
Pediatric B-Lymphoblastic Leukemia: A Diagnostic Case Study
A clinical case of B-ALL in an an 8-year-old child: leukopenia and anemia without blastemia, bone marrow blastosis, and B-ALL confirmation by flow cytometry.
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A clinical case of B-ALL in an an 8-year-old child: leukopenia and anemia without blastemia, bone marrow blastosis, and B-ALL confirmation by flow cytometry.

Morphology of Gaucher-like cells in a bone marrow smear from a patient with chronic myeloid leukemia (CML). Differential diagnosis and cytology.

A clinical case of CML detected during a routine blood test: hyperleukocytosis 203×10⁹/L, thrombocytosis, granulocyte maturation stages, and BCR-ABL1 mutation.

A clinical case of systemic mastocytosis: splenomegaly, urticaria pigmentosa, blood tryptase level >200 µg/L, and atypical mast cells in the bone marrow.

A clinical case of Hodgkin lymphoma: cytology of a lymph node biopsy, Reed-Sternberg cells, neutrophilic leukocytosis, and microcytic anemia.

Morphological features of peripheral blood cells in AML with chromosome 16 inversion: eosinophil dysplasia, promonocytes, and neutrophil hypogranulation.

A clinical case of acute erythroid leukemia: pancytopenia, blast cells in the smear, erythroid dysplasia, and flow cytometry (CD71+, CD235a+).

A clinical case of congenital sideroblastic anemia with HSPA9 mutation: blood picture, dyserythropoiesis, and ring sideroblasts in bone marrow.

A clinical case of CLL with marked leukocytosis (562×10⁹/L): prolymphocyte morphology in a blood smear and immunophenotyping data.

A clinical case of CLL: hyperleukocytosis 117×10⁹/L, thrombocytopenia, absolute lymphocytosis, and Botkin-Gumprecht shadows in peripheral blood.

A clinical case of thrombotic thrombocytopenic purpura: schistocytes in a blood smear, hemolysis, thrombocytopenia, and ADAMTS-13 deficiency.

A clinical case of pertussis in a 2-year-old child: pronounced lymphocytosis, lymphocytes with cleaved nuclei, and smudge cells in the blood smear.