Langerhans cell histiocytosis following childhood acute lymphoblastic leukemia

Citation
A. Raj et al., Langerhans cell histiocytosis following childhood acute lymphoblastic leukemia, AM J HEMAT, 68(4), 2001, pp. 284-286
Citations number
13
Categorie Soggetti
Hematology,"Cardiovascular & Hematology Research
Journal title
AMERICAN JOURNAL OF HEMATOLOGY
ISSN journal
03618609 → ACNP
Volume
68
Issue
4
Year of publication
2001
Pages
284 - 286
Database
ISI
SICI code
0361-8609(200112)68:4<284:LCHFCA>2.0.ZU;2-Y
Abstract
Langerhans cell histiocytosis (LCH) is a clonal proliferation of Langerhans cells of unknown etiology that results in a range of clinical manifestatio ns. LICH has been known to be associated with a variety of malignant diseas es. A 7-year-old boy was treated for standard-risk acute lymphoblastic leuk emia (ALL) at age 2 years, on a Children's Cancer Group chemotherapy protoc ol for 3 years and developed LCH 2 years after completion of chemotherapy. The case and a review of literature on the association of LCH and ALL are p resented. (C) 2001 Wiley-Liss, Inc.