| Literature DB >> 28259746 |
Maximilian Jameson-Lee1, Katherine Chen1, Ellen Ritchie1, Tsiporah Shore1, Omar Al-Khattab2, Usama Gergis3.
Abstract
Thrombocytopenia with absent radii (TAR) syndrome is a rare congenital disorder characterized by low platelet counts of various severity, bilateral absent radii but thumbs are usually present. TAR syndrome is not generally associated with bone marrow failure or malignancy. Janus kinase-2, myeloproliferative leukemia protein, and calreticulin are not mutated in TAR patients. Only four cases of leukemia were reported in TAR patients in the literature: three acute myeloid leukemia (AML) and one acute lymphoblastic leukemia. Of the three cases of AML found in TAR patient, only one was reported in an adult. We report a case of myelodysplastic syndrome progressing to AML with calreticulin driver mutation in an adult male with TAR syndrome who was successfully treated with hematopoietic allogeneic stem cell transplantation.Entities:
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Year: 2017 PMID: 28259746 DOI: 10.1016/j.hemonc.2017.02.001
Source DB: PubMed Journal: Hematol Oncol Stem Cell Ther