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A distinct form of Acute myeloid leukemia (AML) in which this chromosomal anomaly is found de novo or in therapy-related AML cases, and is characterized by frequent extramedullary involvement (mainly hepatomegaly, splenomegaly, lymphadenopathies, cutaneous infiltration, but also gum, bone, central nervous system, testicles involvement), severe coagulation disorder (disseminated intravascular coagulopathy or primary fibrinolysis) and poor prognosis. Morphologically, a blast population with a myelomonocytic stage of differentiation is observed.
Estimated prevalence: Unknown (Unknown prevalence).
No clinical trials have been registered for acute myeloid leukemia with t(8;16)(p11;p13) translocation.
3 publications have been identified in PubMed for acute myeloid leukemia with t(8;16)(p11;p13) translocation. Research spans Review / Meta-Analysis (33%), Case Report / Case Series (33%), and Clinical Trial Publication (33%).
Catana AC (2026). [PMID: 41753246](https://pubmed.ncbi.nlm.nih.gov/41753246/). *J Clin Med*. [Case Report / Case Series]
Schmälter AK (2025). [PMID: 39558209](https://pubmed.ncbi.nlm.nih.gov/39558209/). *Am J Hematol*. [Clinical Trial Publication]
Dai JW (2024). [PMID: 40032343](https://pubmed.ncbi.nlm.nih.gov/40032343/). *Zhonghua Xue Ye Xue Za Zhi*. [Review / Meta-Analysis]
Data assembled from 3 of 12 sources · Last updated Sep 21, 2026, 4:51 AM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about acute myeloid leukemia with t(8;16)(p11;p13) translocation