Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
33 Cards in this Set
- Front
- Back
What is a thrombocytopenia?
|
decreased platelet count
|
|
what is a thrombocythemia?
|
an increased platelet count
|
|
what is a thrombocytopathy?
|
abnormal platelet function - they're defective.
|
|
What are some symptoms of platelet abnormalities and bleeding tendencies?
|
-Petechiae
-Ecchymoses -Epistxis/GI bleeds/menorrhagia -Bleed after surgery, cerebral |
|
What are the 4 types of thrombocytopenia?
|
1. Decreased plt production
2. Altered plt distribution 3. Ineffective production 4. Increased destruction |
|
What is the most common reason for a thrombocytopenia?
|
Increased platelet destruction, usually due to an autoimmune disorder.
|
|
What causes decreased platelets?
|
Decreased megakaryocytes in the bone marrow.
|
|
What are 2 reasons for decr. megakaryos in the bmarrow?
|
-Marrow aplasia
-Marrow infiltration -when in doubt say drugs! |
|
What are 5 spcf reasons you can give for dcr. plt production?
|
1. Viral infections
2. MDS 3. PNH 4. May-Hegglin Anomaly 5. Drug/toxin induced. |
|
what makes platelet distribution altered?
|
Spleen sequestrating the platelets, which occurs in hypersplenism.
|
|
What 2 diseases is spleen sequestration seen?
|
-Liver disease
-Portal hypertension |
|
What are 3 causes of ineffective thrombopoeisis?
|
1. Defective formation
2. Abnormal release to circultn 3. Destruction intramedullary |
|
What anemia is intramedullary destruction of plts seen in?
|
Vit B12/folate deficiency.
|
|
What are the 2 major categories of increased destruction plts?
|
-Immune
-Nonimmune |
|
What are 4 types of immune thrombocytopenia?
|
1. Autoimmune
2. Alloimmune 3. Drug-related 4. Neonatal infection. |
|
For thrombocytopenia, what is: -Primary autoimmune
-2ndary autoimmune |
Primary = ITP = idiopathic thrombocytopenia purpura.
2ndary = caused by infections, lupus, etc. |
|
What are 2 types of ITP?
In what patients? |
-Acute - children
-Chronic - adults, mostly female |
|
What ususally causes ITP?
|
-Acute from viral illness
-Chronic from Ab-coated platelets that spleeen destroys |
|
What is the treatment for each ITP?
|
-Acute/kids is self-limiting
-Chronic, use Cortisol |
|
What are symptoms of each ITP?
|
-Acute: purpura, ecchymoess, petechiae, mucosal bleeds
-Chronic: insidious onset |
|
What are some causes of 2ndary ITP?
|
Infections, lupus, refractory anemia, cancer, drugs
|
|
What 4 causes of alloimmmune thrombocytopenias?
|
-Neonatal alloimmune thrombocytopenia - mom immunizes fetus.
-After transfusion -make Ab to drug -Heparin-induced (IgG) |
|
What are the 3 main categories of non-immune thrombocytopenia?
|
-Microangiopathic
-Infection-induced -Hypersplenism |
|
What are the 3 types of Microangiopathic?
|
DIC, TTP, HUS
|
|
What is TTP? In Who?
|
Thrombotic thrombocytopenia purpura - young women
|
|
What IS DIC?
|
Dissemin. Intravasc Coagulopathy
-Simultaneous activation of coagulation and fibrinolysis. |
|
What types of infections induce thrombocytopenia?
|
-Viral
-Rickettsial -Malarial Fungal, protozoan, bacterial. |
|
what is pseudothrombocytopenia?
|
-Artifact caused by EDTA causing platelet clumps from improper collection.
|
|
Enzyme defect and accumulated product in Gaucher's disease:
|
-Beta-glucocerebrosidase
-Glucocerebroside |
|
Enzyme defect and accumulated product in Neimann-Pick:
|
-Sphingomyelinase
-Sphingomyelin |
|
Enzyme defect and accumulated product in sea-blue histiocytosis:
|
-Unknown
-Ceroid |
|
Enzyme defect and accumulated product in Tay-Sach's
|
-Hexosanimidase A
-Gangliosidase GM2 |
|
Enzyme defect/accumlated product in Mucopolysaccharidosis:
|
Can't break it down
|