purpura
purpura
Classification of purpuras
A- Purpura associated with normal
numbers of platelets (non thrombocytopenic purpuras)
a- Henoch-Schonlein
purpura (anaphylactoid purpura).
b- Meningococcemia or
septicemia.
c- Toxic vasculitis: may
produce hemorrhagic rash as a reaction to drugs such as iodides.
d- Viral or rickettsial
infections.
e- Scurvy (vitamin C
deficiency).
2- Platelet function disorders
a-
Congenital platelet function defects (thrombasthenias).
b- Acquired platelet
function disorders: e.g. uremia.
c- Drug-induced
abnormalities of platelet aggregation (salicylates therapy).
B- Purpura associated with decreased number of platelet (thrombocytopenic purpuras)
B- Purpura associated with decreased number of platelet (thrombocytopenic purpuras)
1- Idiopathic thrombocytopenic purpura (ITP).
2- Aplastic anemia.
3- Bone marrow infiltration e.g. leukemia.
4- hypersplenism.
5- Other thrombocytopenic purpura.
a- Drug induced
thrombocytopenia e.g carbamazepine.
b- Congenital
thrombocytopenic syndromes (e.g. Wiskott
Aldrich syndrome).
c- Thrombocytopenia with cavernous hemangioma.
6- Neonatal thrombocytopenia.
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