What is Leukopenia and Agranulocytosis? The proportion of leukopenic conditions among other diseases of the blood system is quite large. Statistics show an increase in the number of patients with severe leukopenia in recent years.
Continue readingWhat are the Patterns of Tumor Progression? Hemoblastosis has two stages: monoclonal (benign) and polyclonal – the occurrence of subclones (malignant). However, the change of stages is carried out with an unequal frequency in different
Continue readingWhat is Factor I Deficiency? Congenital and hereditary forms of fibrinogen deficiency are described as early as 1920. Family afibrinogenemia (absence of fibrinogen in the blood plasma) is a rare disease that is inherited in
Continue readingSymptoms of Autoimmune Hemolytic Anemia with Thermal Hemolysins This form of autoimmune hemolytic anemia, as a rule, begins gradually, in more rare cases, an acute onset is possible, the same as in the agglutinin form.
Continue readingWhat is Hemorrhagic Disease of the Newborn? During the first 4-7 days after birth, there is a decrease in the concentration of coagulation factors in the plasma. Early colostrum feeding can significantly alleviate this depression
Continue readingWhat is the Shenlein-Genoch disease? Hemorrhagic vasculitis is one of the most common hemorrhagic diseases, based on multiple microthrombuscovulitis, which affects the vessels of the skin and internal organs. The disease is often found in
Continue readingWhat is Hemolytic Anemia associated with a deficiency of glucose-6-phosphate dehydrogenase (G-6-FDG)? Hemolytic anemia associated with a deficiency of glucose-6-phosphate dehydrogenase (G-6-FDG) is a hereditary hemolytic anemia associated with a deficiency of enzyme activity. In
Continue readingWhat is Hairy Cell Leukemia? Hairy-cell leukemia is a rare variant of chronic leukemia, which is considered an independent nosological unit and is currently not considered as one of the clinical and morphological variants of
Continue readingWhat is the Rando-Osler Disease? Rando-Osler disease is the most common hereditary hemorrhagic vasopathy with focal thinning of the walls and expansion of the microvascular lumen, with inadequate local hemostasis. This pathology is inherited by
Continue readingWhat is Markiafavi-Micheli Disease? Markiafavi-Micheli’s disease is a rather rare form of acquired hemolytic anemia, characterized by a violation of the structure of erythrocytes, neutrophils and platelets, accompanied by signs of intravascular erythrocyte destruction. An
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