Article citationsMore>>
Tsukasaki, K., Utsunomiya, A., Fukuda, H., Shibata, T., Fukushima, T., Takatsuka, Y., Ikeda, S., Masuda, M., Nagoshi, H., Ueda, R., Tamura, K., Sano, M., Momita, S., Yamaguchi, K., Kawano, F., Hanada, S., Tobinai, K., Shimoyama, M., Hotta, T. and Tomonaga, M., Japan Clinical Oncology Group Study J (2007) VCAP-AMPVECP Compared with Biweekly CHOP for Adult T-cell Leukemia-Lymphoma: Japan Clinical Oncology Group Study JCOG9801. Journal of Clinical Oncology, 25, 5458-5464. https://doi.org/10.1200/JCO.2007.11.9958
has been cited by the following article:
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TITLE:
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
AUTHORS:
Daouda Kone, Nicaise Yao Atimere, Line Couitchere, Gyna Loko
KEYWORDS:
ATLL, Sickle Cell Disease, HTLV1, Martinique
JOURNAL NAME:
Open Journal of Blood Diseases,
Vol.7 No.4,
December
28,
2017
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.
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