Pharmacotherapy. 2011 Sep;31(9):925. doi: 10.1592/phco.31.9.925.
Stevens-Johnson syndrome is a rare, severe cutaneous reaction most often associated with drug therapy. Lenalidomide is a derivative of thalidomide used in the treatment of multiple myeloma. We describe a case of Stevens-Johnson syndrome possibly induced by lenalidomide in a 73-year-old Caucasian female undergoing induction therapy for multiple myeloma. After 13 doses of induction therapy, she was admitted to the hospital directly from her oncologist's office after presenting with a diffuse, bodywide, maculopapular rash with desquamation. She had prominent crusting of her lips, erythematous ulcers on her soft palate that could not be distinguished from petechial hemorrhages, and acute kidney injury (serum creatinine concentration 4.6 mg/dl). She was also febrile and hypotensive. Lenalidomide was discontinued, and the patient was treated with intravenous dexamethasone 10 mg every 6 hours and topical corticosteroids. Over the next week, the patient's condition improved, but she had extensive exfoliation of her rash and pruritus that required antihistamine therapy. By hospital day 9, her rash continued to improve, her pruritus resolved, and she was discharged with a tapering dose of oral prednisone. Lenalidomide was switched to bortezomib for her induction therapy, and the patient did not experience any further cutaneous reactions. The results of a skin biopsy concluded that the findings were consistent with a drug hypersensitivity reaction, suspected to be Stevens-Johnson syndrome. Use of the Naranjo adverse drug reaction probability scale indicated a possible relationship (score of 3) between the patient's development of Stevens-Johnson syndrome and lenalidomide therapy. To our knowledge, no published case reports of severe dermatologic reactions, such as Stevens-Johnson syndrome or toxic epidermal necrolysis, to lenalidomide have been reported. Thus, we believe this to be the first published case report of a patient who developed Stevens-Johnson syndrome while receiving lenalidomide for induction therapy for multiple myeloma. Clinicians should have a heightened awareness of the signs and symptoms of these severe skin reactions if their patients are receiving lenalidomide.
史蒂文斯-约翰逊综合征是一种罕见的严重皮肤反应,最常与药物治疗有关。来那度胺是一种沙利度胺的衍生物,用于治疗多发性骨髓瘤。我们描述了一例 73 岁白人女性在接受多发性骨髓瘤诱导治疗时可能由来那度胺引起的史蒂文斯-约翰逊综合征。在接受 13 剂诱导治疗后,她在从肿瘤医生办公室直接住院,当时她出现了全身弥漫性、斑片状皮疹伴脱屑。她的嘴唇有明显的结痂,软腭上有红斑性溃疡,无法与瘀点出血区分,还有急性肾损伤(血清肌酐浓度 4.6mg/dl)。她还发热和低血压。来那度胺被停用,患者接受了静脉注射地塞米松 10mg,每 6 小时一次,以及局部皮质类固醇治疗。在接下来的一周里,患者的病情有所改善,但她的皮疹广泛脱皮,瘙痒需要抗组胺治疗。到住院第 9 天,她的皮疹继续改善,瘙痒缓解,然后出院时口服泼尼松逐渐减量。来那度胺被换用硼替佐米进行诱导治疗,患者没有再出现皮肤反应。皮肤活检结果表明,这些发现与药物过敏反应一致,疑似史蒂文斯-约翰逊综合征。使用 Naranjo 药物不良反应概率量表表明,患者发生史蒂文斯-约翰逊综合征与来那度胺治疗之间可能存在关系(评分 3)。据我们所知,目前尚无关于来那度胺引起严重皮肤反应(如史蒂文斯-约翰逊综合征或中毒性表皮坏死松解症)的已发表病例报告。因此,我们认为这是首例接受来那度胺诱导治疗多发性骨髓瘤的患者发生史蒂文斯-约翰逊综合征的病例报告。如果患者正在接受来那度胺治疗,临床医生应提高对这些严重皮肤反应的体征和症状的认识。