Urticaria as a cutaneous sign of adult-onset Still's disease

被引:14
作者
Criado, Roberta F. J.
Criado, Paulo Ricardo
Vasconcellos, Cidia
Szajubok, Jose Carlos M.
Michalany, Nilceo S.
Kadunc, Bogdana Victoria
Costa Martins, Jose Eduardo
机构
[1] Fac Med ABC, Dept Dermatol, Allergy Unit, Santo Andre, Brazil
[2] Univ Sao Paulo, Fac Med, LIM 53 Hosp Clin, Sao Paulo, SP, Brazil
[3] Fac Med ABC, Dept Rheumatol, Dept Pathol, Santo Andre, Brazil
[4] Univ Fed Sao Paulo, Dept Pathol, Sao Paulo, Brazil
[5] Hosp Servidor Publ Municipal, Dermatol Unit, Sao Paulo, Brazil
关键词
D O I
10.2310/7750.2006.00017
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background. The cardinal signs and symptoms of adult-onset Still's disease (AOSD) include periodic fever, arthralgia and arthritis, lymphadenopathy, hepatosplenomegaly, an evanescent rash accompanied by neutrophilic granulocytosis, and a negative rheumatoid factor and antinuclear antibody test. Objective To alert clinicians and dermatologists to internal diseases such as AOSD when assisting patients with urticarial eruptions and systemic symptoms. Methods: A case report of a 52-year-old white woman who received conventional therapy for urticaria for 3 years, with no improvement. Following this period, a diagnosis of AOSD was performed based on the presence of systemic symptoms. Results: The inflammatory activity markers decreased by the second month of methotrexate therapy; however, the cutaneous lesions failed to disappear. Thalidomide was initiated, and total improvement of the cutaneous lesions was observed after 2 weeks. Conclusion: Urticarial rash is an uncommon presentation of AOSD, and clinicians must be alert to the possibility of a mis-diagnosis in these cases.
引用
收藏
页码:99 / 103
页数:5
相关论文
共 30 条
  • [1] Adult-onset Still's disease with atypical cutaneous features
    Affleck, AG
    Littlewood, SM
    [J]. JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2005, 19 (03) : 360 - 363
  • [2] Schnitzler's Syndrome with IgG κ Gammopathy
    Akimoto, R
    Yoshida, M
    Matsuda, R
    Miyasaka, K
    Itoh, M
    [J]. JOURNAL OF DERMATOLOGY, 2002, 29 (11) : 735 - 738
  • [3] Alonso R, 2002, J INVEST ALLERG CLIN, V12, P60
  • [4] STILL,S DISEASE IN ADULT
    BYWATERS, EG
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 1971, 30 (02) : 121 - +
  • [5] CALABRO JJ, 1986, J RHEUMATOL, V13, P827
  • [6] Cavagna L, 2001, CLIN EXP RHEUMATOL, V19, P329
  • [7] Medical progress: Hereditary periodic fever.
    Drenth, JPH
    van der Meer, JWM
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (24) : 1748 - 1757
  • [8] Proposal for a new set of classification criteria for adult-onset Still disease
    Fautrel, B
    Zing, E
    Golmard, JL
    Le Moel, G
    Bissery, A
    Rioux, C
    Rozenberg, S
    Piette, JC
    Bourgeois, P
    [J]. MEDICINE, 2002, 81 (03) : 194 - 200
  • [9] Persistent generalized erythema in adult-onset Still's disease
    Fujii, K
    Konishi, K
    Kanno, Y
    Ohgou, N
    [J]. INTERNATIONAL JOURNAL OF DERMATOLOGY, 2003, 42 (10) : 824 - 825
  • [10] Gambichler T, 2003, EUR J MED RES, V8, P527