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米诺环素诱导的色素沉着:3 种 Q 开关激光逆转其效果的比较。

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

机构信息

Northeast Ohio Medical University, Rootstown, OH, USA.

出版信息

Clin Cosmet Investig Dermatol. 2013 May 31;6:159-62. doi: 10.2147/CCID.S42166. Print 2013.

Abstract

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.

摘要

米诺环素是一种四环素衍生物抗生素,通常用于治疗痤疮、酒渣鼻和其他炎症性皮肤疾病。米诺环素被氧化时会变成黑色,导致皮肤、指甲、球结膜、口腔黏膜、牙齿、骨骼和甲状腺变色。长期使用至少 100 毫克/天的米诺环素治疗后,已报告出现色素沉着。米诺环素可引起三种类型的皮肤色素沉着过度。I 型最常见,与先前炎症和瘢痕部位的蓝黑色变色有关。II 型最常见于腿部,表现为先前正常皮肤的蓝灰色色素沉着。III 型最不常见,特征为弥漫性污浊的棕褐色变色,主要见于暴露于阳光的皮肤。米诺环素诱导的色素沉着可能会影响美观,因此及早识别至关重要。如果不治疗,停药后症状可能需要数月至数年才能缓解。然而,色素沉着可能永远不会完全消失。实际上,很少有报道称任何治疗干预都能完全解决。我们报告了一例长期使用米诺环素治疗的患者,将其用作抗炎药来控制类风湿关节炎的症状,导致米诺环素诱导的面部色素沉着过度。为了去除蓝灰色的皮肤沉积物,在测试区域使用了 3 种 Q 开关激光器(钕:钇铝石榴石(Nd:YAG)1064nm、紫翠玉 755nm 和红宝石 694nm)。紫翠玉 755nm 激光被证明能有效清除米诺环素色素沉着过度,仅需 2 次治疗,治疗不适感和停机时间都最小。

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