Equitani F, Mele L, Rutella S, Belli P, Paciaroni K, Piscitelli R, Pagano L
Hematology Chair, Catholic University, Rome, Italy.
Panminerva Med. 1999 Sep;41(3):261-3.
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.
我们报告了一例罕见病例,一名患者在难治性贫血伴原始细胞增多转化型(RAEB-T)后发生急性髓系白血病,其临床表现提示为血栓性静脉炎。超声检查及对皮质类固醇治疗的反应表明,这种情况符合非典型Sweet综合征。