Eosinophilic myositis with eosinophilic cellulitislike skin lesions - Association with increased serum levels of eosinophil cationic protein and interleukin-5

被引:25
作者
Trueb, RM
Lubbe, J
Torricelli, R
Panizzon, RG
Wuthrich, B
Burg, G
机构
[1] Department of Dermatology, University Hospital of Zurich, Zurich
[2] Department of Dermatology, University Hospital of Zurich, 8091 Zurich
关键词
D O I
10.1001/archderm.133.2.203
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Peripheral and tissue eosinophilia are associated with a group of idiopathic inflammatory syndromes. The idiopathic hypereosinophilic syndrome represents a spectrum of disorders characterized by prolonged eosinophilia of an undetectable cause and significant organ dysfunction. The pathogenic role of the eosinophil in these conditions is attested to by evidence of eosinophil activation and degranulation at sites of tissue injury. Recently, an overlapping range of idiopathic eosinophilic muscle disease with an overall good prognosis has been described. Results: We describe a patient with a syndrome of idiopathic myositis with eosinophilia and eosinophilic cellulitislike cutaneous manifestations. Histopathological studies of the skin and muscle revealed eosinophilic infiltration. Elevated serum levels of eosinophilic cationic protein and interleukin-5 paralleling disease activity were detected. Conclusions: This patient demonstrates clinical and laboratory features of eosinophilic myositis with eosinophilic cellulitislike skin lesions. The elevated serum levels of interleukin-5 and eosinophilic cationic protein may be responsible for the eosinophilia and tissue injury, respectively. With the advances in our understanding of cytokine-dependent regulatory mechanisms governing the eosinophil reaction, more targeted ways of manipulating eosinophilia as well as the entry and activation of eosinophils within specific tissues can be expected.
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页码:203 / 206
页数:4
相关论文
共 28 条
[1]   WELLS SYNDROME IS A DISTINCTIVE DISEASE ENTITY AND NOT A HISTOLOGIC DIAGNOSIS [J].
ABERER, W ;
KONRAD, K ;
WOLFF, K .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1988, 18 (01) :105-114
[2]   EPISODIC EOSINOPHILIA-MYALGIA LIKE SYNDROME IN A PATIENT WITHOUT L-TRYPTOPHAN USE - ASSOCIATION WITH EOSINOPHIL ACTIVATION AND INCREASED SERUM LEVELS OF GRANULOCYTE-MACROPHAGE COLONY STIMULATING FACTOR [J].
BOCHNER, BS ;
FRIEDMAN, B ;
KRISHNASWAMI, G ;
SCHLEIMER, RP ;
LICHTENSTEIN, LM ;
KROEGEL, C .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1991, 88 (04) :629-636
[3]   HYPEREOSINOPHILIC SYNDROME - ANALYSIS OF 14 CASES WITH REVIEW OF LITERATURE [J].
CHUSID, MJ ;
DALE, DC ;
WEST, BC ;
WOLFF, SM .
MEDICINE, 1975, 54 (01) :1-27
[4]   CARDIAC LOCALIZATION OF EOSINOPHIL-GRANULE MAJOR BASIC-PROTEIN IN ACUTE NECROTIZING MYOCARDITIS [J].
DEMELLO, DE ;
LIAPIS, H ;
JUREIDINI, S ;
NOURI, S ;
KEPHART, GM ;
GLEICH, GJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 323 (22) :1542-1545
[5]  
DESREUMAUX P, 1993, BLOOD, V82, P1553
[6]   THE IDIOPATHIC HYPEREOSINOPHILIC SYNDROME - CLINICAL, PATHOPHYSIOLOGIC, AND THERAPEUTIC CONSIDERATIONS [J].
FAUCI, AS ;
HARLEY, JB ;
ROBERTS, WC ;
FERRANS, VJ ;
GRALNICK, HR ;
BJORNSON, BH .
ANNALS OF INTERNAL MEDICINE, 1982, 97 (01) :78-92
[7]  
FUJISAWA T, 1990, J IMMUNOL, V144, P642
[8]   EPISODIC ANGIOEDEMA ASSOCIATED WITH EOSINOPHILIA [J].
GLEICH, GJ ;
SCHROETER, AL ;
MARCOUX, JP ;
SACHS, MI ;
OCONNELL, EJ ;
KOHLER, PF .
NEW ENGLAND JOURNAL OF MEDICINE, 1984, 310 (25) :1621-1626
[9]  
GLEICH GJ, 1992, BLOOD, V79, P688
[10]   HYPEREOSINOPHILIC SYNDROMES - ASSOCIATION WITH VASCULITIS, FIBROSIS AND AUTOIMMUNITY [J].
HALL, FC ;
WALPORT, MJ .
CLINICAL AND EXPERIMENTAL ALLERGY, 1993, 23 (07) :542-547