
Tapeworm Diagnosis in Stool: A Clinical Case
A clinical case of a rare tapeworm identified by microscopy of a native stool sample in a child with chronic diarrhea and anemia.
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 clinical case of a rare tapeworm identified by microscopy of a native stool sample in a child with chronic diarrhea and anemia.

Why determine band neutrophils in the leukocyte formula: diagnosis of sepsis and SIRS, the link between band shift and mortality risk.

A clinical case of vitamin D-deficient rickets in an adolescent misdiagnosed as arthritis: 25(OH)D, parathyroid hormone, and alkaline phosphatase in diagnosis.

We discuss critical blood glucose levels, the consequences of severe hypoglycemia, and post-analytical errors in biochemical analysis reports.

A clinical case of bacteremia: detection of rod-shaped bacteria phagocytosed by neutrophils during digital microscopy of a peripheral blood smear.

The history of polychromatic blood smear staining: contributions of D. L. Romanowsky and Ch. I. Khentsinsky, mechanism, and ICSH recognition.

Peripheral blood smear findings in primary myelofibrosis: leucoerythroblastosis, dacryocytes, micromegakaryocytes, and giant platelets on microscopy.

Features of DNA double helix structure, principles of genetic material organization, and molecular diagnostic methods in the clinical laboratory.

A clinical case review: differentiating microcytic iron deficiency anemia and vitamin B12 deficiency based on MCV and ferritin levels.

How to describe chromatin structure in the cell nucleus: English classification of patterns and terminology options in Russian laboratory practice.

Genetic rearrangements of the KMT2A gene in acute myeloid leukemia: spectrum of partner genes according to the WHO 5th edition classification (WHO 2022).

An algorithm for the differential diagnosis of secondary arterial hypertension in children, including laboratory and instrumental search criteria.