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General pathology lecture 1 introduction & cell injury


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Dr. Barcarse

General pathology lecture 1 introduction & cell injury

  1. 1. INTRODUCTION and CELL INJURY Lecture 1
  2. 2. Medicine, to produce health must study diseaseAnd music, to produce harmony must study discord. by Plutarch
  4. 4. Definition of Pathology It is the “scientific study of disease“. "scientific study of the molecular, cellular, tissue, or organ system response to injurious agents."Pathology serves as a "bridge" or "link" between the preclinicalsciences (anatomy, physiology, ……etc.) and the courses in clinical
  5. 5. What is the Disease?• It is the “state in which an individual exhibits an anatomical, physiological, or biochemical deviation from the normal”.
  6. 6. Basic Language of Pathology In order for a subject or course to bemeaningful, one should become familiarwith the basic terminology applicable to
  7. 7. Learning Pathology:• General Pathology – Common changes in all tissues. e.g.. Inflammation, cancer, ageing, edema, hemorrhage ….etc.• Systemic Pathology – Discussing the pathologic mechanisms in relation to various organ systems e.g. CVS, CNS, GIT…..etc.
  8. 8. What should we know about a Disease?• Definition.• Epidemiology – Where & When.• Etiology – What is the cause? gy• Pathogenesis - Evolution of dis. th o lo Pa• Morphology - Structural Changes• Functional consequences• Management• Prognosis• Prevention
  9. 9. Pathology focuses on 4 aspects of disease: ETIOLOGY: Cause of disease. PATHOGENESIS: Mechanisms of development of disease. MORPHOLOGY: The structural alterations induced in cell and tissues.
  10. 10. Manifestations of DiseasesThe manifestations of a disease are the sum of the damage done by a harmful agent and the body’s response.The variation in these components accounts for the great diversity of disease, which can be classified into 4 main groups:1. Developmental – genetic, congenital2. Inflammatory - trauma, infection, immune3. Neoplastic - tumors, cancers4. Degenerative – ageing5. Iatrogenic – drug-induced
  11. 11. Manifestations of Diseases• Signs – are objective findings as perceived by an examiner, physician or dentist• Symptoms – are functional manifestations or evidences of a disease process• Lesions – are visible changes produced by a disease in the tissues or organs. They are usually local abnormalities which could be benign, cancerous, gross, occult, or primary.• Exacerbations – a sudden increase in the severity or seriousness of the signs and symptoms during the course of a disease.• Remissions – become less intense at a time.• Complications – unfavorable conditions that arise during the course of a disease• Sequelae – are remote aftereffects produced by a disease.
  12. 12. ETIOLOGYKnowledge or discovery of the primary etiology remains the backbone on which a diagnosis can be made and a disease process can be best understood so that a treatment can be prescribed.THE ETIOLOGICAL FACTORS ARE: - ENVIRONMENTAL FACTORS - GENETIC FACTORS - IINDIRECT CAUSESENVIRONMENTAL FACTORS ARE: - PHYSICAL AGENTS – radiation, trauma or mechanical injury, thermal changes, electrical, nuclear or X-rays, changes in atmospheric pressure - CHEMICAL AGENTS – chemicals, poisons like venoms or toxins, corrosive agents like strong acids and alkalis -NUTRITIONAL DEFICIENCES AND EXCESSES - INFECTIONS AND INFESTATIONS - ABNORMAL IMMUNOLOGICAL REACTIONS - PSYCHOLOGICAL FACTORSGENETIC FACTORS: ABNORMAL GENESINDIRECT CAUSES: pertain to the predisposing factors like age, age, sex, environment, race, climate, state of nutrition, habits
  13. 13. Etiology Disease Disease Disease Disease DiseaseOne etiologic agent •One etiologic- one disease, as •Several etiologic agents agent severalMalaria. one disease, as diseases, as diabetes . smoking.
  14. 14. Etiology: What is the cause? Environmental agents: • Physical • Chemical • Nutritional Multifactorial: • Infections As Diabetes, • Immunological • Psychological Hypertension Genetic Factors: Cancer • Age • Genes
  15. 15. PathogenesisThe sequence events in the response of thecells or tissues to the etiologic agent, from theinitial stimulus to the ultimate expression of thedisease,”from the time it is initiated to its finalconclusion in recovery or death” The core of the science of pathology — the study the
  17. 17. Necropsy: Gross examination of the animal cadaver by systematic dissection in order to evaluate any abnormal changes (lesions) that may be present.Autopsy: Synonymous to necropsy in human medicineBiopsy: Removal and examination of tissue
  18. 18. Types of Diseases• Acute – characterized by a sudden onset or in a rapid course• Fulminating – an acute fatal disease• Chronic – slow onset and long duration or having a long course• Intercurrent – occurs during the course of another disease• Idiopathic – disease with unknown cause• Teratogenic – diseases that are cause by drugs that cross the placental barrier and harm the fetus• Contagious – transmitted by direct, intimate or by skin contact• Venereal – transmitted by sexual contact• Infectious – are caused by pathogenic microorganisms• Communicable – are transmitted by agents, fomites, vector or carrier
  19. 19. Prognosis Expected outcome of thedisease; it is the cliniciansestimate of the severity andpossible result/s of a disease.
  20. 20. CELL INJURY
  21. 21. What is cell injury?• Cell injury is a sequence of events that occur if the limits of adaptive capability are exceeded or no adaptive response is possible.• Most common causes are: ischemia, hypoxia, chemical injury, and injury produced by infectious agents
  22. 22. Overview Normal + Stress Adapted cell Cell - StressInjury +StressReversibly - Stressinjured cellIrreversibly Apoptosis Dead cellInjured cell Necrosis
  23. 23. The Normal Cell
  24. 24. Mechanisms of Cell Injury• Depletion of ATP• Mitochondrial Damage• Influx of Intracellular Calcium and Loss of Calcium Homeostasis• Accumulation of Oxygen-Derived free radical (Oxidative stress)• Defects in Membrane Permeability
  25. 25. Ischemic Injury
  26. 26. Mechanisms of Cell InjuryIschemic injury
  27. 27. Cell injury and death• Reversible hypoxic/ ischemic injury Loss of ATP generation by mitochondria initially results in reversible events: o Na+/K+ ATPase membrane pump leads to a loss of ionic and osmotic gradient ( ↑edCa+2+ Na+, ↓ed K+ and osmotic gain of water) resulting cell swelling & ER dilatation) o ↑ed anaerobic glycolysis results in glycogen depletion and lactate accumulation (↓ed pH). o Reduced protein synthesis due to ribosome detachment from the RER
  28. 28. Morphology of Cell Injury and Necrosis• Cell Injury – Reversible – Irreversible• Cell Death – Necrosis – Apoptosis
  29. 29. Cell Injury and Death• Reversible Injury o Cell swelling develops when cells are incapable of fluid an ion homeostasis (↓ed function of ATP dependant pumps). o Fatty change the accumulation of lipid vacuoles in the cytoplasm.• Irreversible injury (Necrosis) o Two basic processes underlie the morphologic changes of necrosis  Denaturation of protein  Enzymatic digestion of cell components
  30. 30. Morphology of Cell InjuryReversible Injury Cellular swelling Fatty change• Plasma membrane alteration• Mitochondrial Changes• Dilation of Endoplasmic reticulum• Nuclear Alteration
  31. 31. Morphology of Cell InjuryUltrastructural Changes:• Alteration in plasma membrane reflecting disturbance in ion and volume regulation induced by loss of ATP• Mitochondrial changes• Endoplasmic reticulum changes• Changes in the lysosomes
  32. 32. Alteration in the Plasma Membrane • Cellular swelling • Formation of cytoplasmic blebs • Blunting and distortion of microvilli • Creation of myelin figures • Deterioration and loosening of intercellular attachments
  33. 33. Mitochondrial Changes • Early, appears condensed as a result of loss of matrix protein following loss of ATP • Followed by swelling due to ionic shifts • Amorphous densities which correlate with the onset of irreversibility • Finally, rupture of membrane followed by progressing increased calcification
  34. 34. Endoplasmic reticulum changes • Dilatation • Detachment of ribosomes and disaggregation of polysomes with decreased protein synthesis • Progressive fragmentation and formation of intracellular aggregates of myelin figures
  35. 35. Changes in the Lysosomes• Generally appear late• Swelling rupture disappear• some fused with the autohagic vacuoles (phagosomes) which become apparent within damaged cells
  36. 36. Cell Injury and DeathIrreversible hypoxic/ ischemic injury • These changes are reversible if O2 and flow are reinstated, the transition to irreversible injury depends on the extent of ATP depletion and membrane dysfunction especially of mitochondria. • ATP depletion results in MPT with loss of the H+ gradient • ATP depletion releases cytochrome c that can induce apoptosis • ↑edCa+2 activates o membrane phospholipases with resulting membrane damage o Intracellular proteases leading to cytoskeletal degradation • Phospholipid degradation products that accumulate are directly toxic to the cell
  37. 37. Cell Injury and DeathIrreversible hypoxic/ ischemic injury • These changes are reversible if O2 and flow are reinstated, the transition to irreversible injury depends on the extent of ATP depletion and membrane dysfunction especially of mitochondria. • ATP depletion results with loss of the H+ gradient • ATP depletion releases cytochrome c that can induce apoptosis • ↑Ca+2 activates o membrane phospholipases with resulting membrane damage o Intracellular proteases leading to cytoskeletal degradation • Phospholipid degradation products that accumulate are directly toxic to the cell
  38. 38. Types of Cell Injury2.Cloudy or cellular swelling or parenchymatous degeneration3.Hydrophic swelling4.Fatty change5.Hyaline degeneration6.Lipoidal degeneration7.Mucoid or mucinous degeneration
  39. 39. • Cloudy swelling is due to failure of the cellular sodium pump. This allows excess Na+ to enter cells and eventually increases cellular water.• Hydropic degeneration is a severe form of cloudy swelling. It occurs with hypokalemia due to vomiting or diarrhea.
  40. 40. Fatty Degeneration • Fatty degeneration or fatty metamorphosis, steatosis is the abnormal appearance of fat within parenchymal cells. • It results from hepatotoxic agents such as C2 H5OH, chloroform, CCl4, during sever infections, in prolonged anemia and in toxemia of pregnancy. • Fatty liver is due to:  inability of the liver to synthesize phospholipids  decreased lipoprotein release from hepatocytes  Increased triglyceride production
  41. 41. • Hydropic change or Vacuolar degereration.• Appears whenever cells are incapable of maintaining ionic and fluid homeostasis.• The first manifestation of almost all forms of cell injury.• Reversible injury. Gross Findings• Pallor, increased turgor, and increased in weight.
  42. 42. Micro Findings• 1. Cell swelling, cytoplasm contains coarse granules.• 2. Nucleus not affected in light microscopy..• 3. Pigmented cast, hyaline cast.D. Others:• 1. The first manifestation of cell injury and is reversible.• 2. Increasing hydration of the cell due to alteration in ion transport at cell membrane.• 3. Cause: infection, physico-chemical injury ( toxic ), ischemia
  43. 43. FATTY PHANEROSIS-LIVER• Fatty phanerosis is the unmasking of invisible fat.• Lipid accumulates in the liver cells, mainly in the form of triglycerides.
  44. 44. FATTY DEGENERATION(Wallerian degeneration)
  45. 45. Hyaline Degeneration-Liver
  47. 47. HYALINE DEGENERATION• Zenker’s waxy hyaline masses - typhoid fever; Weil’s disease or leptospirosis• Mallory bodies- nutritional cirrhosis• Russel bodies- chronic inflammation• Crooke’s hyaline bodies - Cushing’s syndrome• Councilman bodies - yellow fever; viral hepatitis
  48. 48. CUSHING’S SYNDROMECrooke’s Hyaline bodies-Liver
  49. 49. LEPTOSPIROSIS Zenker’s waxy hyaline masses-liverCausative agent: Liptospira icterohaemorrhagica
  50. 50. Mucinous Degeneration-Colon • When there is excessive amount of mucous in unusual location, it is called mucous deg. • Cancer with high degree of mucous deg are called mucinous carcinoma or the colloid carcinoma. • Two types of mucin: true mucin and paramucin
  52. 52. LIPOIDAL DEGENERATION (Cholesterol clefts)
  53. 53. • Next Meeting:• Quiz on Normal Cell & Cell Injury• Assignment: Intracellular Accumulations
  54. 54. “True wisdom is in leaning On Jesus Christ our Lord True wisdom is in trusting His own life-giving Word, True wisdom is in living Near Jesus everyday True wisdom is in walkingWhere He shall lead the way!” Author Unknown