Drug-elicited systemic allergic (contact) dermatitis - update and possible pathomechanisms

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Drug-elicited systemic allergic (contact) dermatitis - update and possible pathomechanisms. / Maibach, H.I.; Thyssen, Jacob Pontoppidan.

In: Contact Dermatitis, Vol. 59, No. 4, 2008, p. 195-202.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Maibach, HI & Thyssen, JP 2008, 'Drug-elicited systemic allergic (contact) dermatitis - update and possible pathomechanisms', Contact Dermatitis, vol. 59, no. 4, pp. 195-202.

APA

Maibach, H. I., & Thyssen, J. P. (2008). Drug-elicited systemic allergic (contact) dermatitis - update and possible pathomechanisms. Contact Dermatitis, 59(4), 195-202.

Vancouver

Maibach HI, Thyssen JP. Drug-elicited systemic allergic (contact) dermatitis - update and possible pathomechanisms. Contact Dermatitis. 2008;59(4):195-202.

Author

Maibach, H.I. ; Thyssen, Jacob Pontoppidan. / Drug-elicited systemic allergic (contact) dermatitis - update and possible pathomechanisms. In: Contact Dermatitis. 2008 ; Vol. 59, No. 4. pp. 195-202.

Bibtex

@article{ec0dc0b08bfb11de8bc9000ea68e967b,
title = "Drug-elicited systemic allergic (contact) dermatitis - update and possible pathomechanisms",
abstract = "An allergic dermatitis reaction may develop after systemic exposure to a hapten that reaches the skin through haematogenous transport. This condition can be observed with and without previous cutaneous sensitization to the hapten but has traditionally been described following topical exposure. A heterogeneous clinical picture, in combination with limited insight to its pathomechanisms, makes such systemic reactions an area in need of further study. This article summarizes knowledge about systemic dermatitis elicited by drugs, with a special emphasis on possible pathomechanisms. A list of putative pathomechanisms is offered for future research. Literature was examined using PubMed-MEDLINE, EMBASE, Biosis, and Science Citation Index. Based on the literature, it is likely that humoral type 3, delayed-type hypersensitivity, and drug-driven (i.e. p-i concept) reactions are involved. As commonly used terms may be misleading because skin contact is not a prerequisite, we suggest that the term 'systemic allergic dermatitis' should be used in the future Udgivelsesdato: 2008",
author = "H.I. Maibach and Thyssen, {Jacob Pontoppidan}",
note = "Times Cited: 0ReviewEnglishThyssen, J. PGentofte Univ Hosp, Natl Allergy Res Ctr, Dept Dermatol, Ledreborg 40,1, DK-2820 Gentofte, DenmarkCited References Count: 78354ZYBLACKWELL PUBLISHING9600 GARSINGTON RD, OXFORD OX4 2DQ, OXON, ENGLANDOXFORD",
year = "2008",
language = "English",
volume = "59",
pages = "195--202",
journal = "Contact Dermatitis",
issn = "0105-1873",
publisher = "Wiley-Blackwell",
number = "4",

}

RIS

TY - JOUR

T1 - Drug-elicited systemic allergic (contact) dermatitis - update and possible pathomechanisms

AU - Maibach, H.I.

AU - Thyssen, Jacob Pontoppidan

N1 - Times Cited: 0ReviewEnglishThyssen, J. PGentofte Univ Hosp, Natl Allergy Res Ctr, Dept Dermatol, Ledreborg 40,1, DK-2820 Gentofte, DenmarkCited References Count: 78354ZYBLACKWELL PUBLISHING9600 GARSINGTON RD, OXFORD OX4 2DQ, OXON, ENGLANDOXFORD

PY - 2008

Y1 - 2008

N2 - An allergic dermatitis reaction may develop after systemic exposure to a hapten that reaches the skin through haematogenous transport. This condition can be observed with and without previous cutaneous sensitization to the hapten but has traditionally been described following topical exposure. A heterogeneous clinical picture, in combination with limited insight to its pathomechanisms, makes such systemic reactions an area in need of further study. This article summarizes knowledge about systemic dermatitis elicited by drugs, with a special emphasis on possible pathomechanisms. A list of putative pathomechanisms is offered for future research. Literature was examined using PubMed-MEDLINE, EMBASE, Biosis, and Science Citation Index. Based on the literature, it is likely that humoral type 3, delayed-type hypersensitivity, and drug-driven (i.e. p-i concept) reactions are involved. As commonly used terms may be misleading because skin contact is not a prerequisite, we suggest that the term 'systemic allergic dermatitis' should be used in the future Udgivelsesdato: 2008

AB - An allergic dermatitis reaction may develop after systemic exposure to a hapten that reaches the skin through haematogenous transport. This condition can be observed with and without previous cutaneous sensitization to the hapten but has traditionally been described following topical exposure. A heterogeneous clinical picture, in combination with limited insight to its pathomechanisms, makes such systemic reactions an area in need of further study. This article summarizes knowledge about systemic dermatitis elicited by drugs, with a special emphasis on possible pathomechanisms. A list of putative pathomechanisms is offered for future research. Literature was examined using PubMed-MEDLINE, EMBASE, Biosis, and Science Citation Index. Based on the literature, it is likely that humoral type 3, delayed-type hypersensitivity, and drug-driven (i.e. p-i concept) reactions are involved. As commonly used terms may be misleading because skin contact is not a prerequisite, we suggest that the term 'systemic allergic dermatitis' should be used in the future Udgivelsesdato: 2008

M3 - Journal article

VL - 59

SP - 195

EP - 202

JO - Contact Dermatitis

JF - Contact Dermatitis

SN - 0105-1873

IS - 4

ER -

ID: 13860939