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==Overview==
==Overview==

Revision as of 16:28, 7 September 2018

Sideroblastic anemia Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Nazia Fuad M.D.


Overview

Differential Diagnosis

Sideroblastic anemia must be differentiated from other causes of microcytic hypochromic anemia: iron deficiency anemia, thalassemia, anemia of chronic disease, lead poisoning, and blood loss.

• Tissue iron overload from sideroblastic anemia may act similar to hereditary hemochromatosis with liver cirrhosis, diabetes, congestive heart failure, and cardiac arrhythmias.

  • ALA Dehydratase Deficiency Porphyria
  • Acute Myeloid Leukemia (AML)
  • Congenital Erythropoietic Porphyria
  • Hereditary Coproporphyria
  • Iron Deficiency Anemia
  • Myelodysplastic Syndrome
  • Secondary Thrombocytosis


Diseases Clinical manifestations Para-clinical findings Gold standard
Symptoms Physical examination
Lab Findings
Pallor Weakness Jaundice Hepatomegaly Splenomegaly Growth retardation Peripheral blood smear Serum iron Serum TIBC Serum ferritin

g/L

Iron in erythroblasts Iron stores in bone marrow
Sideroblastic anemia + + variable Normal -high Normal 50-300 present in ring form present
Microcytic hypochromic

anemia

Iron deficiency anemia + + microcytic/

hypochromic

<30 > 360 <15 absent absent
Thalasemia jaundice + Hpatomegaly Splenomegaly Growth retardation micro/hypo with targeting Normal -high Normal 50-300 present present
Anemia of chronic disease Normal Low <300 30-200 absent present
Lead poisoning
Blood loss
Tissue iron overload

References

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