Department of Dermatology, Jena University Hospital Erfurter Straße 35, DE-07743 Jena, Germany.
Acta Derm Venereol. 2018 Mar 13;98(3):310-317. doi: 10.2340/00015555-2841.
Cutaneous pseudolymphoma (CPL) is a reactive polyclonal T- or B-cell lymphoproliferative process. CPL may appear as localized or disseminated skin lesions. While most cases of CPL are idiopathic, they may also occur as a response to, for example, contact dermatitis, arthropod reactions, and bacterial infections. CPL can be classified based on its clinical features, but all variants have similar histopathological patterns of either predominantly B-cell infiltrates, T-cell infiltrates, or mixed T/B-cell infiltrates. The prognosis of CPL is good, but the underlying disease process should be taken into account. If an antigenic stimulus is identified, it should be removed. In patients with idiopathic CPL, a close follow-up control strategy should be adopted. The aim of this systematic review is to summarize all reported treatments for CPL. The review was based on articles from the PubMed database, using the query "skin pseudolymphoma treatment", English and German, about "human" subjects, and published between 1990 and 2015 documenting adequate treatment and/or aetiology. Mainly individual case reports and small case series were found. Treatment options include topical and intralesional agents, systemic agents, and physical modalities. The final part of the review proposes a treatment algorithm for CPL according to each aetiology, based on the literature of the last 25 years. Future research should focus on randomized controlled trials and studies on long-term outcomes, which were not identified in the current review.
皮肤假性淋巴瘤(CPL)是一种反应性多克隆 T 或 B 细胞淋巴增生性疾病。CPL 可表现为局限性或播散性皮肤损害。虽然大多数 CPL 为特发性,但也可作为接触性皮炎、节肢动物反应和细菌感染等的反应而发生。CPL 可根据其临床特征进行分类,但所有变异型均具有相似的组织病理学模式,主要为 B 细胞浸润、T 细胞浸润或混合 T/B 细胞浸润。CPL 的预后良好,但应考虑到潜在的疾病过程。如果确定了抗原刺激,应将其去除。对于特发性 CPL 患者,应采取密切随访控制策略。本系统综述的目的是总结所有报道的 CPL 治疗方法。该综述基于 PubMed 数据库中的文章,使用查询词“skin pseudolymphoma treatment”,英语和德语,关于“human”主题,发表于 1990 年至 2015 年,记录了充分的治疗和/或病因。主要发现为个别病例报告和小病例系列。治疗选择包括局部和皮损内药物、全身药物和物理疗法。综述的最后一部分根据过去 25 年的文献,针对每种病因提出了 CPL 的治疗算法。未来的研究应侧重于随机对照试验和长期结果研究,这些研究在本次综述中未被确定。