Suppr超能文献

解读皮肤组织细胞增多症:对组织学、发病机制、诊断及治疗陷阱的见解

Unraveling cutaneous histiocytosis: insights into histology, pathogenesis, diagnosis, and treatment pitfalls.

作者信息

Scurtu Lucian G, Scurtu Francesca, Simionescu Olga

机构信息

Faculty of Medicine, "Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania.

Department of Dermatology I, Colentina Clinical Hospital, Bucharest, Romania.

出版信息

Front Med (Lausanne). 2025 Jun 20;12:1585815. doi: 10.3389/fmed.2025.1585815. eCollection 2025.

Abstract

Histiocytoses represent a group of diverse rare disorders characterized by the abnormal accumulation of cells derived from the mononuclear phagocyte system in various tissues and organs. The mononuclear phagocyte system includes monocytes, macrophages, dendritic cells, and specialized tissue-resident phagocytes. These cells are essential for both innate and adaptive immunity and preserving tissue homeostasis. Several classifications of histiocytoses by the Histiocyte Society (1987, 1997, 2016) and WHO (2018, 2022) and an International Consensus Classification (2022) are generally acknowledged. The WHO 2022 classification clarifies these heterogeneous disorders by dividing them into three major groups. Cutaneous involvement in histiocytosis is often polymorphous, making clinical decision more challenging. Cutaneous histiocytoses can occur either as primary cases or as a manifestation of a multisystemic disease. In support of the standard pathology report, immunohistochemical staining is warranted. The exact etiopathogenesis of histiocytoses remains poorly understood, and various associations with malignancies, including visceral and hematologic cancers, as well as autoimmune diseases and infections (Borrelia burgdorferi) are still under review. One of the most recent advancements in this field is the discovery of somatic mutations in the RAF-MEK-ERK signaling pathway, particularly BRAF mutations. Oncogene-induced senescence-associated BRAF mutations have been described in Langerhans cell histiocytosis and Erdheim-Chester disease. Targeted therapies with BRAF inhibitors such as dabrafenib and vemurafenib have shown promising results. MEK inhibitors, like trametinib and cobimetinib, have demonstrated efficiency regardless of the BRAF mutation status. Local treatments of cutaneous histiocytosis include topical steroids, calcineurin inhibitors, alkylating agents, phototherapy, steroid injections, and laser therapies. Despite the current advances in pathogenesis and treatments, cutaneous histiocytosis stands as a challenging and heterogeneous group of disorders, and treatment guidelines are warranted.

摘要

组织细胞增多症是一组罕见的、多样的疾病,其特征是源自单核吞噬细胞系统的细胞在各种组织和器官中异常积聚。单核吞噬细胞系统包括单核细胞、巨噬细胞、树突状细胞和特殊的组织驻留吞噬细胞。这些细胞对于先天免疫和适应性免疫以及维持组织稳态至关重要。组织细胞增多症的几种分类由组织细胞协会(1987年、1997年、2016年)、世界卫生组织(2018年、2022年)以及国际共识分类(2022年)给出,这些分类已得到普遍认可。世界卫生组织2022年的分类通过将这些异质性疾病分为三大组,使其更加清晰明了。组织细胞增多症中的皮肤受累通常具有多形性,这使得临床决策更具挑战性。皮肤组织细胞增多症既可以作为原发性病例出现,也可以作为多系统疾病的一种表现。为了支持标准病理报告,免疫组化染色是必要的。组织细胞增多症的确切病因发病机制仍知之甚少,与包括内脏和血液系统癌症在内的恶性肿瘤以及自身免疫性疾病和感染(伯氏疏螺旋体)的各种关联仍在研究之中。该领域最近的进展之一是在RAF-MEK-ERK信号通路中发现了体细胞突变,特别是BRAF突变。在朗格汉斯细胞组织细胞增多症和厄尔德海姆-切斯特病中已经描述了致癌基因诱导的衰老相关BRAF突变。使用达拉非尼和维莫非尼等BRAF抑制剂的靶向治疗已显示出有前景的结果。如曲美替尼和考比替尼等MEK抑制剂,无论BRAF突变状态如何,都已证明有效。皮肤组织细胞增多症的局部治疗包括外用类固醇、钙调神经磷酸酶抑制剂、烷化剂、光疗、类固醇注射和激光治疗。尽管目前在发病机制和治疗方面取得了进展,但皮肤组织细胞增多症仍然是一组具有挑战性的异质性疾病,因此有必要制定治疗指南。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验