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105 Cards in this Set

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Severely ill pt. in shock developes Azotemia and Oliguria what would biopsy reveal
Acute tubular necrosis
#1 reason for pre renal shock and acute renal failure, results from ischemia or toxic injury
Subepithelial Humps, PMN present,sore throat for 14 days earlier, periorbital edema
Acute post streptococcal glomerulinephritis
Fever rash, eosiniphils, after course of METHACILLIN
acute interstitial pephritis
renal stone developed from Urea spiltting organis
Triple phosphate AKA- Struvite
Calcium Oxalate forms stone 75%
Infant, autosomal dominant, abdominal girth, abdominal pain, moderate hypertention, reduces liver funtion. pt. dies while waiting for evaluation by massive intracranial hemorrhage
autosomal dominant infant polycystic kidney disease
most common renal cell carcinoma (tumor)
Clear cell carcinoma-
painless hematuria
chromosome 3
flank pain
highly PIGMENTED history of bronchitis and many bullae
Centriacinar
alpha 1- antitrypsin
Panacinar emphaysema
pt. presents with asthma, what cell is likely to be increased
eosinophils, (associated with mast cells, IgE)
5 year old child aspirates a peanut resulting in atelectasis is called
Abstructive/absorptive
cavitary disease @ the apex of the lung
Secondary TB (granulomatous, reactivation, reinfection)
subplueral parenchymal nodule w associated lyph node involvement
primary TB (GHON complex, mid lung first exposure)
Most common Lobar pnuemonia
Strep, diffuse has 4 stages1-congestion
2- red hepatization
3- Gray hepatization
4 resolution
second type (Bronchial- patchy, Stap
4 stages of Lobar pnuemonia
CRGR
Congestion
Red Hepatization
Grey Hepatization
Resolution
Type II sensitivity reaction inclused
Transfusion rx.
Hemolytic deases of newborn
Good pasture
Graves disease
Myasthenia Gravis
Type I Hypersensitivy rx includes
Asthma
Hayfever
Laryngeal Edema
IgE,
Eosinophila
Mast Cells
Histamine
Seratonin
Type I delayed phase
Lukotrienes Prostoglandins
what mediates type I sensitivity
Mast cells
Type III hypersensitivity is called what and acts systemically and locally
Immune complex
Systemic-Serum Sickness
Local-Arthrus reaction
Type III examples
Snake bite- antivenom
Lupus
rheumatoid arthitis
Type III does what to complement serum levels
It would decrease complement serum level in the blood vessel wall
Anti smith antibody is present in
SLE(lupus)
maclopapular eruption
Aids pt. has abdominal pains and Acid-fast stool what the most likely cause of pt.s diarrhea
Cryptosporidium
CD4 recognizes antigen on
MHC II molecules
Type I hypersensitivy characterized by
Mast cells and IgE
TB tuberculin test is type _ hypersensitivity
Type IV delayed hypersensitivity
Pt. presents with blurred vision and positive for SS-B antibodies and history of rheumatois arthritis
Sjogrens syndrome
Xerostomia
associated with Lyphomas
Pt. presents with fatigue weight loss, admits to being an IV drug user what test should be administeres
ELISA to look for antibodies then western blot to confirm particles, want to look @ Viral load
Antibodies are produced by
Plasma cells and plasma cells are produced by B-cells
Pt. presents w weaknes weight loss, arrythmias, protruding tongue, positive CONGO RED stain the next appropriate stage would be to
look @ serum stain under polarized light -Green apple
Amyloidosis
which hypersensitivity result in vaculities
Type III Immune compleyx because it act on vascular wall- also cause fibrinoid necrosis
Cross Beta pleated sheets
"Bence Jones"
Over 50
Use Congo Red and flourescent light to dx.
Amyloidosis- associated with Alziehmers and Endocrine disease
Acute Respiratory Distress syndrome can be caused by
Pancreatitis
Shock
Sepsis
Pulmonary Thromboembolism
Acute and large-Saddle embolism
Medium- block pulmonary=RBC escaping
block bronchial=infarct-#1 chronic left sided heart disease
Small thrombus-Cor Pulmonale- hypertrophy of right heart
#1 tumor of the lung
Metastatic
Bronchogenic tumors include
Squamos cell
Adenocarcinoma
Small Cell Carcinoma
Large cell carcinimo
Whats the most aggressive Bronchogenic tumor
Small cell"OAT" cell carcinoma
Pulmonary TB has 2 types
Primary- Ghon Complex- mid lung field
Secondary- reinfection/reactivation- Apex cavity type IV hypersensitivity
most common Primary Atypical pnuemonia
Mycoplasm Pneumoniae- Interstitial confinement
common in children
accumulatiuons in alveolar wall
Lung abcess is due to what bacteria
Staph A. pyogenic
Right lung usaully affected
Alcohol or drug overdose
bronchial obstruction
Atelectasis by congenital means is due to
Hyaline membrane disease or prematurity
Aquired Atelectasis can be either
Abstructive/absoptive- by means of and obstruction- lung will shift towards collapsed lung
Compression- due to trauma or external pressure i.e. hydrothorax- mediastinum will shift awat from collapsed lung
Acute atalectasis is usaully due to
post-op complications
Pulmonary edema can be caused by
Left ventricular failure
shock leading to incrasesed capillary permeability or rapid ascent to high altitudes
Bronchiogenis cyst
usually in area of suprasternal notch
lined by respiratory epithelial
has cilia
Pulmonary sequestration is usaully complicating due to
infection- cystic lung disease
Bronchietctasis is?
it may lead to
permanent abnormal dilitation of bronchials caused by chronis infection
May lead to lung abcess and COR PULMONALE
Bronciectasis is often seen in pt's with
Kartagener disease-
Serile
situ inversus
sinusitis
Emphysema is
permanent dilitation and destruction- lack of elastic recoil
Emphysema usually caused by smoking and assiciated with pigmentation
Centilobar- terminal bronchiole(APICAL) usually caused by smoking
emphysema associated with a genetic defieciency in alpha 1 antitrypsin
Panacinar
emphysema associated with distal part of acina
Paraseptal or DISTAL
there is also an Irregular emphysema- assocated with scar tissue
Chronic bronchitis is defined by
have a chronis cough for 3 months for 2 consecutive years- hypertrophy of mucus glands- can lead to cor pulmonale
clearly linked to SMOKING
COPD Chronic obstrutive pulmonar disease is characterized by
Obstruction of airflow
Bronchial asthma is characterized by in increase in this antibodies and have these associated with them
Ige and MAST cell
Curshman spirals
charlot leden crystals
smooth muscle hypertrophy
Acute pyelonephritis is what type of infection usaully caused by
Bacterial- Neutreutrophils WBC
ECOLI
obstruction and instrumentation
In Acute pyelonephitis you will find this in urine
WBC cast
Acute pyelonephritis can lead ultimately to chronic pyelonephritis which causes
chronic renal failure
Chronic*scarred kidney and dialated blunted calyces
Drug induced interstitial nephitis ultimately causes
The drugs usually involves
chronic*Papillary necrosis
Methecillin, nsaids
type I hypersensitivity(eosinophils)
chronic anelgesic abuse
Chronic interstitial nephritis is due to
Analgesic nephropathy
Acute tubular necrosis is the most common cause of
#1 cause of ACUTE Renal Failure
Acute tubular necrosis is usaully due to
Shock or toxic injury
ex:antifreeze, aminglycosides
usually ends in acute renal failure
Acute tubular necrosis usaully requires
Dialysis

epithelial cell necrosis and sloughing off evidence of regeneration
proximal tubule usually affected
Vascular Hypertension cause is usually
Idopathic
Vascular Hypertension usaully causes
diastolic higher than 120
Benign Nephrosclerosis
benign Nephrosclerosis usaully presents as having this appearance
Onion skin an Hyaline thickening
Vascular hypertention can cause a fast acute change called
Malignant Nephosclerosis which is a medical emergency
causing petechial hemorrhage
again onion skin appearance
Adult renal polycystic kidneys are autosomal dominant and cause
enlarged kidney
hematuria
Flank Pain
Infant polycystic kidney will have this appearance
smooth and can cause compression of lungs and other organs as they are enlarged
Nepholithiasis(Stones) are two types
Calcium Oxalate or Struvite aka; triple phosphate
Nephrolithiasis are due to high concentration of
Cacium 90%- stone will cause obstruction which leads to hydronephrosis which causes dialation of calyces and the medulla will thin out
Hydornephrosis is causes by
Foreign bodies, nephrolithiasis(stones) which will cause dialation of the calyces
Renal cell carcinoma most common type is-
and is also known as
Clear cell, silent hematuria or ADENOCARCINOMA
mutation with chromosome #3
usually in the upper pole
Renal cell carcinoma also cause
Paraneoplastic syndrome
Wilms tumor is most common tumor in
Children- usaully an abdominal mass found by Dr.
Prognosis of Wilms tumor with surgery and radaition therapy?
good prognosis
Carcinoma of the urinary bladder usually affect what type of cells
transition cell carcinoma has a four scale grading- I-4 cells thick
2-7 cell thick
3-10 cell thick
4- Anaplastic(disarrayed)
Cacinoma of the bladder is usaully measured in its invasion of
the muscular layer
Mahler
Developed 6-stage theory that describes the process of separation and individuation: normal infantile autism; symbiosis; differentiation; practicing; rapprochement; object constancy. Separation is becoming a discrete physical entity by physically distancing.
The hallmark of acute glomeruli nephritis is
RBC cast in urine
Hallmark of acute pyelonephritis is
WBC cast
Nephrotic syndrome is due to
Leaky basement membrane and foot process destruction
Nephrotic syndrome usaull presents as
Heavy proteinuria
Hyperlipidemia
Lipiduria
Edema
GRF is normal
Nephritic syndrome usaully presents as
Obstruction of glomeruli wall, this blockage causes damage to wall and you will see rbc in urine(hematuria) increase BP due to RENIN and decrease GFR which increases BUN and creatinin levels
With nephritic syndrome you see what type of edema
Periorbital
Renal tubular defect manifest as
Nocturia and polyuria
metabolic acidosis
Pre-renal causes of Acute renal failure are
Shock
-hypovolemic
-septic
-cardiogenic
Renal causes of Acute renal failure
Severe Nephritis
malignant hypertension
Post renal causes of acute renal failure
Stone
Chronic renal failure is characterized by a GFR
@ or less than 25 ml/min
Uremia
Glomeruli diseases that deposit Ag-Ab complexes in the glomerulus wall are type--- hypersensitivity
type III
Injury to the glomerulus by anitbodies reactin in situ are type---hypersensitivity
type II
Diseases causing Nephrotic syndrome
Minimal change
Membraneous proliferative
Membranous glomeruli nephritis
Focal segment glomeruliscerosis
IgA nephropathy
SLE
A
Diseases cause by Nephritic syndrome
V
Post streptococcal GN
Rapidly progressive cresentic
IgA
Membranoproliferative
SLE
Minimal change is usaully in children and treatment prognosis is usaully
good with steroid tx.
Membranous glomerulonephropathy is in adult and a result of
Immune complex deposits in BM
causes "Spikes and domes"
although it nephotis you see hematuria and hypertension
Focal segment sclerosis is usaully due to
Heroin and HIV and AIDS
incease in IgM antibodies
Membranoproliferative glomerulinephritis presents as a decrease in
C3, hypocomplement, charaterized by mesangial and endothelial cell proliferation
Membranoproliferative has two types(aka mesanigoproliferative)
1- Subendothelial deposits in basement membrane
2-Dense ribbon like deposit renal failure in ten years TYPE 2 worst
membranoproliferative can have this type of appearance
Train track- due to splittin of BM
Acute post streptococcal GN is a nephritic syndrom and presents with
lumpy bumpy deposits it is a
Immune complex disease- type III
Rapidly progressin cresentic GN is usaully deposited in this form
linear and found in good pastures disease
Very poor prognosis
Rapidly progressing cresentic GN has 3 types
1-good pastures- usaully need kidney transplant
2-immune complex
3-wegners - PANCA
IgA nephropathy (Bergers Disease) characteristic presentation is
Mesangial proliferation
usaully in young men
Chronic glomerulinephritis is the
"END" stage of many glomeruli diseases
#1- Rapidly progressing GN
#2-Focal Segmental
#3-membranpproliferative
#4-Iga
#5-membranous
#6- Post-Step