Table of contents |
Practical hematology of children's age
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Embryonal hemopoiesis
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Morfofunktsionalny characteristic of cells of marrow and peripheral blood
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Marrow parenchyma cells
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Etiology and pathogeny of leukoses
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Acute leukoses
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Acute leukoses - a preleukosis
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General principles of treatment of an acute leukosis
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Chemotherapeutic drugs
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Treatment of an acute lymphoblastoid leukosis
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Treatment of myeloid forms of an acute leukosis
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Infectious complications and symptomatic therapy of an acute leukosis
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Consolidation and maintenance therapy of an acute leukosis
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Immunotherapy
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Remission and recurrence of an acute leukosis
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Inborn leukosis
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Neuroleukosis
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Myelosis
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Lymphogranulomatosis
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Gematosarkoma
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Macrofollicular lymphoma
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Angioimmunoblastny lymphadenopathy
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Leukemoid tests
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Infectious lymphocytosis
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Infectious mononucleosis
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Leukemoid tests of different types
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Dysfunctions of granulocytes
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Leukopenias
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Histiocytoses
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Histiocytoses - an eosinophilic granuloma
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Malignant histiocytosis
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Family erythrophagocytal histiocytosis
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Accumulation diseases
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Nimann's illness — Peak
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Angiopathies
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Hemorrhagic vasculitis (Shenleyn's illness — Genokh)
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Mayokki's purpura
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Ataxy teleangiectasia
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Entsefalotrigeminalny angiomatosis
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Kortiko-meningealny diffusion angiomatosis
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Cerebroretinal angiomatosis
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Hypertrophic gemangiektaziya
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Multiple and huge hemangiomas
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Elastic fibrodisplaziya
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Coagulopathies
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Hereditary coagulopathies
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Hemophilia And
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Clinic of hemophilia
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Treatment of hemophilia
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Angiohemophilia
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Cristmas disease (Kristmas's illness)
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Hereditary deficit of factors of XI, XII, XIII and I
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Dysfibrinogenemias
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Hereditary deficit of factors of VII, X, V and II
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Deficit K-vitaminozavisimykh of factors of coagulation
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Syndrome of the disseminated intravascular coagulation
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Clinic and diagnosis of the IDCS
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Treatment of the IDCS
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Thrombocytopenia
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Idiopathic Werlhof's disease
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Clinic and diagnosis of an idiopathic Werlhof's disease
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Treatment of an idiopathic Werlhof's disease
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Isoimmune Werlhof's disease
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Transimmune Werlhof's disease of newborns
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Trombogemolitichesky Werlhof's disease (syndrome Moshkovich)
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Hereditary Werlhof's diseases
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Trobotsitopatiya
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Anemias
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The anemias connected with blood loss
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Chronic posthemorrhagic anemia
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Iron deficiency anemias
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Clinic and diagnosis of an iron deficiency anemia
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Treatment of iron deficiency anemias
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Sideroakhrestichesky, sideroblastny anemias
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Megaloblastny anemias
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Foliyevodefitsitny anemia
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Hereditary forms of megaloblastny anemias
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Hereditary dizeritropoetichesky anemias
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The anemias connected with oppression of proliferation of cells of marrow
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Hereditary hypoplastic anemias
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Hemolitic anemias
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Hemolitic anemias - an ovalocytosis, a hereditary stomatocytosis
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Acanthocytosis, piknotsitoz
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The hereditary hemolitic anemias connected with disturbance of activity of enzymes of erythrocytes
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The hereditary hemolitic anemias connected with disturbance of structure or synthesis of hemoglobin
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The acquired immune hemolitic anemias
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Isoimmune hemolitic anemias
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Treatment of a hemolitic illness of newborns
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Autoimmune hemolitic anemias
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List of references
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Page 8 of 93
Acute leukosis — a malignant tumor which pathological substrate is provided by young people, or blast, cells. At children's age the acute leukosis in most cases meets. Many decades establishment of the diagnosis of an acute leukosis meant the unfavourable forecast. Rough increase of clinical signs, development of anemia, a hemorrhagic syndrome, necrotic changes, infectious complications within several months led to a lethal outcome. Modern development of science, development of means of polychemotherapy allow to approach treatment of this pathology more optimistically. Also the fact that the best results of treatment of an acute leukosis are achieved at children is pleasant. At an acute lymphoblastoid leukosis the percent of remissions at patients comes nearer to 100. According to the domestic and foreign children's hematologic centers, at a half of children 5 years' remissions are received. About 5% of children have superlong (7 — 10 years) remissions that allows to carry this contingent to recovering from an acute leukosis. Search of objective criteria of classification of acute leukoses is conducted constantly. Experience demonstrates that morphological features cannot serve as objective criterion of differentiation. At modern therapy of leukoses, considerable extension of life of patients morphological forms of leukemic cells change. The stablest sign are cytochemical properties of blast cells which reflect features of an exchange and are individual at each look. Cytochemical criteria also are the basis for classification of acute leukoses. Different authors offer several options of classifications, however they have no basic character. Allocation of such forms of acute leukoses as lymphoblastoid, miyeloblastny, monoblast, miyelomonoblastny, promiyelotsitarny, an erythremic myelosis and a nondifferentiable form does not raise doubts. The cytochemical characteristic of these forms is provided to tab. 6.
Table 6. Cytochemical characteristic of various options of an acute leukosis (E. N. Mosyagina, N. A. Torubarov, E. B. Vladimirskaya, 1981).
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|
Cytochemical characteristic |
|
|
Option: acute leukosis |
Per- oksi- basin |
Reaction to lipids with Sudan black |
Turned sour bark fos- veil - for |
chic - reaction to a glycogen |
a-Naftil- esterase |
Hloratse- tatestera- for |
Acid sulfati- rovanny mukopoli- saccharites |
Lymphoblastoid |
_ |
_ |
± |
+ |
|
|
|
Miyeloblastny |
+ |
+ |
+ |
+ |
|
+ |
— |
Monoblast
|
± |
± |
++ |
± |
+ |
— |
— |
Miyelomonoblastny
|
+ |
± |
+ |
± |
+ |
± |
— |
Promiyelotsitarny
|
++ |
+ |
± |
+ + |
± |
++ |
+ |
Nondifferentiable |
— |
— |
— |
— |
— |
— |
— |
Note: N-----reaction positive, ± — slabopolozhitelny,----------------negative.
For practical purposes it should be noted importance of allocation and differentiation of a lymphoblastoid form and group of the miyelomonoblastny nature. Tactics of treatment of the acute lymphoblastoid leukosis which is the most frequent form at children is other than that at other forms of an acute leukosis whereas acute miyeloblastny, monoblast and miyelomonoblastny leukoses are treated according to similar programs. Also the acute promiyelotsitarny leukosis having features of therapeutic tactics is subject to allocation. In classification of acute leukoses such forms as an erythroleukosis, an eosinophilic leukosis, a basphilic leukosis, plazmoblastny option, megakarioblastny option, a low-percentage form of an acute leukosis meet. However allocation of some forms remains diskutabelny, other forms in pediatric practice do not meet. The clinical course of an acute leukosis at children under the influence of modern methods of therapy underwent qualitative changes. From quickly progressing acute process the leukosis passed into the category of diseases with a long wavy current. Allocate the next periods of a disease: initial, period of a full course of a disease, remission, aggravation and terminal. Now the period of remission is considered obligatory, especially at children with an acute lymphoblastoid leukosis. Long remission (more than 5 years) allows to speak about recovery. Return to kliniko-hematologic displays of an illness is treated as to pass the recurrence of an acute leukosis able into an end-stage. At an acute lymphoblastoid leukosis at children recurrence of a disease can be stopped and transferred to a remission phase, however, already in smaller percent of cases again, than during the first attack. Allocation of the periods of leukemic process has practical value as in many respects defines the forecast of a disease and therapeutic tactics.
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