2015
DOI: 10.1007/978-3-319-16435-9_11
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Pulmonary Effects of Antineoplastic Therapy

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Cited by 2 publications
(7 citation statements)
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“…The respiratory system is particularly susceptible to drug toxicity during childhood due to ongoing physiological development, its rich vascularity and large contact surface area. As summarised in Table 4, the presentation and pathogenesis of injury varies with specific drugs but is generally hypothesised to arise from several key mechanisms: (1) oxidative injury to endothelium and pneumocytes, (2) cytokine induction and inflammation, (3) proteinolytic destruction, (4) immune dysregulation and/or ( 5) idiosyncrasy [35,[55][56][57].…”
Section: Chemotherapymentioning
confidence: 99%
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“…The respiratory system is particularly susceptible to drug toxicity during childhood due to ongoing physiological development, its rich vascularity and large contact surface area. As summarised in Table 4, the presentation and pathogenesis of injury varies with specific drugs but is generally hypothesised to arise from several key mechanisms: (1) oxidative injury to endothelium and pneumocytes, (2) cytokine induction and inflammation, (3) proteinolytic destruction, (4) immune dysregulation and/or ( 5) idiosyncrasy [35,[55][56][57].…”
Section: Chemotherapymentioning
confidence: 99%
“…Pulmonary-toxic chemotherapies can cause acute pulmonary and pleural reactions such as hypersensitivity pneumonitis, pleural effusions and lung infiltrates. Hypersensitivity reactions are most frequently reported with bleomycin and methotrexate and usually manifest as reversible eosinophilic or desquamative interstitial pneumonitis [48,55,58]. However, the most pertinent and concerning pulmonary complications of chemotherapy are interstitial pneumonitis and permanent fibrosis.…”
Section: Chemotherapymentioning
confidence: 99%
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