A case of MDS/MPN overlap syndrome with ring sideroblasts and thrombocytosis: Tackling the quandary of thrombosis versus hemorrhage

Author:

Cherniawsky Hannah1,Razavi Habib Moshref23ORCID

Affiliation:

1. Division of Haematology, Department of Medicine University of British Columbia Vancouver British Columbia Canada

2. Division of Hematopathology and Transfusion Medicine, Fraser Health Authority University of British Columbia Vancouver British Columbia Canada

3. Department of Pathology and Laboratory Medicine University of British Columbia Vancouver British Columbia Canada

Abstract

Key Clinical MessageNo formal treatment guidelines for MDS/MPN‐RS‐T exist. With salient features such as anemia and thrombocytosis, management is individualized and aims to address anemia, thrombosis, and in some cases acquired von Willebrand's disease.AbstractMyelodysplastic/myeloproliferative overlap syndrome with ring sideroblasts and thrombocytosis (MDS/MPN‐RS‐T) is a rare myeloid neoplasm showing myelodysplastic and myeloproliferative features. With extremely raised platelets, possibility of acquired von Willebrand and risk of hemorrhage is increased. With this quandary in mind, a descriptive case and a brief discussion of available treatments ensues.

Publisher

Wiley

Subject

General Medicine

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