Abstract |
Patients with myelodysplastic syndrome/myeloproliferative neoplasm (MDS/MPN) are often asymptomatic and thus can remain undiagnosed until they become symptomatic due to progression to the accelerated phase (AP) or transformation to acute leukemia (leukemic transformation; LT). We herein report the case of a previously healthy 38-year-old man who had hyperleukocytosis with dysplastic myeloid precursor cells and severe disseminated intravascular coagulation. Hematopoietic recovery with features of atypical chronic myeloid leukemia (aCML) after induction chemotherapy was a diagnostic clue. Although rare, this case highlights the limitation of the diagnostic approach for aCML with AP or LT at the initial presentation.
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Authors | Mai Fujita, Kazuharu Kamachi, Masako Yokoo, Keisuke Kidoguchi, Kana Kusaba, Haruna Kizuka-Sano, Kyosuke Yamaguchi, Atsujiro Nishioka, Mariko Yoshimura, Yasushi Kubota, Toshihiko Ando, Kensuke Kojima, Shinya Kimura |
Journal | Internal medicine (Tokyo, Japan)
(Intern Med)
Vol. 59
Issue 12
Pg. 1549-1553
(Jun 15 2020)
ISSN: 1349-7235 [Electronic] Japan |
PMID | 32188810
(Publication Type: Case Reports, Journal Article)
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Chemical References |
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Topics |
- Adult
- Antineoplastic Agents
(therapeutic use)
- Disseminated Intravascular Coagulation
(complications)
- Humans
- Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative
(complications, drug therapy, pathology)
- Leukocytosis
(complications)
- Male
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