Department of Pediatrics, Japanese Red Cross Otsu Hospital, Otsu, Japan.
Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Pediatr Blood Cancer. 2024 Jul;71(7):e31043. doi: 10.1002/pbc.31043. Epub 2024 Apr 28.
Here, we describe two patients with juvenile xanthogranuloma (JXG) manifesting with Langerhans cell histiocytosis (LCH)-associated neurodegenerative disease (ND)-like radiological findings. One patient showed typical radiological abnormalities at onset, which worsened with progressing central nervous system symptoms 7 years after LCH-oriented chemotherapy. Another showed spontaneous regression of clinical symptoms, with a transient radiological change 1 year after salvage chemotherapy for recurrence of JXG. These data regarding JXG-associated ND will facilitate future investigation of the disease, as well as development of therapeutic interventions.
在这里,我们描述了两例表现为朗格汉斯细胞组织细胞增生症(LCH)相关神经退行性疾病(ND)样影像学表现的幼年黄色肉芽肿(JXG)患者。其中一名患者在发病时表现出典型的影像学异常,在 LCH 为导向的化疗后 7 年,随着中枢神经系统症状的进展,病情恶化。另一名患者在 JXG 复发后接受挽救性化疗 1 年后,临床症状自发缓解,影像学改变短暂。这些关于 JXG 相关 ND 的数据将有助于未来对该疾病的研究,并为治疗干预措施的发展提供依据。