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Biomedical subjects

V M Popov

Publications and source records attributed to V M Popov.

At least 19 recordsLinked to original sources

[Pathomorphosis of acute leukemia].

Macro- and microscopic examinations of the viscera and hemopoietic organs of 405 dead patients who had suffered from various forms of acute leukemia were performed as well as microscopic investigations of 560 punch biopsies obtained from 372 patients at different stages of the disease. Pathomorphological findings on acute leukemias are presented, changes in the disease in the course of cytostatic antileukemia treatment are observed. Morphological signs of therapeutic pathomorphosis of acute leukemia involve: reduction or eradication of leukemic growths in the viscera and hemopoietic organs; hemopoietic hypo- and aplasia; dystrophic and necrobiotic alterations in the organs; topographic changes of leukemic proliferates (extramedullary localization of the process); augmentation of infectious and inflammatory complications; other causes of death.

Adult

[Characteristics of hematopoiesis in patients with the leukopenic syndrome].

The authors present data concerned with a long-term (up to 20 years) prophylactic medical observation over 103 patients with pronounced stable leukopenia. The different pathological processes associated with the development of the leukopenic syndrome were identified as were the reactive shifts in the medullary hemopoiesis of varying intensity. The shifts turned out nonspecific for all the disease entities under study.

Bone Marrow

[Preleukemia].

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Diagnosis, Differential

[Histopathology of lymphogranulomatosis].

The current histological classification of lymphogranulomatosis is presented. The possibility of the occurrence of the cellular phase of nodular sclerosis is discussed. In contrast to the current opinion on the origin of Berezovsky-Sternberg giant cells from reticular cells, the evidence in favour of their lymphocytic genesis is presented. Some problems of therapeutic pathomorphosis and thanatogenesis of patients with lymphogranulomatosis when current methods of treatment (radiation and polychemotherapy) are used are considered.

Histiocytes