- •Pathophysiology tasks:
- •General doctrine of disease. Basic concepts of general pathology: norm, health. Definition by who. Disease.
- •Disease.
- •Conception of pathological process, pathological state, pathological reaction. Definition of typical pathological processes.
- •Typical pathological processes are the processes which are developed by similar laws, independently on reasons, localization, animals type and organism individual peculiarities.
- •Disease difference from health
- •3 Points of view:
- •Disease, biological and social factors are actual because human being is first of all social creature
- •4 Levels of diseases prescription:
- •5. Diseases classification principles:
- •8. Collapse. Comparative characteristics with shock. Aethiology and pathogenesis. Role of nervous and humoral mechanisms
- •9. Crash-syndrome -
- •10. Coma -
- •11. Informational aspects of cell injury. Pathology of signalization.
- •13. Programmed cell death (pcd)
- •3 Apoptosis phases:
- •14. Outcomes of apoptosis inhibiting and activation.
- •Classification.
- •4 Main types.
- •Classification.
- •16. The concept of primary and secondary alteration. Molecular mechanisms of cell injury. Lipid mechanisms role in alteration pathogenesis.
- •17. Free radicals and their role in pathological processes development.
- •19. Antioxidant mechanisms of cells. Antioxidant insufficiency.
- •19. Apoptosis and necrosis comparative characteristics.
- •20. Reactivity. Types. Dependence on sex.
- •23. Resistance. Passive and active resistance. Resistance and reactivity relationship.
- •25. Constitution, role in pathology, types classification.
- •26. Diatheses.
- •27. Stress, general adaptation syndrome.
- •28. Stress-inducing and stress-limiting systems. Diseases of adaptation.
- •29. Concept of “local microcirculatory disorders”. Some mechanisms.
- •30. Arterial hyperemia
- •2 Subtypes:
- •31. Venous hyperemia
- •32. Ishemia
- •33. Reperfusion syndrome
- •34. Stasis.
- •Variants:
- •35. Thrombosis and embolism. Thrombosis characteristics.
- •3 Main factors encouraging thrombi formation (Wirhow’s triad):
- •36. Embolism.
- •37. Embolism of pulmonary, systemic and portal circulation.
- •38. Microcirculation disorders typical forms:
- •39. Intravascular circulation disorders: rheological changings and changings of blood flow.
- •41. Microvascular tone disorders.
- •42. Extravascular disorders.
- •43. Concept of inflammation. Aethiology.
- •44. Inflammation stages, main signs and types.
- •Inflammation types (continuation).
- •45. Primary and secondary alteration.
- •46. Mediators and antimediators.
- •47. Circulatory changings during inflammation.
- •48. Fever aethiology. Pyrogens classification.
- •49. Fever stages. Fever reactions types.
- •50. Fever comparative characteristics with exogenous overheating and hyperthermia other forms.
- •50. Edemas. Classification. Oncotic and hydrostatic mechanism.
- •58. Anaemias. Erythrocytes regenerative and degenerative forms. Cells of pathological regeneration.
- •54. Anisocytosis, poikylocytosis, price-jonce’ curve movements on the right and on the left.
- •55. Blood loss.
- •56. Acute and chronic posthaemorrhagic anaemias.
- •57. Hereditary hemolytic anaemias.
- •3 Groups:
- •58. Acquired haemolytic anaemias.
- •59. Dyserythropoietic anaemias.
- •60. Aplastic and hypoplastic anaemias. Metaplastic anaemia. Myelophthysis.
- •2 Groups of factors:
- •2 Main pathogenetic mechanisms:
- •61. Cardiac arrhythmias.
- •62. Concept of arterial hypo- and hypertension.
- •63. Primary arterial hypertension.
- •2 Pathogenetical conceptions:
- •64. Secondary arterial hypertension.
- •65. Cardiac insufficiency.
- •2 Overloads types:
- •66.Heart failure myocardial form.
- •67. Coronary cirulation disorders. Reperfusion syndrome. Calcium paradox. Oxygen paradox.
- •68. Respiratory failure.
- •Probes which allow to determine one or another disorders type:
- •69. External respiratory failure. Dyspnea.
- •70. Hypoxies.
- •71. Appetite disturbance.
- •2 Main mechanisms:
- •72. Caries.
- •73. Periodontitis and parodontosis.
- •74. Hypo- and hypertonic gastric dyskinesias.
- •75. Heartburn, eructation, nausea, vomiting.
- •76. Hepatic failure. Classification. Functional hepatic tests.
- •77. Hepatic failure hepatic-vascular form.
- •78. Liver excretory function disorders. Jaundices. Liver functions
- •Proteinic exchange
- •Carbohydrates metabolism
- •Lipid metabolism
- •Pigment metabolism
- •Jaundices differentiated diagnosis
- •79. Haemolytic jaundice.
- •80. Hepato-cellular or parenchymatous jaundice.
- •81. Hepato-portal hypertension. Ascitis.
- •82. Urine amount qualitative and quantitative changings.
- •Urine relative density (weight) (in morning portion)
- •83. Urine pathological components. Protein
- •Leucocytes:
- •Cylinders
- •84. Proteinuria.
- •85. Renal acid-alkaline balance disorders
- •86. Adrenal glands pathology. Cortex acute and chronic insuffieiency.
- •87. Thyroid hypofunction.
- •88. Hypothyroidism.
- •89. General regularities in occurrence and development cns disorders. Pathological processes classification.
- •90. Pathological excitement and inhibiting in nervous centers.
- •I. Of pathological excitement:
- •II. Of pathological inhibiting:
- •91. Ephaptic effects.
- •92. Pain.
Leucocytes:
under normal conditions in males – 0-2 in a vision field, in females – 1-3 in a vision field.
Leucocyturia:
nephrites:
pyelonephritis;
intersticial nephritis;
lupus nephritis;
kidneys tuberculosis;
glomerulonephritis (lymphocyturia);
cystitis;
urethritis;
pyelitis;
5) prostatitis;
6) nephrosis;
7) nephroscleroses;
8) fever;
9) intensive physical loading;
10) toxic substances action:
ampycilline;
canamycine;
aspirine;
levodopa;
heroine;
iron salts.
Leucocyturia – state when leucocytes amount in urine is more than 5-6 in a vision field. It is a feature of practically all kidney and urinary ways diseases. If such amount is more than 60 one can tell about pyuria.
Probe with 2 glasses:
Leucocyturia in the first portion (pyuria initialis) – urethritis, prostatitis; in the second one – cystitis, pyelitis, nephritis.
Probe with 3 glasses:
After prostate massage, after third portion taking (pyuria terminalis) – prostatitis.
Prednisolone probe
(for hidden leucocyturia detection)
First urine portion should be investigated in the morning, then the patient must have intravenous injection with 30 mg of prednisolone on 10 ml of physiological solution. Then 3 urine portions with 1-houred interval should be investigated. At a hidden urinary infection leucocyturia must be increased twice and more.
Cylinders
They are absent under normal conditions.
Cylinders – proteinic formations which are absent in urine of a healthy person. They are formed in nephron channels and have cylindric shape (they repeat channel´s shape).
Types:
hyalinic;
granular;
ceraceous (wax-like).
If their origin is out of any doubt – leucocytic, erythrocytic and epithelial.
Hyalinic (increasing) –
all kidney diseases accompanied by glomerular proteinuria:
glomerulonephritis;
infectious agents action;
allergic stimuli influence;
hypertonic disease;
heart activity decompensation;
acute pyelonephritis;
nephropathy of the pregnant;
kidneys new-formations;
kidneys and urinary ways tuberculosis;
fever;
intoxication with hard metals;
treatment with diuretics;
physiological:
intensive physical loading;
activity in a hot climate;
after swimming in a cold water
Granular (increasing):
active glomerulonephritis;
diabetic nephropathy;
pyelonephritis;
amyloidosis;
malignant hypertension;
intoxication with hard metals;
fever;
intensive physical loading.
Wax-like (increasing):
renal insufficiency;
amyloidosis.
Leucocytic (increasing):
pyelonephritis;
lupus-nephrits.
Erythrocytic (increasing):
glomerulonephritis;
kidney infarction;
renal vein thrombosis;
malignant hypertension;
subacute bacterial endocarditis;
polyarteriitis;
Epithelial (increasing):
renal channels acute nephrosis;
viral diseases;
amyloidosis;
intoxications with hard metals;
salicylates action;
ethylenglycol action.
84. Proteinuria.
Selected – when low-molecular proteins are appeared in urin.
Non-selective – both low- and highly-molecular proteins can be in urine.
By selectivity degree pathophysiologists can tell about:
nephrotic proteinuria – albumines or albumines+globulines are in urine;
nephritic – all plasma proteins are in urine – albumines, alpha-, beta, gamma-globulines.
At increased protein content in urine one can tell about proteinuria which on its developmental mechanism can be:
physiological:
orthostatic (at long-termed standing);
overcooling;
after long-termed physical training (especially running on big distance);
at work in high-temperature regimen;
glomerular (delt with kidney glomerules increased permeability:
glomerulonephritis;
infections;
allergy;
hypertonic disease;
heart activity decompensation.
High-molecular proteins detection testifies to kidney filter selectiveness absence and its expressed injure.
channel or tubular (connected with channels incapability to reabsorb proteins which have passed through intact glomerular filter:
amyloidosis;
acute channel necrosis;
intersticial nephritis;
Fanconi syndrome (hereditary tubulopathy).
prerenal (delt with tissular proteins enforced decomposition, at low-weight proteins such as Benz-Jons´, myoglobine, haemoglobine increased level in plasma:
myelomic disease (Benz-Jons´ protein);
muscular tissue necrosis;
erythrocytes haemolysis.
postrenal (at urinary ways and sexual organs pathology):
cystitis;
urethritis;
colpitis et al.
Glomerular and channel forms are often united in renal proteinuria.
