Title: Bleeding disorders
1Bleeding disorders
- Doc. MUDr. L. Boudová, Ph.D.
2Bleeding disordersI. Vessels - increased
fragilityII. Platelets - deficiency or
dysfunctionIII.Coagulation disordersIV.Combinati
on I-III
- I. Vessels
- infections, drugs (hypersensitivity)
- poor vascular wall Ehlers-Danlos, scurvy
Cushing syndrome, old people - hereditary hemorrhagic teleangiectasia
- amyloid
3Thrombocytes
- 150-300 000/mm3 normal
- 100 000/mm3 thrombocytopenia
- 50 000/mm3 posttraumatic bleeding
- 20 000/mm3 spontaneous bleeding
4Thrombocytopenia
- decreased production
- increased destruction
- sequestration
- dilution
5Splenomegaly
- a sign of an underlying disease
- a problem per se
- bigger spleen bigger function
- destruction of blood cells
- Hypersplenism
- splenomegaly
- (pan) cytopenia
- correction of blood cytopenia by splenectomy
6Immune thrombocytopenic purpura
- Idiopathic TP but autoimmune!
- Antibodies against platelets
- Primary or secondary
7ITP
- Acute children
- Abrupt onset, both sexes, 2 weeks after virosis,
resolves within 6 mo, 20 chronic - Chronic adults (FM 31)
- Petechial hemorrhages and ecchymoses
- Easy bruising, skin, mucosa, nose, gums, soft
tis., melena, hematuria, menstruation - Clin. nonspecific reflective of
thrombocytopenia
8ITP - organs
- Spleen - normal size
- PB megathrombocytes
- BM /- more megs
- Therapy splenectomy
9Thrombotic microangiopathiesrelated clinical
syndromesthrombotic thrombocytopenic purpura
(TTP)hemolytic-uremic syndrome
(HUS)ENDOTHELIAL INJURY WIDESPREAD HYALINE
MICROTHROMBI
- OVERLAP - common features (TTP, HUS)
- thrombocytopenia
- microangiopathic hemolytic anemia
- fever
10Thrombotic microangiopathiesthrombotic
thrombocytopenic purpura (TTP)hemolytic-uremic
syndrome (HUS)
- Versus
- Disseminated intravascular coagulation
- Common hyaline thrombi
- !!Differences DIC primary importance
-
- activation of clotting system
11Thrombotic microangiopathiesrelated clinical
syndromesthrombotic thrombocytopenic purpura
(TTP)hemolytic-uremic syndrome
(HUS)ENDOTHELIAL INJURY WIDESPREAD HYALINE
MICROTHROMBI
- OVERLAP - common features (TTP, HUS)
- thrombocytopenia
- microangiopathic hemolytic anemia
- fever
12Thrombotic microangiopathies
- TTP
- neurological deficits (transient)
- renal failure
- adult women
- HUS
- mostly no neurol. sympt.
- acute renal failure DOMINANT!
- children E. coli O157H7, verotoxin
Common thrombocytopenia, microangiopathic
hemolytic anemia, fever
13Microangiopathic hemolytic anemia
hemolytic-uremic syndrome several fragmented red
cells
14Thrombotic microangiopathiesthrombotic
thrombocytopenic purpura (TTP)hemolytic-uremic
syndrome (HUS)
- Versus
- Disseminated intravascular coagulation
- Common hyaline thrombi
- !!Differences DIC primary importance
-
- activation of clotting system
15Disseminated intravascular coagulation (DIC)
- secondary complication
- of some serious condition
- consumption coagulopathy
- thrombohemorrhagic diathesis
- acute, subacute, chronic
16DIC thrombotic and hemorrhagic diathesis
activation of coagulation sequence
- Microthrombi hypoxia, infarctions
- Consumption ?depletion of platelets and clotting
factors -
- secondary activation of fibrinolysis
hemorrhages
17Mechanisms of DIC trigger1. Release of tissue
factor or thromboplastic substances2.
Widespread endothelial injury
18DIC
- 1. obstetrics 50 abruptio placentae, retained
dead fetus, septic abortion, amniotic fluid
embolism, toxemia - 2. neoplasms 30 adenocarcinomas, AML
- 3. infections gram-negative sepsis
- 4. trauma, burns, extensive surgery
- 5. Other snakebite, heat stroke, giant
hemangioma, aortic aneurysm etc.
19DIC
- Morphology microthrombi
- Kidneys hemorrhages
- Microinfarcts, bilat. renal necrosis
- lungs
- Brain - microinfarcts, hemorrhage
- Placenta
- Spleen , liver
- Endocrine organs pituitary, adrenals
20DIC - clinical
- microangiopathic hemolytic anemia, RDS dyspnea,
cyanosis - neurologic symptoms, oliguria, acute renal and
circulatory failure, - Convulsions, coma
- SHOCK
21Disseminated intravascular coagulation
hyaline thrombi
22Sy Waterhouse - Friedrichsen