Mediterranean Journal of Hematology and Infectious Diseases (Dec 2011)

Pseudo-differentiation syndrome

  • Dina Khalaf,
  • Fathi Jehani

DOI
https://doi.org/10.4084/mjhid.2011.061
Journal volume & issue
Vol. 3, no. 1
pp. e2011061 – e2011061

Abstract

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A patient with relapsed acute myeloid leukemia (AML) (M2) FAB classification developed a differentiating syndrome upon receiving Decitabine therapy given with palliative intent. The patient presented with high grade fever, constitutional symptoms and severe chest symptoms with no underlying lung condition. Chest x-ray (CXR) showed diffuse pulmonary infiltrates. Septic work up followed by intravenous broad spectrum antimicrobials did not improve his condition. Pan cultures’ results were repeatedly negative. Treatment with high dose Dexamethasone (DXM) resulted in marked clinical and radiological improvement. Our patient initially presented with relapsed AML (M2) Fab classification with t (8; 21); negative FMS-like tyrosine kinase -internal tandem duplication (FLT3-ITD) which are all good prognostic factors, yet the patient had an atypical clinical course with early frequent relapses, differentiation syndrome associated with Decitabine therapy and late in his disease, he developed a granulocytic sarcoma.

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