
Auer Rods in Blasts in Acute Myeloid Leukemia
Clinical case of acute myeloid leukemia in a 15-year-old teenager: Auer rods in blasts, pancytopenia, leukocytosis, and analyzer scattergram.
Blood and bone marrow morphology, clinical cases and diagnostic algorithms. Most of the library is in Russian; the English section is growing.
Most of our material is written in Russian — that is the working language of the community. A few pieces exist in English; the rest of the library is one click away and the photographs need no translation.

Clinical case of acute myeloid leukemia in a 15-year-old teenager: Auer rods in blasts, pancytopenia, leukocytosis, and analyzer scattergram.

Clinical case of CML: 7% blasts, myelocytes, and metamyelocytes in CBC. Cell morphology and the importance of blast count in myeloid leukemia.

Morphological features of blasts in acute lymphoblastic leukemia L3 (FAB) and Burkitt lymphoma: cytoplasmic basophilia, pronounced cell vacuolization.

Clinical case: atypical mononuclear cells (32%) and leukocytosis 21.38×10⁹/L in a 23-year-old female patient. Sysmex WDF and WPC scattergrams, cytology, and leukocyte differential.

Morphological features of blasts in blood: high nuclear-cytoplasmic ratio, delicate chromatin, and the role of immunophenotyping in diagnosis.

Morphological features of atypical mononuclear cells (virocytes) in blood smears: nuclear polymorphism, cytoplasmic basophilia, and infection diagnosis.

Diagnostic criteria and morphological features of AML with t(8;21) translocation: blast assessment, granulocyte anomalies, and differential diagnosis with APL.

Criteria for differential diagnosis of AML with t(8;21), acute promyelocytic leukemia, and CMML: bone marrow cytology, immunophenotyping, and genetics.

A clinical case of hairy cell leukemia: morphology of neoplastic lymphocytes in peripheral blood smear, including scalloped and filiform cell forms.

A clinical case of hairy cell leukemia in a 65-year-old man: complete blood count parameters, scattergram, and morphology of scalloped and filamentous cells.

A case of CLL transformation to prolymphocytic leukemia: leukocytosis increased to 162×10⁹/L in 4 months, with up to 40% prolymphocytes in blood smear.

Rendu-Osler disease: causes of endothelial insufficiency, skin and mucous membrane telangiectasias, risk of occult GI bleeding and iron deficiency anemia.