Idiopathic hypereosinophilic syndrome: A case evolving in B-lymphoblastic lymphoma

Maria Cristina Rapanotti, Roberta Caruso, Sergio Bernardini, Valentina Coletti, Francesco Lo-Coco, Giulio De Rossi

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Idiopathic hypereosinophilic syndrome (HES) is a rare disease characterized by tissue involvement and organ dysfunction due to abnormal eosinophil proliferation. Evolution of HES into myeloid or T-cell malignancies has been frequently reported. Here, we describe a case of HES that preceded the occurrence of a high-grade B-lymphoblastic lymphoma in which clonal evolution has been demonstrated at the molecular level.

Original languageEnglish
Pages (from-to)975-979
Number of pages5
JournalLeukemia Research
Volume29
Issue number8
DOIs
Publication statusPublished - Aug 2005

Fingerprint

Hypereosinophilic Syndrome
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Clonal Evolution
Rare Diseases
Eosinophils
T-Lymphocytes
Neoplasms

Keywords

  • B-cell clonality
  • Eosinophilic leukemia
  • Idiopathic hypereosinophilic syndrome

ASJC Scopus subject areas

  • Cancer Research
  • Hematology
  • Oncology

Cite this

Idiopathic hypereosinophilic syndrome : A case evolving in B-lymphoblastic lymphoma. / Rapanotti, Maria Cristina; Caruso, Roberta; Bernardini, Sergio; Coletti, Valentina; Lo-Coco, Francesco; De Rossi, Giulio.

In: Leukemia Research, Vol. 29, No. 8, 08.2005, p. 975-979.

Research output: Contribution to journalArticle

Rapanotti, MC, Caruso, R, Bernardini, S, Coletti, V, Lo-Coco, F & De Rossi, G 2005, 'Idiopathic hypereosinophilic syndrome: A case evolving in B-lymphoblastic lymphoma', Leukemia Research, vol. 29, no. 8, pp. 975-979. https://doi.org/10.1016/j.leukres.2005.01.010
Rapanotti, Maria Cristina ; Caruso, Roberta ; Bernardini, Sergio ; Coletti, Valentina ; Lo-Coco, Francesco ; De Rossi, Giulio. / Idiopathic hypereosinophilic syndrome : A case evolving in B-lymphoblastic lymphoma. In: Leukemia Research. 2005 ; Vol. 29, No. 8. pp. 975-979.
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