Abstract |
A 67-year-old woman was treated with MP-P therapy and combination chemotherapy for multiple myeloma IgG-lambda type. After the therapy for about three years, pancytopenia developed. Bone marrow aspiration study revealed a few of myeloma cell and many atypical cells showing promyelocytic feature. Chromosomal abnormality was 46, X, -X, +8, -13, +mar. CD33 and CD56 were positive, but CD16 and HLA-DR were negative. We diagnosed as multiple myeloma complicated with secondary myeloid/natural killer (NK) cell acute leukemia. After she had been treated with low dose etoposide for leukemia, she obtained complete remission. But since myeloma progressed and the amount of M protein was increased, she was treated with dexamethasone and low dose etoposide, resulting in a decrease in the amount of M protein. After that, because of leukemic cell re-proliferation, she was treated with etoposide. However, she died of sepsis due to severe myelosuppression. This case was interesting one in coexist of multiple myeloma and secondary myeloid/NK cell acute leukemia, and those affecting her clinical course each other.
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Authors | H Kaya, S Nakamura, H Yamazaki, I Kumabashiri, S Ohtake, T Matsuda |
Journal | [Rinsho ketsueki] The Japanese journal of clinical hematology
(Rinsho Ketsueki)
Vol. 36
Issue 7
Pg. 682-6
(Jul 1995)
ISSN: 0485-1439 [Print] Japan |
PMID | 7563597
(Publication Type: Case Reports, English Abstract, Journal Article)
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Chemical References |
- Etoposide
- Dexamethasone
- Prednisolone
- Melphalan
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Topics |
- Aged
- Antineoplastic Combined Chemotherapy Protocols
(adverse effects)
- Dexamethasone
(administration & dosage)
- Etoposide
(administration & dosage)
- Fatal Outcome
- Female
- Humans
- Killer Cells, Natural
- Leukemia, Myeloid, Acute
(drug therapy, etiology)
- Melphalan
(administration & dosage, adverse effects)
- Multiple Myeloma
(drug therapy)
- Neoplasms, Second Primary
(drug therapy, etiology)
- Prednisolone
(administration & dosage, adverse effects)
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