A successful challenge in a patient with vancomycin-induced linear IgA dermatosis

被引:15
作者
Joshi, S [1 ]
Scott, G [1 ]
Looney, RJ [1 ]
机构
[1] Univ Rochester, Med Ctr, Dept Allergy Immunol Rheumatol, Rochester, NY 14642 USA
关键词
D O I
10.1016/S1081-1206(10)61454-8
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Linear IgA bullous dermatosis (LABD), a subepidermal, blistering skin disease, is generally believed to be idiopathic. It has been reported in association with multiple medications, including vancomycin. In each case, complete clearance of the skin lesions occurred with discontinued use of the drug. A subsequent rechallenge reproduced the eruption within hours to days. Objective: To present a patient with vancomycin-associated LABD who underwent a successful challenge with the antibiotic 4 years after the initial reaction. Methods: The patient developed blistering lesions over her trunk and extremities 10 days after the initiation of vancomycin for sepsis. A biopsy specimen of a skin eruption was consistent with linear IgA dermatosis. Following discontinued use of the drug, her skin lesions resolved. Four years later, she required vancomycin for osteomyelitis. Results: The patient underwent a vancomycin-graded challenge of 5 doses over 5 days. On day 1, she received 10 mg, and this was increased in a semilog fashion to 1,000 mg on day 5. She had no recurrence of her skin lesions. Conclusions: This is the first case, to our knowledge, to show a successful rechallenge in a patient with drug-associated LABD. Since the patient did not have a reaction to the challenge, it is possible that the IgA antibodies responsible for drug-induced LABD are only present transiently and diminish over time.
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页码:101 / 103
页数:3
相关论文
共 14 条
[1]  
ARGENYI ZB, 1987, CLEV CLIN J MED, V54, P445
[2]   VANCOMYCIN-INDUCED LINEAR IGA BULLOUS DERMATOSIS [J].
BADEN, LA ;
APOVIAN, C ;
IMBER, MJ ;
DOVER, JS .
ARCHIVES OF DERMATOLOGY, 1988, 124 (08) :1186-1188
[3]   VANCOMYCIN-ASSOCIATED LINEAR IGA DERMATOSIS - A REPORT OF 3 CASES [J].
CARPENTER, S ;
BERG, D ;
SIDHUMALIK, N ;
HALL, RP ;
RICO, MJ .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1992, 26 (01) :45-48
[4]  
GABRIELSEN TO, 1981, ACTA DERM-VENEREOL, V61, P439
[5]   BULLOUS PEMPHIGOID-LIKE LESIONS INDUCED BY PHENACETIN - REPORT OF A CASE AND AN IMMUNOPATHOLOGIC STUDY [J].
KASHIHARA, M ;
DANNO, K ;
MIYACHI, Y ;
HORIGUCHI, Y ;
IMAMURA, S .
ARCHIVES OF DERMATOLOGY, 1984, 120 (09) :1196-1199
[6]  
KLEIN LE, 1989, CUTIS, V44, P393
[7]   DRUG-INDUCED LINEAR IGA BULLOUS DERMATOSIS - REPORT OF 6 CASES AND REVIEW OF THE LITERATURE [J].
KUECHLE, MK ;
STEGEMEIR, E ;
MAYNARD, B ;
GIBSON, LE ;
LEIFERMAN, KM ;
PETERS, MS .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1994, 30 (02) :187-192
[8]   LAD-1, the linear IgA bullous dermatosis autoantigen, is a novel 120-kDa anchoring filament protein synthesized by epidermal cells [J].
Marinkovich, MP ;
Taylor, TB ;
Keene, DR ;
Burgeson, RE ;
Zone, JJ .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1996, 106 (04) :734-738
[9]   LINEAR IGA BULLOUS DERMATOSIS RELATED TO LITHIUM-CARBONATE [J].
MCWHIRTER, JD ;
HASHIMOTO, K ;
FAYNE, S ;
ITO, K .
ARCHIVES OF DERMATOLOGY, 1987, 123 (09) :1120-1122
[10]   Bullous skin disease: An unusual allergic reaction to vancomycin [J].
Neughebauer, BI ;
Negron, G ;
Pelton, S ;
Plunkett, RW ;
Beutner, EH ;
Magnussen, R .
AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 2002, 323 (05) :273-278