波纳替尼治疗后继发的红斑性鱼鳞状糠疹:病例报告及文献复习。

Ariel E Eber, Alyx Rosen, Kate E Oberlin, Alessio Giubellino, Paolo Romanelli
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引用次数: 17

摘要

酪氨酸激酶抑制剂作为多种恶性肿瘤的靶向治疗已经彻底改变了化疗领域。它们比传统化疗更具选择性,通常引起更少的全身不良事件,但毒性仍然存在。皮肤毒性是常见的,他们的管理提出了一个新的挑战,医生和患者。Ponatinib是第三代酪氨酸激酶抑制剂,越来越多的报道引起皮肤皮疹。一名50岁女性,有慢性骨髓性白血病病史,有4个月萎缩性和鱼鳞状粉红色斑块恶化史,累及腋窝、大腿和腹部;脸颊和前额也有红色斑块。由于疾病对先前的治疗包括干扰素、伊马替尼、达沙替尼和博舒替尼难以治愈,她在5个月前开始使用第三代波纳替尼。皮肤活检显示滤泡周围纤维化,角化不全和角化不全交替发生,血管周围淋巴细胞浸润稀疏,符合红斑糠疹样毛毛样反应。开始使用局部维甲酸0.025%乳膏,在3周内消退,没有停止使用波纳替尼。对先前报告的回顾发现了波纳替尼诱导的药物反应之间的显着相似性。在这里,我们强调的不仅是皮肤皮疹发生在波纳替尼治疗,但皮肤的表现是特征性的和独特的,并受益于类维甲酸治疗,而不需要中断重要的化疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ichthyosiform Pityriasis Rubra Pilaris-Like Eruption Secondary to Ponatinib Therapy: Case Report and Literature Review.

Ichthyosiform Pityriasis Rubra Pilaris-Like Eruption Secondary to Ponatinib Therapy: Case Report and Literature Review.

Ichthyosiform Pityriasis Rubra Pilaris-Like Eruption Secondary to Ponatinib Therapy: Case Report and Literature Review.

Tyrosine kinase inhibitors have revolutionized the chemotherapy arena as targeted therapies for a multitude of malignancies. They are more selective than conventional chemotherapy, and often elicit fewer systemic adverse events, however toxicities still exist. Cutaneous toxicities are common and their management presents a novel challenge to physicians and patients. Ponatinib is a third-generation tyrosine kinase inhibitor increasingly reported to cause cutaneous eruption. A 50-year-old woman with a history of chronic myelogenous leukemia presented with a 4-month history of worsening atrophic and ichthyosiform pink plaques involving the axillae, thighs and abdomen; red patches were also observed on the cheeks and forehead. She was started on the third-generation, ponatinib, 5 months earlier because of disease refractory to previous therapies including interferon, imatinib, dasatinib and bosutinib. A skin biopsy revealed perifollicular fibrosis, alternating orthokeratosis and parakeratosis, and a sparse perivascular lymphocytic infiltrate consistent with a pityriasis rubra pilaris-like reaction. Topical tretinoin 0.025% cream was initiated, resulting in resolution within 3 weeks without discontinuation of ponatinib. A review of previous reports identified significant similarities among the ponatinib-induced drug reactions. Here, we highlight not only that cutaneous eruptions occur on ponatinib therapy, but that the dermatologic manifestations are characteristic and unique, and benefit from retinoid therapy, without requiring interruption of vital chemotherapy.

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