کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2140320 | 1088230 | 2015 | 4 صفحه PDF | دانلود رایگان |

• Case of essential thrombocythemia transformed to acute promyelocytic leukemia.
• Leukemia cells contained both t(15;17) and JAK2 V617F mutation.
• Severe differentiation syndrome in response to ATRA, possibly related to JAK2 V617F.
• JAK1/2 inhibitors may have clinical utility in differentiation syndrome.
Myeloproliferative neoplasms transformed into AML usually have a poor prognosis. We report a case of essential thrombocythemia with myelofibrosis that transformed into acute promyelocytic leukemia (APL) with both the t(15;17) translocation as well as the JAK2 V617F mutation. Clinically, this case was notable for severe differentiation syndrome despite treatment with high-dose dexamethasone. Cytokine production by differentiating APL cells was not directly abrogated by JAK2 inhibitors in vitro, suggesting that JAK2 V617F enhances the hyperinflammatory response downstream of cytokines. JAK1/2 inhibitors may therefore dampen the inflammatory cascade downstream of cytokine production, similar to glucocorticoids, and have a role in treating severe differentiation syndrome.
Journal: Leukemia Research Reports - Volume 4, Issue 1, 2015, Pages 8–11