| Literature DB >> 35386486 |
Lizeth Yamile Urrea Pineda1, Oliver Perilla2, Vanessa Santiago-Pacheco3, Simon Trujillo Montoya4.
Abstract
The 8p11 myeloproliferative syndrome (EMS) is an aggressive neoplasm associated with chromosomal translocations involving the fibroblast growth factor receptor 1 tyrosine kinase gene on chromosome 8p11. We report the case of a 31-year-old man with no prior medical history who presents with two weeks of sore throat and cervical lymphadenopathy up to 5 cm. Initial peripheral blood examination showed leukocytosis with predominantly neutrophils and eosinophilia. A CT scan demonstrated mediastinal lymphadenopathies, liver enlargement and splenomegaly. An excisional biopsy of a cervical lymph node demonstrated findings consistent with a diagnosis of T-cell lymphoblastic lymphoma. Bone marrow aspirate and biopsy revealed hypercellular marrow with granulocytic predominance, left-shifted granulopoiesis, eosinophilia and the cytogenetic analysis showed the following karyotype: 46, XY, t(8;13). The final diagnosis was a myeloproliferative syndrome with eosinophilia related to t(8;13) and T-cell acute lymphoblastic lymphoma (8p11 myeloproliferative syndrome). We review the relevant literature about this unusual entity.Entities:
Keywords: eosinophilia; fibroblastic growth factor receptor-1 gene (fgfr1); lymphadenopathy; myeloid leukemia; precursor t-cell lymphoblastic leukemia-lymphoma
Year: 2022 PMID: 35386486 PMCID: PMC8969320 DOI: 10.7759/cureus.22734
Source DB: PubMed Journal: Cureus ISSN: 2168-8184