Department of Dermatology, Penn State Milton S. Hershey Medical Center, USA.
Keystone Dermatology and Center for Skin Surgery, Altoona, Pennsylvania, USA.
Cutis. 2020 Aug;106(2):E8-E11. doi: 10.12788/cutis.0074.
This case series discusses 3 patients with long-standing eczematous or psoriasiform dermatitis, demonstrated by multiple biopsies. Following off-label treatment with dupilumab, all 3 patients had clinical expansion of disease, with histopathologic features consistent with cutaneous T-cell lymphoma (CTCL) on subsequent biopsy. We postulate that this expansion likely was secondary to an exacerbation of extant CTCL following exposure to dupilumab. A proposed mechanism of promotion of CTCL is based on the functional increase in IL-13 available for binding at the upregulated IL-13 receptor (IL-13R) α2 site on cells, following blockade of the α1 receptor with dupilumab. This progression merits further investigation.
本病例系列讨论了 3 例患有长期湿疹样或银屑病样皮炎的患者,这些患者通过多次活检得到证实。在接受达必妥(dupilumab)的标签外治疗后,所有 3 例患者的疾病均出现临床扩展,随后的活检显示组织病理学特征与皮肤 T 细胞淋巴瘤(CTCL)一致。我们推测,这种扩展可能是由于在接触达必妥后,现有的 CTCL 恶化所致。CTCL 促进的一个假设机制是基于在阻断 α1 受体后,IL-13 受体 (IL-13R) α2 位点上可用于结合的 IL-13 功能增加,IL-13 可结合细胞上上调的 IL-13R α2 位点。这种进展值得进一步研究。