Blood Disorders
Pyramedz

Blood Disorders

Advanced treatment of blood cancers like lymphoma and leukemia, bone marrow and stem cell transplant, and care for sickle cell anemia, thalassemia and hemophilia with a specialist team

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Why Choose Blood Disorder Treatment in Egypt?

Advanced Treatment of Blood Cancers

Assessment and treatment of lymphoma, leukemia and multiple myeloma with chemotherapy, targeted therapy and immunotherapy, and bone marrow transplant in suitable cases, coordinated with the oncology team.

An Experienced Bone Marrow Transplant Programme

Bone marrow and stem cell transplant for children and adults, with donor matching (HLA matching) and full care before and after the transplant.

Specialist Care for Inherited Blood Disorders

Experience with sickle cell anemia, thalassemia, hemophilia and G6PD deficiency, conditions with high prevalence across the Gulf and the Middle East.

Accurate Diagnosis and a Clear Plan

A full work-up for anemia, iron and vitamin B12 deficiency and low platelets, and a decision on whether the case needs medical follow-up or an advanced treatment plan.

Pyramedz blood disorder treatment

A consultation to review blood reports and set the treatment plan

The details and cost of blood disorder treatment vary by diagnosis and whether the case needs a transplant or medical follow-up. Send us the blood count and reports, and our team will coordinate a case review with a hematology consultant and outline the suggested steps with an approximate quote.

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Frequently Asked Questions

These include anemia, iron and vitamin B12 deficiency, sickle cell anemia (sickle cell disease), thalassemia (mediterranean anemia), hemophilia and bleeding disorders, low platelets (thrombocytopenia), G6PD deficiency, as well as leukemia, lymphoma and multiple myeloma.

After a review of the pathology report and bone marrow studies, the haematology team, working with the oncology team, sets a plan that may include chemotherapy, targeted therapy and immunotherapy, followed by a bone marrow transplant in suitable cases. No treatment is presented as a guaranteed cure, and the plan is set case by case. For solid tumours and cancer surgery, see the cancer treatment page.

A bone marrow (or stem cell) transplant replaces diseased marrow with healthy cells from a matched donor or from the patient. It is recommended in selected cases of leukemia, thalassemia, sickle cell anemia and marrow failure, and the hematology consultant decides whether it is suitable for each case.

HLA tissue-typing tests are done for the patient and family members first, and a brother or sister is often the best source of a matched bone marrow donor. If there is no family donor, a search is made through donor registries.

A bone marrow transplant from a matched donor is the only treatment that may permanently remove the need for blood transfusions in selected thalassemia cases, particularly in children. The decision depends on the patient's age, condition and donor availability, and is discussed in detail by the hematology consultant.

In selected cases, a stem cell transplant is used to treat sickle cell anemia. Eligibility is assessed individually based on disease severity, complications and the availability of a matched donor.

Cost varies by transplant type (autologous or from a donor), the patient's condition, and the length of the hospital stay. Contact us on WhatsApp for a report review and an approximate quote.

This covers assessing the type and severity of hemophilia, a treatment plan with clotting factors, bleeding-prevention guidance, and regular follow-up with the hematology consultant.

Bring the most recent complete blood count (CBC), iron and vitamin B12 results, any bone marrow or genetic test reports, and previous transfusion or treatment records. You can send these to us before travelling.