Jensen Anders Bisgaard, Stausbøl-Grøn Birgitte, Riber-Hansen Rikke, d'Amore Francesco
Department of Hematology, Aarhus University Hospital, Aarhus, Denmark.
Department of Dermatology, Aarhus University Hospital, Aarhus, Denmark.
Dermatol Reports. 2017 Apr 20;9(1):6976. doi: 10.4081/dr.2017.6976. eCollection 2017 Mar 13.
Waldenstrom's macroglobulinamia (WM) is a rare malignant lymphoproliferative disorder, characterized by monoclonal IgM paraproteinemia and neoplastic proliferation of malignant lymphoplasmacytoid cells in the bone marrow. Traditionally, WM has been treated with modalities similar to those used in the management of other indolent lymphomas. Just recently, based on impressive clinical trial results in heavily pretreated WM patients, a new Bruton Tyrosine Kinase-inhibitor, Ibrutinib, has been approved for the treatment of this disorder. As the use of Ibrutinib in WM outside clinical trials is still limited, only few clinical reports illustrating treatment side effects are currently available. Here we review the current literature specific on Ibrutinib-associated rash in hematologic patients, and report on an elderly patient with WM, who developed a red maculopapular non-pruritic rash 12 weeks after starting Ibrutinib therapy. Without modifications of the ongoing Ibrutinib schedule, the rash regressed within two weeks of treatment with topical steroid-containing dermatological compounds.
华氏巨球蛋白血症(WM)是一种罕见的恶性淋巴增殖性疾病,其特征为单克隆IgM副蛋白血症以及骨髓中恶性淋巴浆细胞样细胞的肿瘤性增殖。传统上,WM的治疗方式与其他惰性淋巴瘤的治疗方式类似。就在最近,基于在经过大量预处理的WM患者中取得的令人印象深刻的临床试验结果,一种新型布鲁顿酪氨酸激酶抑制剂——依鲁替尼,已被批准用于治疗这种疾病。由于依鲁替尼在临床试验之外用于WM的情况仍然有限,目前仅有少数说明治疗副作用的临床报告。在此,我们回顾了当前关于血液学患者中依鲁替尼相关皮疹的文献,并报告了一名患有WM的老年患者,该患者在开始依鲁替尼治疗12周后出现了红色斑丘疹,无瘙痒症状。在未改变正在进行的依鲁替尼治疗方案的情况下,使用含局部类固醇的皮肤科化合物治疗两周后皮疹消退。