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DR Medhat MRCP

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• TTT :<br />

Elderly patients (the majority) : Conservative (e.g EPO & G-CSF)<br />

< 60 years old with AML transformation : Intensive chemotherapy +<br />

BM transplantation.<br />

• Prognosis of MDS :<br />

Very poor<br />

Median survival is two years.<br />

Patients are more likely to have serious infections or life-threatening bleeds than<br />

blastic transformation<br />

Pure red cell aplasia (PRCA):<br />

- It`s selective absence of erythroid progenators in an otherwise normal bone marrow.<br />

- It is diagnosed when there is unexplained anaemia and reticulocytopenia, with a<br />

complete absence of red cell precursors in the bone marrow, but with preservation<br />

of other cell lines.<br />

• Assciation:<br />

- Either spontaneously (Diamond-Blakfan syndrome) or associated with :<br />

Thymoma.<br />

Autoimmune.<br />

Lymphoproliferative disorders.<br />

Erythropoitin alpha TTT ( Abs against EPO react against red BM.)<br />

• Treatment : is supportive with immunosuppression e.g with cyclosporin<br />

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