
Galactosemia: Bone Marrow Cell Vacuolization
Clinical case of galactosemia in an 8-month-old infant: GALT enzyme deficiency, bone marrow cell vacuolization, intoxication symptoms, and early cataracts.
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Clinical case of galactosemia in an 8-month-old infant: GALT enzyme deficiency, bone marrow cell vacuolization, intoxication symptoms, and early cataracts.

A suspected myeloproliferative neoplasm case: pancytosis in blood count, hyperplasia of hematopoietic lineages, and megakaryocyte nuclear fragments in bone marrow.

Morphological signs of dyserythropoiesis in bone marrow aspirate in MDS: cytoplasmic bridges, blasts, and binucleated cells amidst pancytopenia.

A rare clinical case of crystals found in megakaryocytes in a bone marrow aspirate of a 2-year-old child with infection and thrombocytopenia.

A clinical case of acute lymphoblastic leukemia in a 21-year-old patient: blast morphology in blood and bone marrow, MPO, PAS, and lipid cytochemistry results.

Clinical case of acute myelomonoblastic leukemia in a 61-year-old male: anemia, monocytosis in blood, and monocytoid blastosis in bone marrow aspirate.

A clinical case of erythroid leukemia in a cat. Morphological features of peripheral blood cells, increased white blood cell count.

Clinical case of suspected MDS: dyserythropoiesis, 10% blasts in bone marrow, cytopenia, and normoblasts in peripheral blood.

Blood smear morphology in suspected CML: leukocytosis 397×10⁹/L, left shift to blasts, basophilia, eosinophilia, Harlequin cells, and micromegakaryocytes.

Morphology of blasts in a peripheral blood smear from a patient with acute myeloid leukemia (AML) undergoing therapy: leukopenia and 21% blast cells.

A clinical case of multiple myeloma: rouleaux formation in peripheral blood smear and trinucleated plasma cells in bone marrow aspirate.

Bone marrow aspirate cytology in myelodysplastic syndrome: signs of dyserythropoiesis, binucleated erythroblasts, and megaloblastoid nuclei.