Combined treatment of steroids and cyclosporine in Kimura disease

被引:40
作者
Sato, Satoshi [1 ]
Kawashima, Hisashi [1 ]
Kuboshima, Shinji [1 ]
Watanabe, Kiyoko [1 ]
Kashiwagi, Yasuyo [1 ]
Takekuma, Kouji [1 ]
Hoshika, Akinori [1 ]
机构
[1] Tokyo Med Univ, Dept Pediat, Shinjuku Ku, Tokyo 1600023, Japan
关键词
Kimura disease; cyclosporine; interleukin; Th2; eosinophils;
D O I
10.1542/peds.2006-0487
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Kimura disease is a rare but distinctive chronic eosinophilic inflammatory disorder that is characterized by tumor-like lesions in the soft tissue and lymph nodes of the head and neck or parotid gland. Recently, many immunopathogenetic features of underlying T lymphocytes and related cytokines have been noted in Kimura disease. However, few previous studies have investigated the serial levels of cytokines in children. In this report we describe an 11-year-old Japanese boy with relapsing Kimura disease. Before the diagnosis of Kimura disease, the patient had a swelling on his left neck. Steroids were effective, but the tumor relapsed within a few months as the steroids were tapered. He was treated with steroids and cyclosporine. This treatment was done by measuring serial levels of serum soluble interleukin-2 receptor, interleukin-4, interleukin-5, and eosinophil cationic protein. These results suggest the activation of T-helper cells and T-helper 2 cytokines, that after activated B cells and eosinophilic infiltration play an important role in Kimura disease, and that cyclosporine suppresses the activity of this disease.
引用
收藏
页码:E921 / E923
页数:3
相关论文
共 13 条
[1]   Eotaxin-3 and a uniquely conserved gene-expression profile in eosinophilic esophagitis [J].
Blanchard, C ;
Wang, N ;
Stringer, KF ;
Mishra, A ;
Fulkerson, PC ;
Abonia, JP ;
Jameson, SC ;
Kirby, C ;
Konikoff, MR ;
Collins, MH ;
Cohen, MB ;
Akers, R ;
Hogan, SP ;
Assa'ad, AH ;
Putnam, PE ;
Aronow, BJ ;
Rothenberg, ME .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (02) :536-547
[2]   Steroid-resistant nephrotic syndrome associated with Kimura's disease [J].
Chartapisak, W ;
Opastirakul, S .
AMERICAN JOURNAL OF NEPHROLOGY, 2002, 22 (04) :381-384
[3]   Kimura's disease: an unusual cause of cervical tumour [J].
Chusid, MJ ;
Rock, AL ;
Sty, JR ;
Oechler, HW ;
Beste, DJ .
ARCHIVES OF DISEASE IN CHILDHOOD, 1997, 77 (02) :153-154
[4]   TREATMENT OF KIMURAS-DISEASE - A THERAPEUTIC ENIGMA [J].
DAY, TA ;
ABREO, F ;
HOAJSOE, DK ;
AARSTAD, RF ;
STUCKER, FJ .
OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 1995, 112 (02) :333-337
[5]   In vivo expression of IL-4, IL-5, IL-13 and IFN-γ mRNAs in peripheral blood mononuclear cells and effect of cyclosporin A in a patient with Kimura's disease [J].
Katagiri, K ;
Itami, S ;
Hatano, Y ;
Yamaguchi, T ;
Takayasu, S .
BRITISH JOURNAL OF DERMATOLOGY, 1997, 137 (06) :972-977
[6]  
KIMURA T, 1948, T SOC PATH JAP, V37, P179
[7]   Mast cells and T cells in Kimura's disease express increased levels of interleukin-4, interleukin-5, eotaxin and RANTES [J].
Kimura, Y ;
Pawankar, R ;
Aoki, M ;
Niimi, Y ;
Kawana, S .
CLINICAL AND EXPERIMENTAL ALLERGY, 2002, 32 (12) :1787-1793
[8]   Steroid-sensitive nephrotic syndrome associated with Kimura disease [J].
Nakahara, C ;
Wada, T ;
Kusakari, J ;
Kanemoto, K ;
Kinugasa, H ;
Sibasaki, M ;
Nagata, M ;
Matsui, A .
PEDIATRIC NEPHROLOGY, 2000, 14 (06) :482-485
[9]  
REED RJ, 1972, CANCER-AM CANCER SOC, V29, P489, DOI 10.1002/1097-0142(197202)29:2<489::AID-CNCR2820290239>3.0.CO
[10]  
2-X