Eosinophilic vasculitis in connective tissue disease

被引:40
|
作者
Chen, KR
Daniel, WP
Pittelkow, MR
Conn, DL
George, T
Leiferman, KM
机构
[1] MAYO CLIN & MAYO FDN, DEPT DERMATOL, ROCHESTER, MN 55905 USA
[2] MAYO CLIN & MAYO FDN, DIV RHEUMATOL INTERNAL MED, ROCHESTER, MN 55905 USA
关键词
D O I
10.1016/S0190-9622(96)90318-7
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Neutrophilic and lymphocytic vascular inflammation is common in vasculitis associated with connective tissue disease (CTD). We recently identified eight patients with CTD and eosinophilic vasculitis. Objective: The purpose of this study was to characterize a variant form of vasculitis in CTD with eosinophilic infiltration. Methods: Of 98 CTD patients with cutaneous necrotizing vasculitis, eight were found with predominantly eosinophilic vascular infiltration. Nine CTD patients with cutaneous neutrophilic vasculitis were identified for comparison. Clinical and laboratory findings were reviewed and compared. Indirect immunofluorescence for eosinophil granule major basic protein (MB), neutrophil elastase, and mast cell tryptase was performed on lesional tissue, MBP levels and eosinophil survival enhancing activity were assayed in sera from three patients. Results: The patients with eosinophilic vasculitis had depressed serum complement levels and peripheral blood eosinophilia; MBP levels were elevated in serum and eosinophil survival was prolonged. Immunofluorescence of tissue showed marked angiocentric eosinophil MBP staining with peripheral neutrophil elastase staining; mast cell tryptase staining was notably absent. The patients with neutrophilic vasculitis were variably hypocomplementemic and did not have peripheral blood eosinophilia. Immunofluorescence showed marked angiocentric neutrophil elastase staining with scattered eosinophil MBP staining; mast cell tryptase staining showed normal mast cell numbers. Conclusion: Patients with eosinophilic vasculitis, CTD, and hypocomplementemia show vessel wall destruction in association with vessel wall deposition of cytotoxic eosinophil granule MBP, which suggests that eosinophils mediate vascular damage in this disease process. In addition, perivascular mast cells appear diminished, thereby suggesting that mast cell degranulation occurs.
引用
收藏
页码:173 / 182
页数:10
相关论文
共 50 条
  • [1] Vasculitis associated with connective tissue disease
    Breedveld, FC
    BAILLIERES CLINICAL RHEUMATOLOGY, 1997, 11 (02): : 315 - 334
  • [2] VASCULITIS AND CONNECTIVE TISSUE DISEASE MIMICS
    Isenberg, David
    RHEUMATOLOGY, 2016, 55 : 12 - 12
  • [3] Interstitial disease associated with connective tissue disease and vasculitis
    Hernandez Muniz, S.
    Olivera Serrano, M. J.
    Jimenez Heffernan, J. A.
    Valenzuela, C.
    Caballero Sanchez-Robles, P.
    RADIOLOGIA, 2022, 64 : 250 - 264
  • [4] Eosinophilic gastrojejunitis associated with connective tissue disease
    Buchman, AL
    Wolf, D
    Gramlich, T
    SOUTHERN MEDICAL JOURNAL, 1996, 89 (03) : 327 - 330
  • [5] VASCULITIS AND CONNECTIVE-TISSUE DISEASE SYNDROMES
    WAGNER, BM
    HUMAN PATHOLOGY, 1985, 16 (10) : 969 - 969
  • [6] Imaging of finger vessels in connective tissue disease and vasculitis
    Schmidt, W. A.
    ANNALS OF THE RHEUMATIC DISEASES, 2007, 66 : 10 - 11
  • [7] Antiendothelial cell antibodies in vasculitis and connective tissue disease
    Belizna, C.
    Duijvestijn, A.
    Hamidou, M.
    Tervaert, J. W. Cohen
    ANNALS OF THE RHEUMATIC DISEASES, 2006, 65 (12) : 1545 - 1550
  • [8] CHRONIC EOSINOPHILIC PNEUMONIA IN THE SETTING OF UNDIFFERENTIATED CONNECTIVE TISSUE DISEASE
    Googe, B.
    Weeks, A. Q.
    JOURNAL OF INVESTIGATIVE MEDICINE, 2015, 63 (02) : 338 - 339
  • [9] Eosinophilic gastrointestinal disorders associated with autoimmune connective tissue disease
    Lecouffe-Desprets, Marie
    Groh, Matthieu
    Bour, Bruno
    Le Jeunne, Claire
    Puechal, Xavier
    JOINT BONE SPINE, 2016, 83 (05) : 479 - 484
  • [10] Splenic vasculitis in juvenile onset mixed connective tissue disease
    Akin, E
    Tucker, LB
    Miller, LC
    Schaller, JG
    JOURNAL OF RHEUMATOLOGY, 1998, 25 (07) : 1444 - 1445