Place and role of the pathology in the medicine. Structure ...€¦ · Structure of pathology and...
Transcript of Place and role of the pathology in the medicine. Structure ...€¦ · Structure of pathology and...
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Place and role of the pathology in the medicine.
Structure of pathology and methods of investigation
Dr. Attila Zalatnai
(Just for educational purposes)
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Without pathology there is no modern diagnostics!
Law: „all surgically removed tissue must be sent to pathology!”
routine: 8 % formalin
other studies: 0,9 % NaCl
never should be dry!
Except: tooth
normal placenta
nail
eye lens
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PARTS OF THE PATHOLOGY
Autopsy:
- obligatory in Hungary
- autopsy report - must be archived
- clinician must be present
Histopathology:
- it determines the therapeutic strategy
(gold standard)
- resection, excision, core biopsy
- intraoperative frozen section
- histopathological report - must be archived
Cytology:
- exfoliatíve cytology (e.g. fluids)
- abrasive cytology (cervix, bronchus, stomach)
- fine needle aspiration cytology (FNAB, FNAC, ABC)
Molecular pathology:
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Autopsy
- controls the clinical diagnoses (quality control)
- provides epidemiological data
- characterization of newly discovereddiseases
- better understanding of the naturalhistory of malignant diseases
- recognition of the morphologicalalterations (medical teaching)
- exclusion of forensic cases
- defense against the malpractice charges
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Histopathology
Determines the treatment strategies!
abscess forming inflammation antibacterial treatment
tbc specific antituberculotic treatment
metastasis search for primary neoplasm
removal of the whole organ
decides the extent of operation
staging of the malignant tumors
primary malignant lymph node tumor
chemotherapy
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- characterization of the effusions
- screening for preneoplastic conditions
- recognition of the nature of focal lesions
(breast, thyroid, liver, salivary gland, brain…)
Cytology
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Normal tissue
Abnormal noxas
degeneration adaptation
hyperplasia
hypertrophy
hyperplasia + hypertrophy
necrosis
death
superinfection
tissue loss
mutilation
resorption
cavitation
fistule
pseudocyst
Reparation
fibrosis
scarring
calcification
ossification
metaplasia
inflamm. atrophy
pseudometaplasia
pseudo-hypertrophy
regeneration
dysplasia
malignant transformation
((
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Degenerations (dystrophies)
Results of metabolic cellular damage, morphological apprearances of the intracellulardisturbances
Many different causes – nonspecific!
- tissue hypoxia, shift in pH
- intracellular ionic imbalance
- toxic damage
- distant effect of severe generalized inflammations
- burn, freezing
- intoxications
- Parenchymatous degeneration (cloudy swelling)
- Hydropic degeneration
- Vacuolic degeneration
- Fatty degeneration
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Parenchymatous degeneration(cloudy swelling)
Impaired intracellular oxidation
Inefficient K/Na-pump
Increased membrane permeability
Increased intracellular water content
Parenchymatous organs (heart, liver, kidney)
Swollen, wet, pale brown, friable
Granular cytoplams
(swollen organelles)
Kidney: dilated stellate veins
Tubular lumens: virtual, narrow
Hydropic and vacuolic degeneration
More severe cellular damage
Cytoplasmic water accumulation
Hypertonic solutions
Intoxications (coolant; ethyleneglycol)
Hypokalemic conditions
(e.g. Conn-syndrome)
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Fatty degeneration
Accumulation of neutral lipids (triglicerides) in the cytoplasm
Depending on the size of lipid droplets: microvesicular – macrovesicular
Increased trigliceride-synthesis Impraired trigliceride-excretion
- hyperlipidemias - impaired protein synthesis
- increased fatty acid synthesis - alcoholism
- decreased fatty acid oxidation (disturbed membrane transport)
(hypoxia, acidosis) - shortage of lipotropic materials
Characteristic localizations: LIVER, heart (diffuse, or „tiger heart”), kidney
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Glycogen storage
• Genetic disorders resulted from enzmye deficiency or defect (gene mutations )
• Autosomal recessive (rarely: sex-linked) inheritance
- manifested in homozygotics, heterozygotics are carriers –
• Manifested mainly in neonatal period or in childhood
I. (von) Gierke’s disease (hepatorenal glycogenosis)
II. II. Pompe disease
III. III. Cori disease
IV. Andersen disease
V. McArdle disease
PAS
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Pigments
Exogeneous Endogeneous
Coal dust (anthracosis) Lipofuscin
Tattoo (incl. amalgam-tattoo) Hemosiderin
Melanin
Bilirubin (jaundice, icterus)
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Nevus forms
1. Intraepidermal (junctional) -
2. Intradermal -
3. Compound –
4. Blue –
5. Spitz (spindle cell) –
6. Congenital giant –
7. Dysplastic nevus syndrome
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