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幼年黄色肉芽肿表现为 LCH 相关的神经退行性疾病样影像学表现。

Juvenile xanthogranuloma manifesting with LCH-associated neurodegenerative disease-like radiological findings.

机构信息

Department of Pediatrics, Japanese Red Cross Otsu Hospital, Otsu, Japan.

Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

出版信息

Pediatr Blood Cancer. 2024 Jul;71(7):e31043. doi: 10.1002/pbc.31043. Epub 2024 Apr 28.

Abstract

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.

摘要

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。

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