and treatment of macrocytic anemias in adults”. J Gen Fam Med. 18 (5): 200–204. doi:10.1002/jgf2.31. PMC 5689413. PMID 29264027.
  2. Shojania AM (May 1980). “Problems in the diagnosis and investigation of megaloblastic anemia”. Can Med Assoc J. 122 (9): 999–1004. PMC 1801696. PMID 6768440.
  3. Rauw J, Wells RA, Chesney A, Reis M, Zhang L, Buckstein R (October 2011). “Validation of a scoring system to establish the probability of myelodysplastic syndrome in patients with unexplained cytopenias or macrocytosis”. Leuk. Res. 35 (10): 1335–8. doi:10.1016/j.leukres.2011.05.001. PMID 21704372.
  4. Devalia V, Hamilton MS, Molloy AM (August 2014). “Guidelines for the diagnosis and treatment of cobalamin and folate disorders”. Br. J. Haematol. 166 (4): 496–513. doi:10.1111/bjh.12959. PMID 24942828.


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