Successful treatment of chronic recurrent multifocal osteomyelitis with tumor necrosis factor-α blockage

被引:87
作者
Deutschmann, A
Mache, CJ
Bodo, K
Zebedin, D
Ring, E
机构
[1] Med Univ Graz, Dept Pediat, A-8036 Graz, Austria
[2] Med Univ Graz, Dept Radiol, A-8036 Graz, Austria
[3] Med Univ Graz, Inst Pathol, A-8036 Graz, Austria
关键词
D O I
10.1542/peds.2004-2206
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
We describe the case of an 18-year-old girl with chronic recurrent multifocal osteomyelitis (CRMO) over a period of 10 years. She had suffered predominantly from very painful recurrent swelling of her cheeks. Various therapeutic regimens including nonsteroidal antiinflammatory drugs and steroids had shown only a partial or temporary response. Because tumor necrosis factor-alpha-blocking agents have been successfully applied in Crohn's-associated CRMO and the related SAPHO ( synovitis, acne, pustulosis, hyperostosis, and osteitis) syndrome, tumor necrosis factor-alpha-blocking therapy with infliximab was initiated. Thereafter, apart from 1 mild episode, no additional recurrences were observed during 21 months of follow-up. Infliximab was well tolerated, and steroids were tapered off. Our observation indicates that infliximab may be an effective therapeutic option in CRMO.
引用
收藏
页码:1231 / 1233
页数:3
相关论文
共 9 条
[1]  
Baghai M, 2001, MAYO CLIN PROC, V76, P653
[2]   The tumor necrosis factor ligand and receptor families [J].
Bazzoni, F ;
Beutler, B .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (26) :1717-1725
[3]   Crohn's-associated chronic recurrent multifocal osteomyelitis responsive to infliximab [J].
Carpenter, E ;
Jackson, MA ;
Friesen, CA ;
Scarbrough, M ;
Roberts, CC .
JOURNAL OF PEDIATRICS, 2004, 144 (04) :541-544
[4]   Chronic recurrent multifocal osteomyelitis in children:: Diagnostic value of histopathology and microbial testing [J].
Girschick, HJ ;
Huppertz, HI ;
Harmsen, D ;
Krauspe, R ;
Müller-Hermelink, K ;
Papadopoulos, T .
HUMAN PATHOLOGY, 1999, 30 (01) :59-65
[5]   Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22 [J].
Golla, A ;
Jansson, A ;
Ramser, J ;
Hellebrand, H ;
Zahn, R ;
Meitinger, T ;
Belohradsky, BH ;
Meindl, A .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2002, 10 (03) :217-221
[6]   Successful treatment of SAPHO syndrome with infliximab: report of two cases [J].
Olivieri, I ;
Padula, A ;
Ciancio, G ;
Salvarani, C ;
Niccoli, L ;
Cantini, F .
ANNALS OF THE RHEUMATIC DISEASES, 2002, 61 (04) :375-376
[7]   Chronic recurrent multifocal osteomyelitis [J].
Schilling, F ;
Kessler, S .
KLINISCHE PADIATRIE, 2001, 213 (05) :271-276
[8]   SAPHO: Rare or just not recognized? [J].
Van Doornum, S ;
Barraclough, D ;
McColl, G ;
Wicks, I .
SEMINARS IN ARTHRITIS AND RHEUMATISM, 2000, 30 (01) :70-77
[9]   Sustained response to tumor necrosis factor α-blocking agents in two patients with SAPHO syndrome [J].
Wagner, AD ;
Andresen, J ;
Jendro, MC ;
Hülsemann, JL ;
Zeidler, H .
ARTHRITIS AND RHEUMATISM, 2002, 46 (07) :1965-1968