Hodak Emmilia, Amitay-Laish Iris, Bagot Martine, Battistella Maxime, Ben Amitai Dan, Cozzio Antonio, Duvic Madeleine, Ferenczi Katalin, Foss Francine, Geskin Larisa, Guenova Emmanuella, Kim Youn H, Koh Mark Jean-Aan, Molgó Montserrat, Nanda Arti, Nicolay Jan P, Niehues Tim, Ortiz-Romero Pablo, Osmancevic Amra, Papadavid Evangelia, Park Jong Bin, Quaglino Pietro, Sanches José A, Scarisbrick Julia, Sulis Maria Luisa, Stadler Rudolf, Trautinger Franz, Vermeer Maarten, Wohlmuth Iris, Zic John A, Assaf Chalid
Division of Oncology, Davidoff Medical Center, Rabin Medical Center, Beilinson Hospital, Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Division of Dermatology, Rabin Medical Center, Beilinson Hospital, Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Br J Dermatol. 2025 Aug 18;193(3):405-414. doi: 10.1093/bjd/ljaf199.
Mycosis fungoides (MF) is considered rare in children and adolescents. Accumulating experience indicates that compared with adult patients, almost all paediatric patients with MF are diagnosed at an early stage of disease, exhibit higher rates of atypical presentations and follow a notably indolent course. Despite the need for special staging/investigations specific for children and adolescents, the staging of paediatric MF is currently based primarily on standard practice in adults. The aim of this work was to develop staging recommendations specifically designed for MF in children and adolescents, on behalf of the three largest societies for cutaneous lymphomas, the International Society for Cutaneous Lymphomas, the European Organisation for Research and Treatment of Cancer - Cutaneous Lymphoma Tumor Group, and the United States Cutaneous Lymphoma Consortium. We developed this guideline through an international expert consensus process and in accordance with the EQUATOR Network's recommendations for guideline development. A modified Delphi process was conducted, using questionnaires covering topics including the definition, characteristics and staging of paediatric MF. Two rounds of expert feedback were conducted, with an additional hybrid consensus meeting. We reached a consensus that the term 'paediatric MF' should be reserved for MF diagnosed at ≤ 18 years of age. Panellists specified the unique clinical characteristics of paediatric MF, including a high prevalence of hypopigmented and folliculotropic variants, and reached a consensus on the indolent nature of the disease during childhood and adolescence with rare progression to advanced stage. The consensus reached recommends that while the staging approach is largely similar to that in adults, imaging for early-stage paediatric MF should rely on ultrasound of the lymph nodes if indicated, rather than computed tomography with contrast or integrated with positron emission tomography. Along with this, clinicians should be aware that in children, palpable lymph nodes are common owing to the increased incidence of infectious diseases. In summary, this guideline addresses the major clinical characteristics of paediatric MF, which differ from those in adults, and provides practical staging recommendations considering the safety implications specific for this age group.
蕈样肉芽肿(MF)在儿童和青少年中被认为较为罕见。越来越多的经验表明,与成年患者相比,几乎所有儿童MF患者在疾病早期被诊断,非典型表现发生率更高,病程明显惰性。尽管需要针对儿童和青少年的特殊分期/检查,但目前儿童MF的分期主要基于成人的标准做法。这项工作的目的是代表三个最大的皮肤淋巴瘤协会,即国际皮肤淋巴瘤协会、欧洲癌症研究与治疗组织 - 皮肤淋巴瘤肿瘤组和美国皮肤淋巴瘤联盟,制定专门针对儿童和青少年MF的分期建议。我们通过国际专家共识过程并按照EQUATOR网络关于指南制定的建议制定了本指南。采用了改良的德尔菲法,使用涵盖儿童MF定义、特征和分期等主题的问卷。进行了两轮专家反馈,并额外召开了一次混合共识会议。我们达成共识,“儿童MF”一词应保留用于18岁及以下诊断的MF。小组成员明确了儿童MF的独特临床特征,包括色素减退和毛囊性变体的高患病率,并就该疾病在儿童期和青少年期的惰性性质以及罕见进展至晚期达成共识。达成的共识建议,虽然分期方法在很大程度上与成人相似,但对于早期儿童MF,如果有指征,成像应依赖淋巴结超声,而不是增强计算机断层扫描或与正电子发射断层扫描联合。与此同时,临床医生应意识到,在儿童中,由于传染病发病率增加,可触及的淋巴结很常见。总之,本指南阐述了儿童MF与成人不同的主要临床特征,并考虑到该年龄组特有的安全问题提供了实用的分期建议。