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58 Cards in this Set

  • Front
  • Back
Normal BP
< 120/80
Pre HTN
120-139 / or 80-89
HTN Stage 1
140-159 / or 90-99
HTN Stage 2
> 160 / or 100
Hemolytic Anemia
Premature destruction / removal
Extravascular hemolysis
Thru spleen
B12
Macrocytic anemia
Scissor walk
Demyelination
Microcytic Anemia types
Thalassemia
Iron Deficiency
Aplastic Anemia
Something kills Precursor in BM
Too much RBC
Hematocrit > 42%
Hemolytic Disease of Newborn
Rhogam IgG binds to Rh antigens
WBC normal count
4-10k
Leukocytosis
High WBC count > 12k
Leukopenia
Not enough WBC count < 3k
Acute Lymphoblastic Leukemia
TdT+
Children
T or B cell precursor
Acute Myelogenous Leukemia
Adults
Aure Rods
Liquid Phase
Mouth ulcer
Chronic Lymphocytic Leukemia
Adults - die with it
Blast Crisis - 2nd hit --> acute
High WBC count - 150k
B cell
Solid
Chronic Myelocytic Leukemia
Adults
Mature cell, low LAP (cell don't work)
Blast crisis
Ph' Chromosome
Soft tissue met = choloroma
Ph Chromosome
Chromic Myelocytic Leukemia
9:22
Tyrosine kinase ON
Petichae
Low/non-working Platelet
Small ruptures ~rash
Thrombopoietin
Increases platelets
Thrombocytopenia
Low platelets
Hemophilia A
Factor 8 enzyme (can't activate 10)
Made in liver
Extrinsic Pathway
Hemophilia B
Factor 9
Intrinsic
X-mass
Von Willebrands
Factor 8 glycoprotein
autosomal dominant
Type 1 -reduced
Idiopathic Thrombocytopenia Perpera (ITP)
Autoimmune destruction of platelets
Lack TTP
stabilizing factor
platelets stick to everything
Thromboplastin
Tissue factor
activates clotting
Non-Hodgkin lymphoma
Small Lymphocytic Lymphoma
no Germinal Centers, node is over run
Liquid phase = Chronic Lymphocytic Leukemia
Solid Phase = Lymphoma in lymph nodes
Nodular pattern
Burkitt's Lymphoma
American - Retroperitoneal

African - jaw, EB virus
Starry sky’ appearance
soilid
Hodgkin's Disease
Autoimmune war
No tumor in node
Reed-Sternberg: Bi nucleate cell, popcorn
Bi modal distro
Nodular Sclerosis Pattern
Stage 1
SINGLE NODE/ site
Stage 2
2 or more on same side of Diaphragm
Stage 3
Both sides of diaphragm
Stage 4
Multiple disseminated foci
liver & BM
Multiple Myeloma
Plasma cell malignancy
many groups in BM
Bleeding - Protein coats platelets
High IgG, Kappa chains
Arteriolosclerosis
Sm vessels
Atherosclerosis
fatty plaques
large arteries
Hyperhomocystinemia

• Hollenhorst plaque
Atheromas
Intimal lesions
large arteries
fiberous cap - necrotic core
Arteriolosclerosis
Areteriols
DM
HTN
○ Saccular or berry
Aneurysm
round, small
congenital
Fusiform Aneurysm
Really big
Micro aneurysm
Retina
congenital - neural
DM, HTN
vasculitis
Recurent Uveitis / Scleritis -> autoimmune
Syphilis
PAN
Giant Cell (Temporal) Arteritis
Polyarteritis nodosa (PAN)
Vasculitis
sm - med arteries
Hep B, autoimmune
Skin ulcers
hurts Kidneys --> HTN
scleritis, uveitis
Giant Cell (Temporal) Arteritis
Granulomatous
most common Vasculitis

• Diagnosis by ↑ ESR, CRP and biopsy of TA
Wegener Granulomatosis
• Necrotizing vasculitis, granulomas
Runny nose, sinuses inflammed
Lungs, kidneys
Behçet Disease
Vasculitis of small vessels

• HLA-B51
• Genital ulcers
• Ocular inflammation (uveitis)
(Often arthritis, NS symptoms
Reynaud Phenomenon
Emotional, mensies
hyper sympathetic
vasoconstriction
migranes
• Primary Reynaud (also called Raynaud Disease)
Idiopathic

• Smoking, caffeine worsen
• Secondary Reynaud (Reynaud Syndrome)
Assoc with severe autoimmune / obstructive disorders, drugs,
Thrombophlebitis
Slow blood --> thrombus in vien
embolize --> lung --> dead
Vascular ectasia
Dilation of vessel, not true tumor
Nevus flammeus
Cork Wine stain
Glaucoma
associated w/Sterg Webber Syndrome (Tard)
Hemangiomas Cavernous
Can get worse
associated with Von Hipple Lindow disease (retinal neoplasims)
Retinal Hemangioma
Congenital
don't change
Kaposi Sarcoma
Vascular neoplasm, proliferation endo
Slit like channels
Mediterranean man
AIDS
Herpes
AngioSarcoma
Malignant form of Kaposi
proliferation of endo
• Often involve skin, breast, liver
Von Hippel-Lindau Disease
Autosomal dominant

• Hemangioblastomas in cerebellum, spinal cord, kidney, retina
• Mutation of VHL tumor suppressor