刘昊雨, 宋周扬, 潘登, 周惠, 钟方云, 于丽娟. 多系统朗格汉斯细胞组织细胞增生症 18F-FDG PET/CT 显像1例[J]. 国际放射医学核医学杂志. DOI: 10.3760/cma.j.cn121381-202309017-00393
引用本文: 刘昊雨, 宋周扬, 潘登, 周惠, 钟方云, 于丽娟. 多系统朗格汉斯细胞组织细胞增生症 18F-FDG PET/CT 显像1例[J]. 国际放射医学核医学杂志. DOI: 10.3760/cma.j.cn121381-202309017-00393
Haoyu Liu, Zhouyang Song, Deng Pan, Hui Zhou, Fangyun Zhong, Lijuan Yu. Multi-system Langerhans cell histiocytosis in 18F-FDG PET/CT imaging: a case report[J]. Int J Radiat Med Nucl Med. DOI: 10.3760/cma.j.cn121381-202309017-00393
Citation: Haoyu Liu, Zhouyang Song, Deng Pan, Hui Zhou, Fangyun Zhong, Lijuan Yu. Multi-system Langerhans cell histiocytosis in 18F-FDG PET/CT imaging: a case report[J]. Int J Radiat Med Nucl Med. DOI: 10.3760/cma.j.cn121381-202309017-00393

多系统朗格汉斯细胞组织细胞增生症 18F-FDG PET/CT 显像1例

Multi-system Langerhans cell histiocytosis in 18F-FDG PET/CT imaging: a case report

  • 摘要: 朗格汉斯细胞组织细胞增生症(LCH)是一种罕见的未成熟树突状细胞异常增生的肿瘤性疾病,其组织病理学检查为诊断的“金标准”。笔者报道了1例青少年多系统LCH的CT、MRI及18F-氟脱氧葡萄糖(FDG) PET/CT显像病例,从临床、组织病理学、影像、治疗等方面分析了该病的特点,并通过文献复习加深了对该病的认识,为该病的诊断提供更多参考。

     

    Abstract: Langerhans cell histiocytosis (LCH) is a rare neoplastic disease with abnormal proliferation of immature dendritic cells, and histopathological examination is the "gold standard" for its diagnosis. The author reports a case of multisystem LCH in an adolescent with CT, MRI, and 18F-fluorodeoxyglucose(FDG) PET/CT imaging, and analyzes the characteristics of the disease from the clinical, histopathological, imaging, and therapeutic perspectives, and deepens the understanding of the disease by reviewing the literature to provide more references for the diagnosis of the disease.

     

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