Imágenes para exposición de anemias

A, Normal red cells.

A, Normal red cells.

B, Microcytic hypochromic cells typical of iron deficiency

B, Microcytic hypochromic cells typical of iron deficiency

B, Microcytic hypochromic cells typical of iron deficiency

C, Macrocytosis typically seen in megaloblastic anemia.

C, Macrocytosis typically seen in megaloblastic anemia.

D, Target cells

D, Target cells

E, Schistocytes and nucleated red

cells.

E, Schistocytes

E, Nucleated Red Cells

• F, Rouleaux formation.

• F, Rouleaux formation.

G, Normal red cells and microspherocytes in

hereditary spherocytosis.

G, Normal red cells and microspherocytes in hereditary spherocytosis.

H, Sickle cell anemia, showing sickled cells, a

Howell-Jolly body, and polychromatophilia.

I, Teardrop poikilocytes.

I, Teardrop poikilocytes.

J, Reticulocytes (special stain).

J, Reticulocytes.

K, Howell-Jolly body (nuclear remnant).

K, Howell-Jolly bodies.

L, Homozygous β-thalassemia, showing microcytic and hypochromic erythrocytes, anisocytosis and poikilocytosis, basophilic stippling, a

Howell-Jolly body, target cells, and polychromatophilia.

M, Heterozygous β-thalassemia, showing

hypochromia and microcytosis.

M, Heterozygous β-thalassemia, showing

hypochromia and microcytosis.

N, Sickle cell disease

N, Pappenheimer bodies.

• O, Eccentrocytes (blister cells) with a lopsided distribution of hemoglobin. Typically seen during a hemolytic episode in glucose-6-phosphate dehydrogenase (G6PD) deficiency.

• O, Eccentrocytes (blister cells) with a lopsided distribution of hemoglobin. Typically seen during a hemolytic episode in glucose-6-phosphate dehydrogenase (G6PD) deficiency.