Wieser Iris, Wang Casey, Alberti-Violetti Silvia, Lyons Genevieve, Tran Casey, Talpur Rakshandra, Duvic Madeleine
Department of Dermatology, MD Anderson Cancer Center, The University of Texas, 1515 Holcombe Blvd, Houston, TX, 77030-4095, USA.
Department of Dermatology, Paracelsus Medical University, Salzburg, Austria.
Arch Dermatol Res. 2017 Aug;309(6):453-459. doi: 10.1007/s00403-017-1744-1. Epub 2017 May 17.
Folliculotropic mycosis fungoides (FMF) is a distinct variant of mycosis fungoides (MF) where atypical T-cells invade the hair follicles. The objective was to assess the clinical features, risk factors for progression, long-term outcome and response to treatment modalities in a large cohort of FMF patients. We, therefore, conducted a single-center retrospective study, reviewing 114 patients with FMF seen from 1987 to 2015 at the cutaneous T-cell lymphoma clinic of the MD Anderson Cancer Center. The mean age at diagnosis of FMF was 57.1 ± 13.5 years. The male to female ratio was 1.2:1. MF stage IA (n = 50, 43.9%) was the most common diagnosed stage, followed equally by stages IB and IIB (n = 23, 20.2%, respectively). Eighty-six patients (75.4%) suffered from pruritus. Concomitant hair loss was observed in 37 (32.5%) subjects. The median number of different treatment modalities used per patient was 4 (range 1-12). Low-dose radiation was beneficial in clearing therapy refractory lesions. The overall survival was influenced by several factors, including advanced age (>65), late stages and the presence of large cell transformation (LCT). Thirty-three of 113 patients (29.2%) progressed to more advanced stages and 26 (23.0%) died, with the cause of death being MF in 11 (9.7%) subjects. In conclusion, patients with FMF have a worse overall 10-year survival rate compared with other MF variants. Several factors, including stage, advanced age and the presence of LCT impact survival. Multiple different treatment approaches may be needed to achieve a good clinical response and to prevent disease progression.
毛囊性蕈样肉芽肿(FMF)是蕈样肉芽肿(MF)的一种独特亚型,其中非典型T细胞侵入毛囊。目的是评估一大群FMF患者的临床特征、病情进展的危险因素、长期预后以及对治疗方式的反应。因此,我们进行了一项单中心回顾性研究,回顾了1987年至2015年在MD安德森癌症中心皮肤T细胞淋巴瘤诊所就诊的114例FMF患者。FMF诊断时的平均年龄为57.1±13.5岁。男女比例为1.2∶1。MF IA期(n = 50,43.9%)是最常见的诊断阶段,其次是IB期和IIB期(均为n = 23,各占20.2%)。86例患者(75.4%)有瘙痒症状。37例(32.5%)患者伴有脱发。每位患者使用的不同治疗方式的中位数为4种(范围为1 - 12种)。低剂量放疗有助于清除治疗难治性病变。总生存受到几个因素的影响,包括高龄(>65岁)、晚期以及大细胞转化(LCT)的存在。113例患者中有33例(29.2%)进展至更晚期,26例(23.0%)死亡,11例(9.7%)患者的死亡原因是MF。总之,与其他MF亚型相比,FMF患者的10年总生存率更差。包括分期、高龄和LCT的存在等几个因素影响生存。可能需要多种不同的治疗方法来获得良好的临床反应并预防疾病进展。