| Literature DB >> 16720555 |
Masahiko Sumi1, Kosuke Nunoda, Tomonori Mizutani, Yuko Ishii, Akihiko Gotoh, Yukihiko Kimura, Yasuhiro Suga, Tatsuo Ohira, Kuniharu Miyajima, Hiromi Serizawa, Kiyoshi Mukai, Harubumi Kato, Kazuma Ohyashiki.
Abstract
We report the case of a patient with hypereosinophilia and invasive thymoma harboring probable clonal proliferation of CD4+, CD8+, and CD25+ T-lymphocytes. A 64-year-old woman had eosinophilia (14.1 x 10(9)/L) and an anterior mediastinal tumor with elevated levels of serum immunoglobulin E (609.8 mg/dL) and interleukin 5 (239 pg/mL). Bone marrow aspirate showed marked infiltration by morphologically normal eosinophils with a normal karyotype but no FIP1L1-PDGFRA fusion gene. Flow cytometric analysis revealed an increasing number of CD3+/CD25+ lymphocytes in the peripheral blood, and the resected thymoma had infiltrated lymphocytes with CD4/CD8/CD25 antigens. Moreover, the thymoma had T-cell receptor rearrangements with a cytogenetically clonal nature, ie, t(2;4)(p22;q26). Although the number of patients with thymoma showing hypereosinophilia is small, this case suggests that a subset of patients with thymoma may have clonal expansion of T-lymphocytes with abnormal phenotypes that affect clinical manifestations, including hypereosinophilia.Entities:
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Year: 2006 PMID: 16720555 DOI: 10.1532/IJH97.05146
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490