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1.
Dermatol Online J ; 25(10)2019 Oct 15.
Article in English | MEDLINE | ID: mdl-31735009

ABSTRACT

Hydroxyurea is a chemotherapeutic agent that is used in the treatment of various hematological diseases including chronic myelogenous leukemia, polycythemia vera, and sickle cell anemia. Hydroxyurea is also used to treat psoriasis. Drug-induced hyperpigmentation is a known cutaneous side effect of hydroxyurea along with xerosis, dermal ulcers, and dermatomyositis-like eruptions. Hyperpigmentation has been observed in the oral mucosa, nails, and in a generalized or a diffuse pattern. The mechanism of hyperpigmentation related to hydroxyurea is believed to be correlated with increased melanin. Classically, clinical types of diffuse hyperpigmentation owing to iron deposition in the dermis have been associated with minocycline and not with hydroxyurea. We report a novel case in which hydroxyurea hyperpigmentation is associated with iron deposition.


Subject(s)
Hydroxyurea/adverse effects , Hyperpigmentation/chemically induced , Iron/analysis , Nucleic Acid Synthesis Inhibitors/adverse effects , Skin/pathology , Aged , Humans , Hyperpigmentation/pathology , Male , Microscopy, Electrochemical, Scanning , Skin/chemistry
2.
Lasers Surg Med ; 48(3): 234-7, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26718463

ABSTRACT

Pigmentation secondary to minocycline ingestion is an uncommon adverse event affecting 3.7-14.8% of treated individuals for which few effective therapies are available. Three patterns of minocycline pigmentation have a characteristic clinical and histological appearance. The pigment composition in each variety is different and occurs at varying skin depths. Accordingly, a tailored approach according to the type of minocycline pigmentation is crucial for treatment success. The purpose of this intervention was to evaluate the efficacy of non-ablative fractional photothermolysis in combination with the Q-switched alexandrite laser for the treatment of type I minocycline pigmentation on the face. A patient with type I minocycline pigmentation was treated with non-ablative 1550-nm fractional photothermolysis followed immediately by 755-nm Q-switched alexandrite laser and then observed clinically to determine the outcome of this modality. The patient was seen in clinic 1 month later following her single treatment session and 100% clearance of all blue facial pigment was observed. Non-ablative fractional photothermolysis in combination with the 755-nm Q-switched alexandrite laser should be considered for treatment of type I minocycline pigmentation.


Subject(s)
Anti-Bacterial Agents/adverse effects , Hyperpigmentation/surgery , Lasers, Solid-State/therapeutic use , Minocycline/adverse effects , Female , Humans , Hyperpigmentation/chemically induced , Middle Aged , Treatment Outcome
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