Blood diseases constitute a numerous and heterogeneous group of syndromes that develop with violations of the qualitative and quantitative composition of blood. The practical direction developing the principles of diagnosis and treatment of blood diseases is hematology and its separate branch – oncohematology. Specialists who carry out correction of the state of blood and hematopoietic organs are called hematologists. Hematology has the closest interdisciplinary connections with internal diseases, immunology, oncology, and transfusiology.

Since ancient times, in many cultures, human blood was endowed with mystical properties, symbolized the divine source and flow of life. “Precious”, “hot”, “innocent”, “young”, “royal” – whatever properties people gave blood, and the epithet “blood” always meant the highest degree of certain manifestations – blood kinship, blood enemy, blood grudge, blood revenge.

Meanwhile, from the point of view of physiology, blood is a liquid medium of the body that continuously circulates through the vascular system and performs a number of important functions – respiratory, transport, regulatory, protective, etc. Blood consists of a liquid fraction – plasma and shaped elements suspended in it – blood cells (erythrocytes, platelets and leukocytes). The main organs of hematopoiesis (hemocytopoiesis), which are a kind of “factory” for the production of blood cells, include the red bone marrow, thymus, lymphoid tissue and spleen. Blood diseases are spoken of in the case of a violation of the morphology or the number of certain blood cells or changes in the properties of plasma.

All diseases of the blood and hematopoietic system are classified based on the defeat of one or another of its components. In hematology, blood diseases are usually divided into three large groups: anemia, hemoblastosis and hemostasiopathy. So, frequent anomalies and lesions of erythrocytes include deficient, hemolytic, hypo– and aplastic anemia. The structure of hemoblastoses includes leukemias and hematosarcomas.

Blood diseases associated with damage to the hemostatic system (hemostasiopathy) include hemophilia, Willebrand’s disease, thrombocytopathies, thrombocytopenia, DIC syndrome, etc.

Blood diseases can be congenital and acquired in nature. Congenital diseases (sickle cell anemia, thalassemia, hemophilia, etc.) are associated with gene mutations or chromosomal abnormalities. The development of acquired blood diseases can be triggered by numerous environmental factors: acute and chronic blood loss, exposure to ionizing radiation or chemical agents, viral infections (rubella, measles, mumps, influenza, infectious mononucleosis, typhoid fever, viral hepatitis), nutritional deficiency, impaired absorption of nutrients and vitamins in the intestine, etc. When bacterial or fungal agents enter the bloodstream, a serious blood disease of infectious genesis occurs – sepsis. Many blood diseases go hand in hand with collagenoses.

The manifestations of blood diseases are many-sided and not always specific. Characteristic signs of anemia are causeless fatigue and weakness, dizziness up to fainting, shortness of breath during physical exertion, pallor of the skin. Disorders of the blood coagulation link are characterized by petechial hemorrhages and ecchymoses, various kinds of bleeding (gingival, nasal, uterine, gastrointestinal, pulmonary, etc.). In the leukemia clinic, intoxication or hemorrhagic syndromes come to the fore.

The very first method with which the diagnosis of blood diseases begins is the study of a hemogram (clinical analysis) with the determination of the quantitative composition of blood and the morphology of the shaped elements. In blood diseases occurring with hemostasis disorders, the number of platelets, blood clotting and bleeding time, prothrombin index, coagulogram are examined; various kinds of tests are carried out – a tourniquet test, a pinch, a cupping test, etc.

To assess the changes occurring in the hematopoietic organs, bone marrow puncture (sternal puncture, iliac puncture, trepanobiopsy) is used with the study of its cellular composition. In connection with blood diseases, other invasive diagnostic interventions may be performed: biopsies of the lymph nodes and spleen to clarify the relationship between the central and peripheral hematopoietic organs.

Radiation research methods (chest X-ray and CT, radiography of tubular bones) are used to detect enlarged mediastinal lymph nodes in lymphogranulomatosis, lymphosarcoma, lymphocytic leukemia; bone lesions in lymphomas, myeloma, etc. To assess the size, function of the spleen and identify its focal lesions, scintigraphy is performed. As part of the investigation of the causes of the anemia syndrome, patients may need to consult a gastroenterologist and gynecologist; FGDS, colonoscopy, liver ultrasound.

Any changes in the hemogram or myelogram, as well as symptoms indicating the likelihood of developing blood diseases, require a competent assessment by a hematologist, dynamic observation or specialized treatment under his supervision. Modern hematology has developed the fundamental principles of therapy for various blood diseases and has accumulated vast experience in their cure. If possible, the treatment of blood diseases begins with the elimination of causes and risk factors, correction of internal organs, replenishment of missing substances and trace elements (iron – with iron deficiency anemia, vitamin B12 – with B12 deficiency anemia, folic acid – with folic deficiency anemia, etc.).

In some cases, corticosteroids, hemostatic drugs, extracorporeal hemocorrection (plasmapheresis, erythrocytapheresis) may be indicated. Often, hematological patients need blood transfusion and its components.

Cytostatic therapy, radiotherapy, allogeneic and autologous bone marrow transplantation, and the introduction of stem cells are the most relevant and effective methods of treating hematoblastosis worldwide. A number of blood diseases (thrombocytopenic purpura, autoimmune anemia, myeloid leukemia, etc.) are indications for spleen removal – splenectomy.

With the current level of development of medical science, most blood diseases can be cured and prevented. To do this, it is necessary to take a general blood test every year, immediately consult a doctor when the first alarming symptoms appear, do not start the course of chronic diseases (erosive gastritis, gastric ulcer, enteritis, NYAK, hemorrhoids, uterine fibroids, etc.). It is necessary to avoid exposure to adverse environmental factors on the body. To exclude the birth of offspring with congenital blood diseases, medical and genetic consultations are conducted.
In this section of the medical reference book “Medic Journal” you will be able to find answers to the main questions concerning blood diseases, get acquainted with the main nosological forms, symptoms, principles of diagnosis and treatment.

Sideroblastic Anemia

Sideroblastic anemia is an acquired or hereditary blood disease characterized by hypochromia of erythrocytes, high levels of serum iron with deposition in the tissues of organs. The clinical picture is represented by anemic syndrome (dizziness, fatigue, pallor of the skin), hemosiderosis of internal organs (hepatomegaly, cardiomegaly, CRF), a change in the blood picture. The diagnosis…

Sickle Cell Anemia

Sickle cell anemia is a hereditary hemoglobinopathy caused by the synthesis of abnormal hemoglobin S, a change in the shape and properties of red blood cells. Disease is manifested by hemolytic, aplastic, sequestration crises, vascular thrombosis, bone and joint pain and swelling of the extremities, skeletal changes, splenic and hepatomegaly. The diagnosis is confirmed by…

Sepsis

Sepsis is a common purulent infection that develops due to the penetration and circulation of various pathogens and their toxins in the blood. The clinical picture of sepsis consists of intoxication syndrome (fever, chills, pale earthy coloration of the skin), thrombohemorrhagic syndrome (hemorrhages into the skin, mucous membranes, conjunctiva), metastatic lesions of tissues and organs…

Senile Purpura

Senile purpura are small bruises that occur in the elderly due to increased fragility of blood vessels and other age—related changes in the structure of the skin. Predisposing factors include the influence of ultraviolet radiation, anticoagulant therapy. The disease is manifested by bruises, which are usually located on the hands and appear for no apparent…

Posthemorrhagic Anemia

Posthemorrhagic anemia is a complex of clinical and hematological changes resulting from acute or chronic blood loss. Disease is characterized by pallor, shortness of breath, darkening of the eyes, dizziness, hypothermia, arterial hypotension; in severe cases – lethargy, thready pulse, shock, loss of consciousness. Pathology is diagnosed according to the clinical picture and a blood…

Polycythemia

Polycythemia is a chronic hemoblastosis, which is based on the unlimited proliferation of all myelopoiesis sprouts, mainly erythrocyte. Clinically, polycythemia is manifested by cerebral symptoms (heaviness in the head, dizziness, tinnitus), thrombohemorrhagic syndrome (arterial and venous thrombosis, bleeding), microcirculatory disorders (limb chilliness, erythromelalgia, hyperemia of the skin and mucous membranes). Basic diagnostic information is obtained…

Plasmocytoma

Plasmocytoma is a malignant tumor of plasma cells that affects bones and internal organs. The disease can occur in a solitary form in the presence of only one pathological focus or in a generalized version, when different body systems are involved in the process. Plasmocytoma is characterized by a variety and non-specificity of clinical symptoms,…

Paroxysmal Nocturnal Hemoglobinuria

Paroxysmal nocturnal hemoglobinuria is a rare life–threatening hematological disease characterized by intravascular hemolysis, arterial and venous thrombosis, systemic damage to internal organs. The clinical picture is diverse. The most typical symptoms include general weakness, paroxysmal abdominal, lumbar pain, darkening of urine. The main diagnostic method is flow cytometry (reduced expression of GPI–bound proteins on blood…

Pernicious Anemia

Pernicious anemia is a violation of the red germ of hematopoiesis caused by a lack of cyanocobalamin (vitamin B12) in the body. With B12-deficient anemia, circulatory hypoxic (pallor, tachycardia, shortness of breath), gastroenterological (glossitis, stomatitis, hepatomegaly, gastroenterocolitis) and neurological syndromes (impaired sensitivity, polyneuritis, ataxia) develop. Confirmation is made based on the results of laboratory studies…

Pancytopenia

Pancytopenia is a decrease in the number of all shaped elements in the peripheral blood. The condition is one of the signs of bone marrow insufficiency that occurs with aplastic anemia, leukemia, the action of ionizing radiation. Pathology is manifested by anemia, immunodeficiency, hemorrhagic syndrome. To diagnose pancytopenia, a blood test, examination of bone marrow…