Pathology - Sheet1 Flashcards
Cardiogenic/Hypovolemic Shock
- Low output failure
- incr TPR
- Low cardiac output
- Cold, clammy pt (vasoconstriction)
Septic Shock
- High output failure
- low TPR, vasodilation
- High cardiac output
- Hot pt (vasodilation)
Rolling
- neutrophil: Siayl-Lewis
- endothelial: E/P Selectin
Tight binding
- neutrophil: Integrin/LFA-1
- endothelial: ICAM-1
Diapedesis
- neutrophil: PECAM-1
- endothelial: PECAM-1 (platelet enodthelial cell adhesion molecule-1)
Migration of the leukocyte, bacterial products (that attract):
C5a IL-8 LTB4 Kallikrein (CILK)
Free radicals eliminated by
Antioxidants: Vit A, C, E
Catalase, Superoxide dismutase, Glutathion peroxidase
Spnotaneous decay
Granulomatous diseases
TB, systemic fungal (histo, cocci) - caseating Syphilis (treponema pallidum/Gummas) Leprosy (M. leprae) Bartonella henselae (cat scratch) Sarcoidosis Crohns Wegners/granulomatis w polyangiitis Churg-Strauss Berylliosis, Silicosis
granuloma formation
- infected macrophage secretes IL-12 –> T cells and NK cells then secrete IFN-gamma –> activate macrophages (Janus Kinase –> STAT –> increased killing abilities), which secrete TNF-alpha –> Granuloma formation.
- anti TNFalpha meds –> granuloma breakdown and disseminated ds
Incr ESR
Infxns, cancer, SLE, inflammation, pregnancy
Decr ESR
Sickle cell (altered shape), polycythemia (too many, make it hard to fall efficiently), CHF
Iron poisoning
- -> peroxidation of membrane lipids (from formation of free radicals)
- Acute: gastric bleeding
- Chronic: metabolic acidosis (loss of bicarb in diarrhea?) scarring –> GI obstruction
Amyloidosis
- abnl aggregatino of proteins or their fragments into Beta-pleated sheet structures
- -> cell damage, apoptosis
- affected tissue has waxy appearance
- apple-green birefringence (congo red stain)
Amyloidosis: AL (primary)
Deposition of Ig Light chains (MM, plasma cell disorder)
–> Nephrotic syndrome, heart failure, arrhythmia, easy brusing, hepaomegaly, neuropathy (goes everywhere!!)
Amyloidosis: AA (secondary)
Composed of Amyloid A
- seen in chronic ds: RA, IBD, spondylarthropathy, infxns
- -> multisystem (like AL/primary)
Amyloidosis: dialysis related
- Beta2-microglobulin in pts w ESRD and long-term dialysis
- -> Carpal tunnel syndrome, other joint shit
Amyloidosis: inherited
many types
-one is: ATTR neurologic/cardiac amyloidosis from transthyretin (TTR/prealbumin) mutation
Amyloidosis: Age-related (senile) systemic
- Deposition of normal (wild-type) TTR in myocardium and other sites
- -> slower progression of heart failures vs. AL
Amylodosis to 1 organ
Alzheimers! Deposition of amyloid-B protein cleaved from APP (amyloid precursor protein)
How cancer invades –> Metastases
- invades BM using Collagenases and Hydrolases (metalloproteinases)
- “Seed and soil” theory: Seed=tumor embolus (floats around until it finds someplace to settle), Soil=target organ (specifically wants to go to X organ)
Reversible (cell changes)
- Hyperplasia - incr in number of cells
- Metaplasia - change from type A cells to type B (barrett’s!)
- Dysplasia: loss of cell orientation, shape, size; preneoplastic
Irreversible (cell changes)
- Anaplasia: abnl cells lacking differentiation)
- Neoplasia: clonal prolif of cells (uncontrolled); benign or malignant
- Desmoplasia: fibrous tissue formation in response to neoplasm
Grade and Stage
- Grade: degree of cellular differentiation
- Stage** (prognostic): degree of localization.spread baded on site of primary lesion (based on clinical or pathologic findigns: Tumor size, Node involvement, Metastases)
Carcinoma/Sarcoma
- Carcinoma: eptihelial origin. Sarcoma: mesenchymal origin
- e.g. (benign/Malignant)
- Blood vessels = Hemangioma/Angiosarcoma
- smooth m= Leiomyoma/Leiomyosarcoma
- Bone = Osteoma/Ostesarcoma
Cachexia
weight loss, muscel atrophy, fatigue
-Mediated by TNF-alpha (“Cachectin”), IFN-gamma, IL-6
Down syndrome –>
ALL, AML, Alzheimers
Xeroderma pigmentosum, Albinism –>
Melanoma, basal cell, squamous cell**
Chronic atrophic gastritis, perncious anemia, post-surgical gastric remnants –>
Gastric adenocarcinoma
Tuberous sclerosis (facial angiofibroma, seizures, MR) –>
Giant cell astrocytoma, renal angiomyolipoma, cardiac rhabdomyoma