Cutaneous Drug Eruptions 2015
DOI: 10.1007/978-1-4471-6729-7_5
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Morbilliform Drug Eruptions

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Cited by 4 publications
(16 citation statements)
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“…The pathophysiology of MDE eruptions is incompletely understood and may vary by patient and drug. Most agree that MDE represents idiosyncratic, T-cell-mediated Type IV delayed-hypersensitivity reactions [ 7 , 9 ]. In some cases, antigen-presenting cells present drug haptens—a drug or drug metabolite bound to a larger carrier protein or peptide—to antigen-specific naive CD4+ and CD8+ T-cells [ 9 , 10 ].…”
Section: Pathophysiologymentioning
confidence: 99%
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“…The pathophysiology of MDE eruptions is incompletely understood and may vary by patient and drug. Most agree that MDE represents idiosyncratic, T-cell-mediated Type IV delayed-hypersensitivity reactions [ 7 , 9 ]. In some cases, antigen-presenting cells present drug haptens—a drug or drug metabolite bound to a larger carrier protein or peptide—to antigen-specific naive CD4+ and CD8+ T-cells [ 9 , 10 ].…”
Section: Pathophysiologymentioning
confidence: 99%
“…In some cases, antigen-presenting cells present drug haptens—a drug or drug metabolite bound to a larger carrier protein or peptide—to antigen-specific naive CD4+ and CD8+ T-cells [ 9 , 10 ]. This interaction induces a complex immune response involving immune cell proliferation, infiltration of the skin, production of inflammatory mediators (both type I and type II cytokines), and induction of cytotoxicity upon exposure to a drug-protein antigen deposited in the skin [ 7 , 11 , 12 , 13 ]. Alternatively, in the p-i (“pharmacologic interaction of drugs with immune receptors”) theory, drugs may trigger an immune response by direct, off-target interaction with immune receptors such as T-cell receptors (TCRs) or major histocompatibility complexes (MHCs) [ 7 , 10 ].…”
Section: Pathophysiologymentioning
confidence: 99%
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“…Classically, these eruptions appear 5 to 14 days after the initiation of the offending agent. 1 On histopathologic examination, dermal hypersensitivity reactions are characterized by a superficial perivascular lymphocytic infiltrate, often with admixed eosinophils. 2 We report an unusual case of a bullous drug reaction, histologically characterized by leukemic cells in a patient with new-onset acute myeloid leukemia (AML).…”
Section: Introductionmentioning
confidence: 99%