but is otherwise well. Blood: Hgb=11.1, WBC=6.3, Plt=14. What is the single most likely dx?
a. Acute leukemia
b. Aplastic anemia
c. HIV infection
d. ITP
e. SLE
answer: D
Acute immune
thrombocytopenia
ITP is caused by IgG autoimmune antibody to platelet cell
membrane antigens leading to platelet destruction in the spleen and liver.
Presentation
• Most present between ages of 2 and 5yrs, but can occur
at any age.
• 60% have preceding viral infection, e.g. upper
respiratory tract infection
(URTI).
• Bruising, purpura, petechiae, mucosal bleeding, menorrhagia.
• Intracranial bleeds very rare (< 0.5%); often
associated with trauma.
• Physical examination otherwise usually normal, e.g. no splenomegaly.
Investigation
• FBC: platelet count low, commonly platelet
size increased due to compensatory megakaryocytosis. Otherwise FBC is usually
normal.
• Testing for platelet antibodies is not
clinically useful.
• Bone marrow in ITP normal,
but striking increase in megakaryocytes.
Generally, bone marrow aspirate not indicated if the
child is otherwise well, unless concurrent pancytopenia, hepatosplenomegaly,
lymphadenopathy, or abnormally-increased blasts on FBC suggesting alternative
diagnosis, e.g. aplastic anaemia, acute leukaemia, SLE (adolescent girls) or
bone marrow failure syndrome.
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