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Retinoic acid syndrome (RAS) in an aplasic patient with secondary acute promyelocytic leukemia (APL)

✍ Scribed by L. Castagna; T. Bendahamane; J. H. Bourhis; J. N. Munck; A. Venuat; A. Ibrahim; J. Pico; M. Hayat

Book ID
114792175
Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
210 KB
Volume
57
Category
Article
ISSN
0902-4441

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## Abstract A 56‐year‐old woman with an acute promyelocytic leukemia (APL) developed a severe __all‐trans__‐retinoic (ATRA) syndrome on day 17 of treatment. Shortly after, she presented a picture of pancytopenia, hepatosplenomegaly, increased triglycerides, ferritin, and liver enzymes. A bone marro