Urticaria and systemic disease;Urticaire et maladies systémiques

Annales de Dermatologie et de Venereologie

Volumn 128, Issue 10 II, 2001, Pages 1156-1160

  Machet, L ^a   Wattier, H ^a   Vaillant, L ^a  

^a UNIVERSITY HOSPITAL OF TOURS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIHISTAMINIC AGENT; ANTIMALARIAL AGENT; BISPHOSPHONIC ACID DERIVATIVE; CEFACLOR; CEPHALOSPORIN DERIVATIVE; CIMETIDINE; COLCHICINE; CORTICOSTEROID; CYCLINE; DAPSONE; DILTIAZEM; FLUOXETINE; HYDANTOIN; IMMUNOSUPPRESSIVE AGENT; LYMPHOCYTE ANTIBODY; METHOTREXATE; NONSTEROID ANTIINFLAMMATORY AGENT; POTASSIUM; SULFANILAMIDE; VACCINE;

ARTICLE; FAMILIAL DISEASE; HUMAN; JUVENILE RHEUMATOID ARTHRITIS; MASTOCYTOSIS; SCHNITZLER SYNDROME; SYSTEMIC DISEASE; THYROID DISEASE; URTICARIA; VASCULITIS;

ADOLESCENT; ADULT; ANGIONEUROTIC EDEMA; CHILD; CHRONIC DISEASE; HUMANS; INFANT, NEWBORN; LUPUS ERYTHEMATOSUS, SYSTEMIC; MASTOCYTOSIS; RISK FACTORS; SCHNITZLER SYNDROME; SJOGREN'S SYNDROME; URTICARIA; URTICARIA PIGMENTOSA; VASCULITIS;

EID: 0035160687     PISSN: 01519638     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (42)

1. Urticaires et angio-œdèmes
2. Urticarial vasculitis: A histopathological and clinical review of 72 cases
3. Urticarial vasculitis
4. Clinicopathologic correlation of hypocomplementemia and normocomplementemic urticarial vasculitis
5. Systemic lupus erythematosus presenting with normocomplementemic urticarial vasculitis in a 4-year-old girl
6. Hypocomplementemic urticarial vasculitis: Association with chronic obstructive pulmonary disease
7. Hypocomplementemic urticarial vasculitis or systemic lupus erythematosus?
8. Hypocomplementaemic urticarial vasculitis: Successful treatment with cyclophosphamide-dexamethasone pulse therapy
9. Hepatitis B surface antigen deposition in the blood vessel walls of urticarial lesions in acute hepatitis B
10. Testing for hepatitis B virus in patients with chronic urticaria and angioedema
11. Systemic vasculitis in patients with hepatitis C
12. Cutaneous vasculitis and rheumatoid factor positivity as presenting signs of hepatitis C virus-induced mixed cryoglobulinemia
13. Treatment of refractory, symptomatic, hepatitis C virus related mixed cryoglobulinemia with ribavirin and interferon-alpha
14. Unusual cutaneous manifestations of systemic lupus erythematosus: I. Urticaria-like lesions. Correlation with clinical and serological abnormalities
15. Cutaneous manifestations of systemic lupus erythematosus
16. Autoantibodies in systemic lupus erythematosus and urticarial vasculitis
17. Acquired inhibitor deficiency revealing systemic lupus erythematosus
18. Cutaneous manifestations of primary Sjögren's syndrome: A reflection of vasculitis and association with anti-Ro (SSa) antibodies
19. 1q deficiency caused by monoclonal paraproteinaemia
20. Physiopathologie des toxidermies
21. The Schnitzler syndrome: Four new cases and review of the literature
22. Schnitzler's syndrome (urticaria and macroglobulinemia): Evolution to Waldenstrom's disease is not uncommon
23. Urticarial pathology in Schnitzler's (hyper-IgM) syndrome
24. Anti-interleukin-1 alpha autoantibodies in humans: Characterization, isotype distribution, and receptor-binding inhibition-higher frequency in Schnitzler's syndrome (urticaria and macroglobulinemia)
25. Chronic urticaria, arthralgia, raised erythrocyte sedimentation rate and IgG paraproteinaemia: A variant of Schnitzler's syndrome?
26. Urticaire chronique et thyroïdites auto-immunes
27. Chronic urticaria and angioedema associated with thyroid autoimmunity: Review and therapeutic implications
28. Muckle-Wells syndrome: Case report and review of cutaneous pathology
29. Genetic linkage of the Muckle-Wells syndrome to chromosome 1q44
30. Hyper IgD et urticaire familiale chez l'enfant
31. Cutaneous manifestations and histologic findings in the hyperimmunoglobulinemia D syndrome
32. International Hyper-IgD Study Group: Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome
33. Comparative study of 6 types of criteria in adult Still's disease
34. Manifestations cutanées de la maladie de Still de l'adulte. A propos de 4 observations
35. Serum Ferritin and isoferritinins are tools for diagnosis of active adult Still's disease
36. A chronic, infantile, neurological, cutaneous and articular (CINCA) syndrome. A specific entity analysed in 30 patients
37. Infantile-onset arthritis and multisystem inflammatory disease: "A new syndrome"
38. Les mastocytoses
39. Clinical advance in mastocytosis: An interdisciplinary round table discussion
40. Diagnostic criteria and classification of mastocytosis: A consensus proposal
41. Cutaneous mastocytosis in adults: Evaluation of 14 patients with respect to systemic disease manifestation
42. Bone marrow mast cell morphologic features and hematopoietic dyspoiesis in systemic mast cell disease