sam kyle Flashcards
Agenesis
-> Absence of Anlage( primordial tissue)
Aplasia ( one P )
->Anlage Present, but doesn’t develop
Hypoplasia ( 2x Ps)
- > Partially present
- > Histologically normal
Atresia
-> Incomplete formation of lumen ( TRUNK)
Necrosis
-Death of cells + Inflammatory infiltrate
1) Cytoplasm
- Increase eosinophilia ( Loss of cytoplasmic RNA)
- Vacuolated cytoplasm ( digested organelles)
- Myelin figures ( Damaged cell membranes)
2) Nuclei
- Karyolysis ( loss of chromatin basophilia)
- Pyknosis ( nuclear shrinkage)
- Karyorrhexis ( fragmentation)
COAGULATIVE necrosis
- -> “Architecture” is preserved
- -> NECROTIC cells removed by phagocytosis
- Can be pale( No haemorrhage) or red ( loose tissue with RBC)
LIQUEFACTIVE necrosis
- -> transformation into liquid viscous mass
- -CNS
- Infection ( pus)
GANGRENOUS necrosis
- LACK of blood supply
- -> “Crosses multiple tissue planes”
CASEOUS necrosis
- White ( cheese-like)
* -> TB ( granulomas)
- White ( cheese-like)
FAT necrosis
-> release of pancreatic lipases by pancreas into perioneum
FIBRINOID necrosis
-antigen-antibody complexes deposit in walls of arteries-> mixes with fibrin to form pink and amorphous “fibrinoid” appearance
- -> Rheumtoid nodules ( epithelioid histiocytes + lymphocytes and plasma cells)
- -> Aschoff bodies ( rheumatic fever) - found in myocardium
Neoplasia (New growth)
- Abnormal mass of tissue with autonomous growth exceeding normal tissues
- Persists after stimulus is withdrawn
- > Benign: Cannot metastasize
- > Malignant: Invade and destroy adjacent structures
HAMARTOMA
-> Overgrowth of cells INDIGENOUS to site
SITES
- Lung
- Breast
- -Hypothalamus
- heart ( rhabdomyoma)
- brain
SYNDROMES
- Cowdens( multiple hamartoma syndrome)
- Tuberous sclerosis
- Peutz-Jegher ( GI)
CHORISTOMA
-> Ectopic normal cells
TERATOMA
-Differentiation along
- -> MESODERMAL
- -> ENDODERMAL
- -> ECTODERMAL
TYPES
1) Mature= DERMOID cyst
2) Immature ( MALIGNANT)
3) Monodermal ( highly specialised)