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General Pathology Part 2 Revised Study Guide Review
Typology: Study Guides, Projects, Research
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by penetrating/damaging epithelium. Virulence is how it adheres, invades, and delivers toxins
causes pathogen to enter) GI (food/drink contaminates) Respiratory (Inhaling bacteria/virus/fungi) Urogenital (distance from bladder to skin depends on more UTIs) Vertical Transmission (mom to newborn)
like LPS in the cell wall of gram - bacterial. Exotoxins are toxins that are secreted to hurt, like enzymes, proteins, superantigens
Mononuclear and granulomatous inflammation Cytopathic-cytoproliferative reaction (viruses) tissue necrosis chronic inflammation and scarring
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poliovirus west nil viral hemorrhagic fever
that is transmitted through respiratory track, and the patient gets a blotchy red-brown rash on the fact, trunk, and extremeties- : Measles
swelling "bump" of gland rhymes with mumps)
neuroinvasive
chicken pox latent- herpes zoster/shingles These both infect the mucous membrane
progenitors and has giant cells
4 / 16 transmitted via flea bites, on rats. See buboes- white pustules due to bacteria in the lymphatics
Causes pulmonary disease, especially in high risk people like those with HIV. There are two types- primary and secondary. Primary TB has the "ghon complex" where there is granulomas (giant cells, with central area of caseous necrosis, mononuclear inflammatory cells)
primary TB- this is an area of inflammation with central necrosis (caseous necrosis) that has giant multinucleate cells
Treponema pallidum, a spirochete. Syphilis is a chronic STD that has 3 different phases.
penis/scrotum/vulva/cervix Secondary syphilis- rash on palms, lymphadenopathy Tertiary syphilis- Neurosyphilis, Aortitis, and Gummas
skin, and mucous membrane. These are seen in people with tertiary syphilis, caused by treponema pallidum, a spirochete
localized or disseminated and has a tendency to cause chronic arthritis: Lyme disease
5 / 16 flora that live on your skin, not by a specific pathogen that you picked up somewhere
C. perfringens C. tetani C. botulinum C. dificil: C. perfringens causes gas gangrene C. tetani causes tetnus that is transmitted by puncture wounds of rusty metals, etc C. botulinum- causes botulism, caused by canned foods and releases a neurotoxin C. dificil- a GI infection that causes pseudomembranous colitis
aspergillosis and zygomycosis Yeasts are cells/chains, round and oval and budding, and examples are Candida
infections?: Parasitic, protozoa infections
RBCs. People with Sickle Cell are protected from this disease.: Malaria
membranes, or viscera. There are New World/Old World versions of this: Leishmaniasis
: African Trypanosomiasis, caused by bite of Tsetse flies, and causes parasitic proliferation in the blood that can cause brain dysfunction, cachexia, and death
7 / 16 ulcers
stimulation. It can cause heart issues and seizures: Co- caine
euphoria, and sedations. These can also cause sudden death and injure many organs: Opiates
euphoria followed by a "crash". It causes confusion and psychotic features: methamphetamines
coordination, but clears in 4-5 hours. It increases heart rate and BP and effects respiratory system as well: marijuana
when one of the 3 macros are missing or all. Secondary malnutrition is due to an issue with storing, absorbing or losing the nutrients
growth retardation and muscle loss. Their extremities are emaciated, their head looks too large, and they have a general deficiency of ALL nutrients.: Marasmus
macros. The [child] usually is on an only-carb diet, usually in a poor country/area. They have a big belly and skinny body, with skin lesions, pigment changes, and hair changes: Kwashiorkor
8 / 16 regulating lipid metabolism, and involves "retinol, retinal, retinoic acid".: Vitamin A
vision, esp at night, keratinization, dry eye, squamous metaplasia Toxicity- headache, dizziness, stupor, blurred vision (similar to brain tumor), wgt loss, anorexia
plasma and helps with bone mineralization and neuro- muscular transmission.: Vitamin D
(bowed legged) and Osteomalacia in adults (soft bone) Toxicity- metastatic calcifications of soft tissues
collagen: Vitamin C
defects and bone disease. limes/lemons give source of Vit C to help. Get hemorrhages in scurvy because collagen strength in bv is low. Toxicity- rare to have toxicity of Vit C
years later
errors where there is an intrinsic abnormalities in development, where it just develops and starts out wrong. Disruptions are secondary errors of organs that were previously normal, and are due to extrinsic disturbances.
10 / 16 -deposits of hyaline in airspaces
?: Deficiency of pulmonary surfactant (by type 2 alveolar cells) (prevents lung collapse and increases SA)
blue and is obviously having issues breathing. You listen and hear what sounds like "fine rales" when they breathe, and an X-ray shows the lungs having a "ground glass" appearance. What would you diagnose the baby as having?: NRDS, or hyaline membrane disease
infections- ASCENDING- the fetus acquires by inhaling infec- tion in amniotic fluid or by passing through infected birth canal Transplacental infections- HEMATOLOGIC- parasitic and viral moreso, occurring any time in gestation; TORCH infections
growth
hydrops
11 / 16 SECOND pregnancy, the mom's anti-Rh+ Abs attack the baby's blood cells and hurt the baby.
hydrops?: Hydrops fetalis- this is caused by ANEMIA (blood cells being attacked, causes edema in baby) Kernicterus- this is caused by JAUNDICE (unconjugated bilirubin collecting in BRAIN- causing cns damage)
genetic disorders
retardation and can't walk or speak. The doctor says this is a genetic disorder- which infant genetic disorder is it?: PKU- (phenylketonuria)
is overall failing to thrive. The doctors say that this is a genetic disorder- which infant genetic disorder is it?: Galactosemia
is viscous and obstructs passages, and affects the salivary glands, pancreas, liver, vas deferens, and pulmonary tract, but does not affect sweat glands. What genetic disorder is this?: Cystic Fibrosis- issue with CFTR gene
with cystic fibrosis?: The mucous plugs these glands, causing atrophy, fibrosis, increased infections, difficulty breathing, abscesses, and even
13 / 16 childhood
and kidney
rhabdomyosarcoma, hepatoblastoma, teratoma, ependymoma, retinoblastoma, Ewing sarcoma, medulloblastoma
Found in sympathetic ganglia and adrenal medulla, and are derived from NCC
of infancy: Neuroblastoma
malignancy in the US: Wilm's Tumor
Syndrome are all risks of developing which infant tumor?- : Wilm's Tumor
omphalocele, adrenal cytomegaly, and risk for Wilm's tumor
Autosomal Recessive
and Ehlers-Danlos Syndrome
breasted and has scoliosis. What does he have, what is the genetic issue, and what are risks he
14 / 16 should be warned about?: Marfan's Syndrome Issues with Fibrillin gene, issues with connective tissue Risks- mitral valve floppiness and regurgitation, aortic dissections and cardiac failure, and dislocation of lens "ectopia lentis"
Aortic Dissection
genetic disorder due to a defect in collagen. It affects the skin, ligaments, joints. Characteristics- hyperextensible skin (fragile, stretched, vulnerable skin) and hy- permobile joints (bend thumb back, bend knee forward) Risks- RUPTURES of colon/large arteries and ocular fragility and retinal detachment
in the LDL receptor, so issues transporting and metabolizing cholesterol Characteristics- xanthomas (yellow fatty spots), atherosclerosis of major vessels, Risks of MI
Pick A, B, C Gaucher Disease
also called Gm2 gangliosidosis, and is prevalent in Jews. It involved the CNS and the retina- causing motor/mental deterioration. The hallmark is a cherry red spot in the macula: Tay-Sachs
16 / 16 infertility, lack of secondary sex characteristics: Klinefelter's Syndrome
Risk of type 2 diabetes risk of autoimmune diseases
disease on the Left side, streak ovaries, failure of secondary fe- male sex characteristics to form (breast, pubic hair), and amenorrhea: Turner's Syndrome (X)
and testicular tissue Pseudohemaphroditism- disagreement between pT and gonadal sex (ex, female pseudohempahrodites have ovaries but also have male external genitalia)
and is due to a trinucleotide repeat. What are characteristics of a child with this?: Fragile X Syndrome Characteristics- Mental retardation, long face with large mandible, large everted ears, large testicles Macro-orchidism