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朗格汉斯细胞组织细胞增多症伴截瘫的放射治疗:1例罕见的婴儿期肿瘤急症病例报告及文献综述

Radiotherapy for Langerhans cell histiocytosis with paraplegia: A rare oncologic emergency case report in infancy and literature review.

作者信息

Nakashima Kentaro, Koga Yuhki, Sakai Yasunari, Takada Hidetoshi, Harimaya Katsumi, Ohga Saiji, Taguchi Tomoaki, Oda Yoshinao, Honda Hiroshi, Ohga Shouichi

机构信息

Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

出版信息

Brain Dev. 2018 Nov;40(10):952-955. doi: 10.1016/j.braindev.2018.05.016. Epub 2018 Jun 12.

DOI:10.1016/j.braindev.2018.05.016
PMID:29907475
Abstract

BACKGROUND

Langerhans cell histiocytosis (LCH) is a clonal disease with focal or disseminated lesions that may compress the surrounding tissues, including the spinal cord. Because few reports have described the spinal symptoms as the first manifestation of pediatric LCH, the long-term neurological outcomes remain unclear.

CASE REPORT AND LITERATURE REVIEW

We report a 21-month-old boy who presented with sudden-onset paraplegia. Imaging analyses revealed that osteolytic lesions and epidural tumors compressing the spinal cord at the T7-9 vertebrae. Twelve days after he developed leg weakness, emergency radiotherapy was started after a tumor biopsy. During the course of radiotherapy, paralysis steadily ameliorated. After we excluded infections and determined the pathological diagnosis of LCH, multi-drug chemotherapy was started. Apparent improvement in his complete paraplegia was observed after a total 15 Gy of radiotherapy and subsequent chemotherapy, leaving no neurological sequelae at 4 years of age. Through a literature search of studies published from 1980 to 2017, we found that children with LCH showed a generally favorable recovery from neurological dysfunction after the acute phase of spinal symptoms.

CONCLUSION

This report underscores the utility of emergency radiotherapy for the neurological recovery of spinal LCH in infants. Our long-term observation further denotes the value of this treatment in terms of the intact survival with preserved motor functions and physical growth.

摘要

背景

朗格汉斯细胞组织细胞增多症(LCH)是一种克隆性疾病,具有局灶性或播散性病变,可压迫周围组织,包括脊髓。由于很少有报道将脊柱症状描述为儿童LCH的首发表现,其长期神经学预后仍不明确。

病例报告及文献综述

我们报告一名21个月大的男孩,他突然出现截瘫。影像学分析显示,溶骨性病变和硬膜外肿瘤压迫T7 - 9椎体水平的脊髓。在他出现腿部无力12天后,在肿瘤活检后开始了紧急放疗。在放疗过程中,瘫痪症状逐渐改善。在排除感染并确定LCH的病理诊断后,开始了多药化疗。在总共15 Gy的放疗及后续化疗后,他的完全性截瘫明显改善,4岁时未遗留神经后遗症。通过检索1980年至2017年发表的研究文献,我们发现LCH患儿在脊柱症状急性期后神经功能障碍通常恢复良好。

结论

本报告强调了紧急放疗对婴儿脊柱LCH神经功能恢复的作用。我们的长期观察进一步表明了这种治疗在保留运动功能和身体生长的完整生存方面的价值。

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