Acute Lymphoblastic Leukemia with Hypereosinophilia: Report of a Case with 5q Deletion and Review of the Literature

Author:

Wynn Tung T.1,Heerema Nyla A.2,Hammond Sue3,Ranalli Mark1,Kahwash Samir B.3

Affiliation:

1. Section of Hematology/Oncology, Columbus Children's Hospital, 700 Children's Drive, Columbus, OH 43205, USA, USA

2. Department of Pathology, Division of Cytogenetics, Ohio State University, 167 Hamilton Hall, 1645 Neil Avenue, Columbus, OH 43210, USA

3. Department of Laboratory Medicine, Columbus Children's Hospital, 700 Children's Drive, Columbus, OH 43205, USA

Abstract

Peripheral blood eosinophilia as a presentation of acute lymphoblastic leukemia (ALL) has only rarely been reported. The eosinophilia is thought to be a nonneoplastic reaction to the neoplastic lymphoblasts. We present the case of a 5-year-old girl who developed peripheral hypereosinophilia with no circulating blasts prior to her diagnosis of B-cell lineage ALL. Cytogenetic study showed a hyperdiploid blast population with 5q deletion. Persistent peripheral hypereosinophilia should always be fully investigated, the possibility of a malignancy including ALL needs to be excluded, even in the absence of peripheral cytopenias and circulating blasts.

Publisher

SAGE Publications

Subject

General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology and Child Health

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