Combination of Haemoglobinopathy and Haemopathy —(Adult T-Cell Lymphoma/Leukemia and Sickle Cell Disease: A Rare Case of Disease Observed in the Adult Referral Center of Sickle Cell Disease (CRD-A) in Martinique ()
ABSTRACT
Authors report a case of beta thalassemia combined with hematological malignant
(ATLL) in a 40-year-old female, cashier screened HTLV-1 positive;
followed since her 10 years old for the account of thalasso-sickle cell disease at
the adult referal center of sickle cell disease in Martinique. Therapeutic management
consisted of systemic chemotherapy, intrathecally-administered preventive
chemotherapy combined with a treatment based on bisphosphonate
and corticosteroid.
Share and Cite:
Kone, D. , Atimere, N. , Couitchere, L. and Loko, G. (2017) Combination of Haemoglobinopathy and Haemopathy —(Adult T-Cell Lymphoma/Leukemia and Sickle Cell Disease: A Rare Case of Disease Observed in the Adult Referral Center of Sickle Cell Disease (CRD-A) in Martinique.
Open Journal of Blood Diseases,
7, 103-107. doi:
10.4236/ojbd.2017.74010.
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