2020
DOI: 10.1001/jamadermatol.2020.1069
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The Search for a Uniformly Effective Treatment in Patients With Lupus Miliaris Disseminatus Faciei

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Cited by 3 publications
(4 citation statements)
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“…In recent years, apremilast, a phosphodiesterase 4 inhibitor that downregulates pro-inflammatory mediators (tumor necrosis factor, interferon γ, and interleukins IL2, IL12, and IL23), has shown to be an emerging therapeutic option with reported clinical improvement within four weeks [9]. TNF inhibitor infliximab was also recently reported to be effective in refractory acne agminata, suggesting the role of TNF and Th1-driven IFN gamma pathways as treatment targets for refractory cases [10].…”
Section: Case Discussionmentioning
confidence: 99%
“…In recent years, apremilast, a phosphodiesterase 4 inhibitor that downregulates pro-inflammatory mediators (tumor necrosis factor, interferon γ, and interleukins IL2, IL12, and IL23), has shown to be an emerging therapeutic option with reported clinical improvement within four weeks [9]. TNF inhibitor infliximab was also recently reported to be effective in refractory acne agminata, suggesting the role of TNF and Th1-driven IFN gamma pathways as treatment targets for refractory cases [10].…”
Section: Case Discussionmentioning
confidence: 99%
“…4,5 Reports of effective immunomodulatory treatment corroborate an immune-related pathogenesis. 6 The exact pathophysiology of the disease remains unclear, contributing to unsatisfactory treatment regimens. Some case reports have highlighted success with topical dapsone, 7 a combination of isotretinoin and steroids, 8 intralesional steroids, 9 oral apremilast (three cases) 6 and oral tranilast.…”
Section: Reportmentioning
confidence: 99%
“…6 The exact pathophysiology of the disease remains unclear, contributing to unsatisfactory treatment regimens. Some case reports have highlighted success with topical dapsone, 7 a combination of isotretinoin and steroids, 8 intralesional steroids, 9 oral apremilast (three cases) 6 and oral tranilast. 10 However, many agents are not reliably useful, and the self-limiting nature and rarity of the disease makes conducting clinical trials and evaluating treatment efficacy difficult.…”
Section: Reportmentioning
confidence: 99%
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