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Minocycline-induced hyperpigmentation: comparison of 3 Q-switched lasers to reverse its effects

Minocycline is a tetracycline derivative antibiotic commonly prescribed for acne, rosacea, and other inflammatory skin disorders. Minocycline turns black when oxidized, leading to discoloration of the skin, nails, bulbar conjunctiva, oral mucosa, teeth, bones, and thyroid gland. Hyperpigmentation ha...

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Autores principales: Nisar, Mahrukh S, Iyer, Karthik, Brodell, Robert T, Lloyd, Jenifer R, Shin, Thuzar M, Ahmad, Asad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674755/
https://www.ncbi.nlm.nih.gov/pubmed/23754872
http://dx.doi.org/10.2147/CCID.S42166
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author Nisar, Mahrukh S
Iyer, Karthik
Brodell, Robert T
Lloyd, Jenifer R
Shin, Thuzar M
Ahmad, Asad
author_facet Nisar, Mahrukh S
Iyer, Karthik
Brodell, Robert T
Lloyd, Jenifer R
Shin, Thuzar M
Ahmad, Asad
author_sort Nisar, Mahrukh S
collection PubMed
description Minocycline is a tetracycline derivative antibiotic commonly prescribed for acne, rosacea, and other inflammatory skin disorders. Minocycline turns black when oxidized, leading to discoloration of the skin, nails, bulbar conjunctiva, oral mucosa, teeth, bones, and thyroid gland. Hyperpigmentation has been reported after long-term minocycline therapy with at least 100 mg/day. Three types of minocycline-induced cutaneous hyperpigmentation can result. Type I is the most common, and is associated with blue-black discoloration in areas of previous inflammation and scarring. Type II most commonly affects the legs and is characterized by blue-gray pigmentation of previously normal skin. Type III is the least common and is characterized by diffuse muddy-brown discoloration predominantly on sun exposed skin. Minocycline-induced hyperpigmentation may be cosmetically disfiguring and prompt identification is essential. Without treatment, symptoms may take several months, to years to resolve, after discontinuation of the drug. However, the pigmentation may never completely disappear. In fact, there have been few reports of complete resolution associated with any therapeutic intervention. We report a case of a patient on long-term minocycline therapy utilized as an anti-inflammatory agent to control symptoms of rheumatoid arthritis, which led to minocycline-induced hyperpigmentation of the face. To remove the blue-gray cutaneous deposits, 3 Q-switched lasers (Neodymium: yttrium aluminum garnet (Nd:YAG) 1064 nm, Alexandrite 755 nm, and Ruby 694 nm) were used in test areas. The Alexandrite 755 nm laser proved to provide effective clearing of the minocycline hyperpigmentation requiring just 2 treatments, with minimal treatment discomfort and down time.
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spelling pubmed-36747552013-06-10 Minocycline-induced hyperpigmentation: comparison of 3 Q-switched lasers to reverse its effects Nisar, Mahrukh S Iyer, Karthik Brodell, Robert T Lloyd, Jenifer R Shin, Thuzar M Ahmad, Asad Clin Cosmet Investig Dermatol Case Report Minocycline is a tetracycline derivative antibiotic commonly prescribed for acne, rosacea, and other inflammatory skin disorders. Minocycline turns black when oxidized, leading to discoloration of the skin, nails, bulbar conjunctiva, oral mucosa, teeth, bones, and thyroid gland. Hyperpigmentation has been reported after long-term minocycline therapy with at least 100 mg/day. Three types of minocycline-induced cutaneous hyperpigmentation can result. Type I is the most common, and is associated with blue-black discoloration in areas of previous inflammation and scarring. Type II most commonly affects the legs and is characterized by blue-gray pigmentation of previously normal skin. Type III is the least common and is characterized by diffuse muddy-brown discoloration predominantly on sun exposed skin. Minocycline-induced hyperpigmentation may be cosmetically disfiguring and prompt identification is essential. Without treatment, symptoms may take several months, to years to resolve, after discontinuation of the drug. However, the pigmentation may never completely disappear. In fact, there have been few reports of complete resolution associated with any therapeutic intervention. We report a case of a patient on long-term minocycline therapy utilized as an anti-inflammatory agent to control symptoms of rheumatoid arthritis, which led to minocycline-induced hyperpigmentation of the face. To remove the blue-gray cutaneous deposits, 3 Q-switched lasers (Neodymium: yttrium aluminum garnet (Nd:YAG) 1064 nm, Alexandrite 755 nm, and Ruby 694 nm) were used in test areas. The Alexandrite 755 nm laser proved to provide effective clearing of the minocycline hyperpigmentation requiring just 2 treatments, with minimal treatment discomfort and down time. Dove Medical Press 2013-05-31 /pmc/articles/PMC3674755/ /pubmed/23754872 http://dx.doi.org/10.2147/CCID.S42166 Text en © 2013 Nisar et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Case Report
Nisar, Mahrukh S
Iyer, Karthik
Brodell, Robert T
Lloyd, Jenifer R
Shin, Thuzar M
Ahmad, Asad
Minocycline-induced hyperpigmentation: comparison of 3 Q-switched lasers to reverse its effects
title Minocycline-induced hyperpigmentation: comparison of 3 Q-switched lasers to reverse its effects
title_full Minocycline-induced hyperpigmentation: comparison of 3 Q-switched lasers to reverse its effects
title_fullStr Minocycline-induced hyperpigmentation: comparison of 3 Q-switched lasers to reverse its effects
title_full_unstemmed Minocycline-induced hyperpigmentation: comparison of 3 Q-switched lasers to reverse its effects
title_short Minocycline-induced hyperpigmentation: comparison of 3 Q-switched lasers to reverse its effects
title_sort minocycline-induced hyperpigmentation: comparison of 3 q-switched lasers to reverse its effects
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674755/
https://www.ncbi.nlm.nih.gov/pubmed/23754872
http://dx.doi.org/10.2147/CCID.S42166
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