
Stool Microscopy Challenge: Identifying Findings
A diagnostic challenge in stool microscopy for an adult patient: help identify the origin of the structures found in a native preparation.
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.

A diagnostic challenge in stool microscopy for an adult patient: help identify the origin of the structures found in a native preparation.

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

Clinical case of myeloproliferation in a 48-year-old female patient. Description of bone marrow findings from sternal puncture and peripheral blood data.

Comparative characteristics of major immunoglobulin classes (IgG, IgA, IgM, IgD, IgE): molecular structure, subclasses, concentration, and half-life.

Reference ranges and cut-off levels for BNP and NT-proBNP in heart failure exclusion and confirmation, and indications for echocardiography.

Morphology of prolymphocytes in peripheral blood with Romanowsky staining: differential diagnosis with lymphocytes and blasts in blood smears.

Critical levels of total and direct bilirubin in adult patients' biochemical blood tests: visual assessment of pronounced icteric serum.

Erythrocyte morphology in sickle cell anemia: detection of drepanocytes, polychromatophilia, and normoblasts in a peripheral blood smear.

Morphology and causes of macrothrombocytes and giant platelets in blood smears: differential diagnosis in pancytosis and thrombocytopathies.

A clinical microscopy challenge: unusual large objects found in a gynecological smear from a 33-year-old woman. Methylene blue stain.

Clinical case of MYH9-associated thrombocytopenia: macrothrombocytes, neutrophil inclusions, differential diagnosis with ITP, and genetic confirmation.

A clinical case of idiopathic hypereosinophilic syndrome: diagnostic criteria, bone marrow examination, and mepolizumab therapy.