Abstract
Acute promyelocytic leukaemia (APL) comprises approximately 10% of the acute myeloblastic leukaemias in adults [1,2]. The disease was first recognised as a distinctive clinical entity in the 1950s [3] and it typically presents with a severe bleeding diathesis that is exacerbated by chemotherapy [4–7]. This feature has led to a relatively high rate of early mortality, ranging from 8% to 47% in recent series [4–9], primarily as a consequence of intracranial haemorrhage [9–11]. In this chapter, we review the latest information regarding the molecular genetics and current methods of therapy of this disease.
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de Thé, H., Degos, L., Warrell, R.P. (1995). Clinical and Molecular Advances in Acute Promyelocytic Leukaemia. In: Degos, L., Parkinson, D.R. (eds) Retinoids in Oncology. ESO Monographs. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-79706-4_7
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