[博来霉素继发鞭毛状红斑:1例报告,预后良好]。

Ricardo Leal-León, Antonio Tirado-Motel, Marian Escribano-Ponce, Vanessa González-Ruiz, María Teresa de Jesús Vega-González
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引用次数: 0

摘要

背景:鞭毛性红斑(FE)是一种多因素皮肤病,常与某些药物的使用有关。在接受博来霉素治疗的患者中,高达20%的患者会出现这种情况。药物在皮肤中的积累可能是由于缺乏酶博来霉素水解酶。它表现为一种广泛的皮肤病,主要累及躯干和上肢,特征为大小不一的红斑色素沉着,呈线状排列,呈“鞭子状”外观,伴有强烈瘙痒。治疗的重点是用抗组胺药和局部类固醇缓解瘙痒,尽管停止博来霉素是完全解决的必要条件。病例报告:一名19岁女性,患有IIIB期左卵巢异常生殖细胞瘤,正在接受联合化疗(博来霉素、依托泊苷和顺铂)。治疗3个月后,患者在颈部和胸后区域出现广泛的皮肤病,包括线性形状和大小不等的深棕色色素沉着斑,伴有瘙痒,无其他症状。诊断为博来霉素所致FE。开了高效外用皮质类固醇。停用博来霉素后,皮肤病逐渐消失,直至完全消退。结论:博来霉素引起的FE必须及早发现,以便进行适当的治疗,从而继续进行抗肿瘤治疗。当患者的生活质量受到损害并与肿瘤控制相平衡时,应考虑停药,从而优化抗肿瘤治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Flagellate erythema secondary to bleomycin: case report with favorable outcome].

Background: Flagellate erythema (FE) is a multifactorial dermatosis, frecuently related to the the use of certain drugs. It can occur in up to 20% of patients treated with bleomycin. Drug accumulation in the skin can be due to the lack of the enzyme bleomycin hydrolase. It presents as a widespread dermatosis, predominantly affecting the trunk and upper extremities, characterized by erythematous-hyperpigmented macules of variable size, with a linear arrangement and a "whip-like" appearance, associated with intense pruritus. Management focuses on relieving pruritus with antihistamines and topical steroids, although discontinuation of bleomycin is essential for complete resolution.

Case report: A 19-year-old woman with a history of stage IIIB left ovarian dysgerminoma was undergoing combined chemotherapy (bleomycin, etoposide, and cisplatin). After 3 months of treatment, she developed a widespread dermatosis on the neck and posterior thoracic region, consisting of dark brown hyperpigmented spots with a linear configuration and variable sizes, associated with pruritus, without other symptoms. FE due to bleomycin was diagnosed. High-potency topical corticosteroids were prescribed. After discontinuing bleomycin, there was a progressive disappearance of the dermatosis until complete resolution.

Conclusion: The bleomycin-induced FE must be identified early for appropriate management that allows the continuation of antineoplastic treatment. Discontinuation of the drug should be considered when the patient's quality of life is compromised and balanced with oncological control, which optimizes antineoplastic therapy.

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