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[核医学在 Erdheim-Chester 病中的应用:里尔的经验]

[Usefulness of nuclear medicine in Erdheim-Chester disease: A Lille experience].

作者信息

Adens A, Landy P, Terriou L, Baillet C, Beron A, Lambert M, Launay D, Huglo D

机构信息

Service de médecine nucléaire, hôpital Claude-Huriez, CHRU de Lille, rue Michel-Polonowski, 59000 Lille, France; Département de biophysique, faculté de médecine Henri-Warembourg, université de Lille 2, 59120 Loos, France.

Service de médecine interne, hôpital Claude-Huriez, CHRU de Lille, rue Michel-Polonowski, 59000 Lille, France.

出版信息

Rev Med Interne. 2017 Apr;38(4):235-242. doi: 10.1016/j.revmed.2016.10.386. Epub 2017 Mar 3.

Abstract

INTRODUCTION

Erdheim-Chester disease is a rare form of non-langerhans histiocytosis and its etiology is still not well established. The aims of the study were to assess the value of the bone scintigraphy and the F-FDG PET/CT for the diagnostic and for the latter in the therapeutic evaluation.

METHODS

We retrospectively reviewed 49 patients suspected of Erdheim-Chester disease between 2004 and 2016. Bone scintigraphy was compared with histopathology and PET-CT to conventional morphological examinations and bone scintigraphy. For therapeutic evaluation, thresholds similar to PERCIST 1.0 were used.

RESULTS

Forty-nine bone scintigraphy were evaluated with a sensitivity of 100%, a specificity 97%, a positive predictive value 90% and a negative predictive value of 100%. Eight patients had at least an initial PET-CT. The sensitivity compared to conventional morphological examinations differed from the location but was excellent for orbital, bone and vascular involvements. Specificity was comparable between the different examinations. Six patients treated with interferon and three with vemurafenib were followed by PET-CT. PET-CT, in agreement to clinicobiological data, identified 4 partial responses and one complete response with interferon et two partial responses and one complete response with vemurafenib.

CONCLUSION

Our retrospective study suggests that bone scintigraphy and 18F-FDG PET/CT could be useful in the initial assessment of Erdheim-Chester disease but also for the latter in the therapeutic evaluation.

摘要

引言

厄尔德海姆-切斯特病是一种罕见的非朗格汉斯组织细胞增多症,其病因仍未完全明确。本研究的目的是评估骨闪烁显像和F-FDG PET/CT在诊断方面的价值,以及后者在治疗评估中的价值。

方法

我们回顾性分析了2004年至2016年间49例疑似厄尔德海姆-切斯特病的患者。将骨闪烁显像与组织病理学以及PET-CT与传统形态学检查和骨闪烁显像进行比较。在治疗评估中,采用了与PERCIST 1.0相似的阈值。

结果

对49例骨闪烁显像进行了评估,其灵敏度为100%,特异性为97%,阳性预测值为90%,阴性预测值为100%。8例患者至少进行了一次初始PET-CT检查。与传统形态学检查相比,其灵敏度因病变部位而异,但对眼眶、骨骼和血管受累情况的诊断效果极佳。不同检查之间的特异性相当。6例接受干扰素治疗和3例接受维莫非尼治疗的患者接受了PET-CT随访。PET-CT与临床生物学数据一致,确定干扰素治疗有4例部分缓解和1例完全缓解,维莫非尼治疗有2例部分缓解和1例完全缓解。

结论

我们的回顾性研究表明,骨闪烁显像和18F-FDG PET/CT不仅在厄尔德海姆-切斯特病的初始评估中可能有用,而且在治疗评估中也可能有用。

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