1987
DOI: 10.1016/0016-5085(87)90925-5
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Isotretinoin-associated proctosigmoiditis

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Cited by 58 publications
(23 citation statements)
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“…Animal studies have indicated that excessive intake of retinoids can have inhibitory effects on both osteoblast and osteoclast activity that may pose a theoretical risk for fractures or hyperostosis. [99][100][101][102][103][104][105][106][107][108][109][110][111][112] Well-designed clinical studies involving human subjects have generated conflicting data on the association between excessive intake of vitamin A with the incidence of fractures. In evaluating isotretinoin specifically, 1 small prospective cohort study associated isotretinoin with minimal-to-mild bone demineralization at specific sites (such as Ward' s triangle of the femur), but revealed that these effects may be reversible.…”
Section: Bone Effectsmentioning
confidence: 99%
“…Animal studies have indicated that excessive intake of retinoids can have inhibitory effects on both osteoblast and osteoclast activity that may pose a theoretical risk for fractures or hyperostosis. [99][100][101][102][103][104][105][106][107][108][109][110][111][112] Well-designed clinical studies involving human subjects have generated conflicting data on the association between excessive intake of vitamin A with the incidence of fractures. In evaluating isotretinoin specifically, 1 small prospective cohort study associated isotretinoin with minimal-to-mild bone demineralization at specific sites (such as Ward' s triangle of the femur), but revealed that these effects may be reversible.…”
Section: Bone Effectsmentioning
confidence: 99%
“…However, there are rare cases that have a strong association between treatment with isotretinoin and exacerbation of inflammatory bowel disease (Martin et al 1987).…”
Section: Other Gastrointestinal Adverse Effectsmentioning
confidence: 99%
“…A similar case has been reported. 29 Musculoskeletal symptoms, defined as any complaint about bones, muscles, or joints, occurred in approxi¬ mately 40% of our subjects, indicating a higher risk than the 15% to 28% risk reported by others.5'7,24 One of the possible explanations for this discrepancy may be that we grouped any muscle, bone, or joint ache or pain into this category, whereas some of the other investiga¬ tors have primarily evaluated "arthralgias." Our data suggest that the risk for musculoskeletal symptoms is increased as the isotretinoin dosage is increased.…”
Section: Resultsmentioning
confidence: 72%