Hypereosinophilic syndrome and other rheumatic diseases with hypereosinophilia

被引：0
|
作者：
Schirmer, J. H. [1 ]
Hoyer, B. F. [1 ]
机构：
[1] Univ Klinikum Schleswig Holstein, Exzellenzzentrum Entzundungsmed, Sekt Rheumatol, Klin Innere Med 1, Campus Kiel,Arnold Heller Str 3, D-24105 Kiel, Germany
来源：
ZEITSCHRIFT FUR RHEUMATOLOGIE | 2019年 / 78卷 / 04期
关键词：
IgG4-related disease; Eosinophilic fasciitis; Drug-induced vasculitis; Eosinophilia-myalgia syndrome; Toxic oil syndrome; EOSINOPHILIA-MYALGIA-SYNDROME; POLYANGIITIS CHURG-STRAUSS; IGG4-RELATED DISEASE; GRANULOMATOSIS; RECOMMENDATIONS; CLASSIFICATION; NOMENCLATURE; FASCIITIS; INGESTION; STATEMENT;
D O I：
10.1007/s00393-019-0623-x
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
Among the eosinophilic diseases treated by rheumatologists other than eosinophilic granulomatosis with polyangiitis, there are further organ-related and systemic diseases with hypereosinophilia. Only the exact differential diagnostic demarcation of the diseases enables a pathogenetic oriented treatment. This article focuses on the hypereosinophilic syndromes. The potential differential diagnoses of Ig(immunoglobulin)G4-related disease, eosinophilic fasciitis and drug-induced vasculitis as well as eosinophilia-myalgia syndrome and toxic oil syndrome as historic drug-induced inflammatory rheumatic diseases are described and the clinical manifestations and treatment are summarized.
引用
收藏
页码：322 / 332
页数：11
相关论文
共 50 条
  • [1] Hypereosinophiles Syndrom und weitere rheumatische Erkrankungen mit HypereosinophilieHypereosinophilic syndrome and other rheumatic diseases with hypereosinophilia
    J. H. Schirmer
    B. F. Hoyer
    Zeitschrift für Rheumatologie, 2019, 78 (4) : 322 - 332
  • [2] TRANSIENT HYPEREOSINOPHILIA IN THE INFANT OF A MOTHER WITH HYPEREOSINOPHILIC SYNDROME
    CAREY, JP
    BURKE, AC
    CARTER, WH
    ARCHIVES OF INTERNAL MEDICINE, 1982, 142 (09) : 1754 - 1755
  • [3] HYPEREOSINOPHILIC DERMATITIS (NIR-WESTFRIED) A VARIANT OF HYPEREOSINOPHILIA SYNDROME
    OPPOLZER, G
    DUSCHET, P
    SCHWARZ, T
    HUTTERER, J
    GSCHNAIT, F
    ZEITSCHRIFT FUR HAUTKRANKHEITEN H&G, 1988, 63 (02): : 123 - 125
  • [4] A CASE OF MISTAKEN IDENTITY: HYPEREOSINOPHILIC SYNDROME VS SECONDARY HYPEREOSINOPHILIA
    Riverall, O.
    Ussui, V.
    Galant-Swafford, J.
    ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 2024, 133 (06) : S134 - S134
  • [5] Cutaneous hypereosinophilia ... Hypereosinophilic syndromes
    Aubert, H.
    Hamidou, M.
    Barbarot, S.
    Piriou, N.
    Lefebvre, M.
    Neel, A.
    ANNALES DE DERMATOLOGIE ET DE VENEREOLOGIE, 2020, 147 (02): : 154 - 154
  • [6] Hypereosinophilic Syndrome and Proliferative Diseases
    Ionescu, Marius A.
    Wang, Li
    Janin, Anne
    ACTA DERMATOVENEROLOGICA CROATICA, 2009, 17 (04) : 323 - 330
  • [7] BENIGN IDIOPATHIC HYPEREOSINOPHILIA - A FEEBLE MASQUERADER OR A SMOLDERING FORM OF THE HYPEREOSINOPHILIC SYNDROME
    CONFALONIERI, M
    TACCONI, F
    DEAMICI, M
    CAMILLO, RM
    PORTA, C
    GIOGLIO, L
    BOBBIOPALLAVICINI, E
    HAEMATOLOGICA, 1995, 80 (01) : 50 - 53
  • [8] MARKED HYPEREOSINOPHILIA IN A PATIENT WITH ASTHMA AND NASAL POLYPS CONFOUNDING HYPEREOSINOPHILIC SYNDROME
    Gupta, Samiksha
    Jain, Neha
    Raju, Shine
    CHEST, 2023, 164 (04) : 89A - 90A
  • [9] Episcleris, arthrofasciitis and hypereosinophilia: primary hypereosinophilic syndrome or atypical Wegener’s granulomatosis?
    Aline Defaveri do Prado
    Carlos Eduardo Poli de Figueiredo
    Carlo Domenico Marrone
    Vinícius Duval da Silva
    Domingos O. d’Avila
    Henrique Luiz Staub
    Rheumatology International, 2007, 28 : 89 - 90
  • [10] Episcleris, arthrofasciitis and hypereosinophilia: primary hypereosinophilic syndrome or atypical Wegener's granulomatosis?
    do Prado, Aline Defaveri
    de Figueiredo, Carlos Eduardo Poli
    Marrone, Carlo Domenico
    da Silva, Vinicius Duval
    d'Avila, Domingos O.
    Staub, Henrique Luiz
    RHEUMATOLOGY INTERNATIONAL, 2007, 28 (01) : 89 - 90
12345