JaLCDOI 10.18926/AMO/40135
フルテキストURL 64_4_263.pdf
著者 Pavelić, Jasminka| Čulić, Srdjana| Čulić, Vida|
抄録 The occurrence of Langerhans cell histiocytosis (LCH) and another malignancy in the same patient is infrequent but has been recognized. The genetic changes that could be responsible for LCH and/or concomitant leukemia development are obscure. To the best of our knowledge, this is the first description of constitutional maternally derived inv (9) (p12;q13) in an LCH patient, and also of the development of common ALL Ph after LCH diagnosis and therapy. The potential significance of these findings [inv (9)LCHALL Ph] and their mutual relationship are unknown. Therefore, cooperative studies of large numbers of patients are needed to identify the common risk factors, if any.
キーワード acute lymphoblastic leukemia genetic changes langerhans cell histiocytosis
Amo Type Case Report
発行日 2010-08
出版物タイトル Acta Medica Okayama
出版者 Okayama University Medical School
開始ページ 263
終了ページ 265
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 English
著作権者 Okayama University Medical School
論文のバージョン publisher
査読 有り
PubMed ID 20802544
Web of Sience KeyUT 000281384400008