Abstract
We report a rare case of a patient with acute myeloid leukemia following refractory anemia with excess of blasts transformed (RAEB-T) who presented a clinical picture suggestive of thrombophlebitis. The ultrasonographic procedure and the response to corticosteroid treatment suggest that this condition was compatible with an atypical Sweet's syndrome.
Lingua originale | English |
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pagine (da-a) | 261-263 |
Numero di pagine | 3 |
Rivista | Panminerva Medica |
Volume | 41 |
Stato di pubblicazione | Pubblicato - 1999 |
Keywords
- Anemia, refracting, with excess of blasts
- Sweet's syndrome
- Leukemia, myelocytic, acute