
Cystine Crystals in Urine Sediment in Cystinuria
Characteristic hexagonal cystine crystals in acidic urine sediment: microscopic features, formation mechanism, and clinical significance in cystinuria.
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.

Characteristic hexagonal cystine crystals in acidic urine sediment: microscopic features, formation mechanism, and clinical significance in cystinuria.

Morphology of green crystals of death in neutrophils: the significance of blue-green inclusions, Döhle bodies, and bacteremia in severe sepsis.

Cytological findings of a fine-needle aspirate of the thyroid gland in Hashimoto's thyroiditis: Hürthle cell clusters with atypia and lymphoid infiltration.

Microscopic appearance of neutral fat in stool in steatorrhea: comparison of native preparation and methylene blue staining in coprogram.

Mechanisms of antiparasitic immune response: role of Th2 lymphocytes, IgE secretion, and activation of eosinophils with release of cytotoxic granule proteins.

Clinical case of primary myelofibrosis: dysplastic megakaryocyte, dacryocytes, and blasts found in peripheral blood, JAK2 V617F mutation.

Cultivation and micromorphology of Aspergillus niger: colony growth on Sabouraud agar and conidiophore structure under microscopy.

A case of cold agglutination: false MCHC elevation, sample appearance in tube and microscopy, and parameter correction after 37°C incubation.

The importance of the preanalytical stage in general urinalysis: rules for biomaterial collection, transportation conditions to the laboratory, and common errors.

Microscopic examination of stool with Lugol's solution: detection of mycelial filaments and clusters of yeast spores in a child with COVID-19.

A clinical case of primary myelofibrosis with JAK2 V617F mutation: analysis of analyzer hemogram, leucoerythroblastic picture, dacryocytes, and cell atypia.

Learn about Chédiak–Higashi Syndrome: LYST gene mutation, giant granules in neutrophils on blood smear microscopy, and partial albinism.