Department of Dermatology, INSERM U1065 Team 12, University Hospital of Nice, Nice, France.
JAMA Dermatol. 2013 Jun;149(6):675-7. doi: 10.1001/jamadermatol.2013.1989.
Interferon alfa remains the central treatment for chronic hepatitis C virus (HCV) infection. Cases of cutaneous and mucous hyperpigmentations during interferon alfa treatment have been reported, but they are considered rare adverse effects.
To study the clinical presentation and frequency of hyperpigmentation in patients receiving interferon alfa treatment for chronic HCV infection.
Prospective, descriptive clinical trial.
Monocentric study performed in the Departments of Hepatology and Dermatology of the University Hospital of Nice, Nice, France.
Consecutive patients treated with pegylated interferon alfa-2b and ribavirin for chronic HCV infection.
Demographic data and medical history were noted. A systematic clinical and dermoscopic examination of skin, nails, and mucous membranes was performed, and skin biopsies were performed if needed.
Of 77 patients who were included, 16 (21%) presented with hyperpigmentation. Hyperpigmentation of the oral mucous membrane, acquired longitudinal melononychia, and hyperpigmentation of the face were each observed in 7 patients (9%). All patients with hyperpigmentation of the skin had skin type III or IV and worked outside without sun protection. The intensity of pigmentation was reported to decrease progressively when interferon treatment was discontinued. Most patients with hyperpigmentation of the oral mucosa also had melanonychia. However, patients with hyperpigmentation of the skin did not have mucosal or nail involvement, suggesting 2 distinct mechanisms.
Secondary hyperpigmentation during interferon alfa treatment occurs as an adverse event in 21% of patients, especially in those with dark skin types who have unprotected sun exposure. Physicians should be aware of the adverse effects of interferon treatment and advise patients in the use of sun protection, especially patients with darker skin types.
干扰素 α 仍然是慢性丙型肝炎病毒(HCV)感染的主要治疗方法。在干扰素 α 治疗期间,已报告有皮肤和黏膜色素沉着过度的病例,但这些病例被认为是罕见的不良反应。
研究接受干扰素 α 治疗慢性 HCV 感染的患者色素沉着过度的临床表现和频率。
前瞻性、描述性临床试验。
法国尼斯大学附属医院肝病科和皮肤科的单中心研究。
连续接受聚乙二醇干扰素 α-2b 和利巴韦林治疗慢性 HCV 感染的患者。
记录人口统计学数据和病史。对皮肤、指甲和黏膜进行系统的临床和皮肤镜检查,如果需要,进行皮肤活检。
在纳入的 77 例患者中,有 16 例(21%)出现色素沉着过度。有 7 例(9%)患者出现口腔黏膜色素沉着、获得性纵向黑甲和面部色素沉着过度。所有皮肤色素沉着过度的患者皮肤类型均为 III 或 IV 型,且在户外工作且无防晒措施。当停止干扰素治疗时,色素沉着的强度被报告逐渐降低。大多数口腔黏膜色素沉着过度的患者也有黑甲。然而,皮肤色素沉着过度的患者没有黏膜或指甲受累,这表明存在两种不同的机制。
在干扰素 α 治疗期间发生的继发性色素沉着过度是 21%患者的不良反应,尤其是那些未进行防晒且皮肤类型较深的患者。医生应注意干扰素治疗的不良反应,并建议患者使用防晒措施,尤其是皮肤类型较深的患者。