Total: 7 |
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PMID (PMCID) | ||
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11226524 |
FEMALE | |
Talc induced transfusion independence in a patient with myelodysplasia. | ||
Hirawat S, Arunabh A, Schulman P. Leuk Res. 2001;25(3):263-5. |
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Myelodysplasia with refractory anemia is associated with transfusion dependence. | ||
10390890 |
MALE | |
[Marked hematologic improvement despite deterioration of marrow cell dysplasia in a refractory anemia patient treated with vitamin D3]. | ||
Wakimoto N, Kimura F, Sato K, Kuwada N, Matsumura T, Yamashita T, Nakamura Y, Yoshida M, Nakamura Y, Motoyoshi K. Rinsho Ketsueki. 1999;40(5):408-13. |
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He was given a diagnosis of refractory anemia on the basis of bone marrow aspiration findings, which disclosed trilineage myelodysplasia. | ||
9389371 |
FEMALE | Middle Aged |
Sequential development of myelodysplasia and acute myeloid leukemia but with no karyotypic evolution after autografting in a patient with Philadelphia positive acute lymphoblastic leukemia. | ||
Saso R, Zomas A, Hamblin M, Dunlop L, Swansbury GJ, Min T, Singhal S, Powles R, Treleaven J, Mehta J. Leuk Lymphoma. 1997;26(5-6):625-8. |
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Moderate pancytopenia developed after 4 months, and myelodysplasia (refractory anemia) was diagnosed which rapidly evolved into AML. | ||
8689605 |
MIXED_SAMPLE | Child |
Trisomy 15 in hematological malignancies: six cases and review of the literature. | ||
Smith SR, Rowe D. Cancer Genet Cytogenet. 1996;89(1):27-30. |
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Four patients had myelodysplasia (refractory anemia), one patient each had acute myeloid leukemia and acute lymphoblastic leukemia. | ||
8560614 |
FEMALE | |
Bernard-Soulier-like functional platelet defect in myelodysplastic syndrome and in acute myeloblastic leukemia associated with trilineage myelodysplasia. | ||
Hicsonmez G, Gumruk F, Cetin M, Ozbek N, Tuncer M, Gursel T. Turk J Pediatr. 1995;37(4):425-9. |
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Platelet function was studied in a child with myelodysplastic syndrome (MDS: refractory anemia with an excess of blasts) and a child with acute myeloblastic leukemia (AML-M6) associated with trilineage myelodysplasia (TMDS). | ||
2179635 |
MIXED_SAMPLE | Adult |
Clinical characteristics of hybrid leukemia: report of five cases. | ||
Akashi K, Harada M, Shibuya T, Morioka E, Okamura T, Asano Y, Taniguchi S, Teshima T, Kikuchi M, Niho Y. Leuk Res. 1990;14(2):145-53. |
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Three of the five patients had been suffering from so-called stem cell disorders such as aplastic anemia in patient 2, trilineage myelodysplasia in patient 4 and refractory anemia with excess of blasts in transformation in patient 5. | ||
2588956 |
MALE | |
Systemic lupus erythematosus in a patient with refractory anemia. | ||
Nakayama S, Nakamura F, Yabe H, Nagai K. Nihon Ketsueki Gakkai Zasshi. 1989;52(6):1072-7. |
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A 69-year-old man was diagnosed as having refractory anemia (RA), accompanied by pancytopenia of two years' duration, myelodysplasia in all three cell lines, abnormal karyotype of 46, XY, 20q--in bone marrow cells, and positive antinuclear and DNA antibody tests. |