
Bone Marrow Erythroid Hyperplasia in Splenomegaly Case
A 56-year-old male with splenomegaly: complete blood count, erythroid expansion, and erythrocyte morphology in myelogram.
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A 56-year-old male with splenomegaly: complete blood count, erythroid expansion, and erythrocyte morphology in myelogram.

Morphological picture of bone marrow aspirate in acute leukemia relapse: blast cells 9.6% and marked erythroid hyperplasia up to 58.2%.

A rare morphological finding in bone marrow aspirate: a four-nucleated erythrocyte as a manifestation of dyserythropoiesis. Microscopic image.

Morphological criteria of proerythroblasts: nucleus structure, delicate reticular chromatin, nucleoli, and basophilic cytoplasm of erythroid cells.

Blood smear analysis in beta-thalassemia: massive normoblastosis (256 normoblasts), target cells, dacrocytes, and schistocytes in the differential count.

Bone marrow findings in severe anemia: erythroid hyperplasia, signs of dyserythropoiesis, and normoblast morphology in aspirate.

Peripheral blood smear in vitamin B12 deficiency: severe macrocytosis with MCV 130 fL, megalocytes, poikilocytosis, and nucleated red blood cells.

A morphological finding: a binucleated normoblast in a peripheral blood smear. Features of erythroid precursor cells during microscopy.

Peripheral blood smear in suspected B12 deficiency anemia: normoblasts with dyserythropoiesis, Howell-Jolly bodies, and basophilic stippling of erythrocytes.

Peripheral blood picture in beta-thalassemia after splenectomy: severe anisopoikilocytosis, target cells, normoblasts, and Howell-Jolly bodies.

Explore the morphology of a trinucleated normoblast in a bone marrow smear, indicating dyserythropoiesis. Understand the significance of erythroid lineage anomalies in laboratory diagnostics.

A 48-year-old myeloma patient's case: bone marrow erythroid hyperplasia, erythroblasts, macrophages, and megakaryocytes in aspirate smears.