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Pediatric intestinal Behçet disease complicated by myeloid malignancies.

Authors :
Kanamitsu K
Shimada A
Nishiuchi R
Shigemura T
Nakazawa Y
Koike K
Kodama Y
Shinkoda Y
Kawano Y
Yasui K
Sasaki K
Kajiwara R
Tsukahara H
Manabe A
Source :
International journal of hematology [Int J Hematol] 2017 Mar; Vol. 105 (3), pp. 377-382. Date of Electronic Publication: 2016 Nov 15.
Publication Year :
2017

Abstract

Behçet disease (BD) is rarely seen in children. Its clinical manifestations are believed to differ between pediatric and adult patients. The characteristics of BD complicated by myelodysplastic syndrome (MDS) are well established for adult patients; however, because only a few cases of pediatric-onset BD complicated by MDS have been reported, its clinical characteristics remain unknown. We here retrospectively review pediatric-onset BD complicated by myeloid malignancies in Japan, having identified five such patients. All patients were female and had gastrointestinal involvements, but lacked both major features of BD, i.e., uveitis and association with HLA-B51. All patients had advanced MDS or acute myeloid leukemia and received chemotherapy followed by hematopoietic stem cell transplantation. These five cases suggest that intestinal BD and myeloid malignancies have one or more pathophysiological mechanisms in common.

Details

Language :
English
ISSN :
1865-3774
Volume :
105
Issue :
3
Database :
MEDLINE
Journal :
International journal of hematology
Publication Type :
Academic Journal
Accession number :
27848185
Full Text :
https://doi.org/10.1007/s12185-016-2127-7