Department of Radiology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts, USA.
Pediatr Blood Cancer. 2023 Jan;70(1):e30057. doi: 10.1002/pbc.30057. Epub 2022 Oct 20.
Currently, there is no consensus protocol on the initial staging evaluation for Langerhans cell histiocytosis (LCH). Our institutional protocol consists of a skeletal survey and a whole-body positron emission tomography with 2-deoxy-2-[fluorine-18] fluoro-D-glucose integrated with computed tomography (FDG PET/CT) study. The utility of the PET/CT lies in its sensitivity in detecting osseous and extra-osseous lesions, and in determining the baseline metabolic activity of LCH lesions to assess treatment response. However, the added utility of the skeletal survey in staging LCH is unclear. Therefore, this study retrospectively assessed the added diagnostic value of skeletal surveys in patients with baseline PET/CTs for initial staging of LCH.
We retrospectively searched the medical records of all patients less than or equal to 18 years old at a large children's hospital (May 2013 to September 2021). The inclusion criteria were (a) biopsy-proven diagnosis of LCH and (b) initial staging PET/CT and skeletal survey performed less than or equal to 1 month apart. A blinded pediatric radiologist reviewed the skeletal surveys and another reviewed the PET/CTs in identifying LCH osseous lesions.
Our study cohort consisted of 49 children with 86 LCH osseous lesions. In non-extremity locations, PET/CT identified 70/70 (100%) osseous lesions, while skeletal surveys detected 43/70 (61.4%) osseous lesions. In the extremities, PET/CT identified 13/16 (81.3%) osseous lesions, while skeletal surveys detected 15/16 (93.8%) osseous lesions.
Skeletal surveys increased the detection rate of osseous lesions in the extremities, but added no diagnostic value to the detection of osseous lesions in non-extremity locations. Therefore, we propose to abbreviate the skeletal survey to include only extremity radiographs.
目前,朗格汉斯细胞组织细胞增生症(LCH)的初始分期评估尚无共识方案。我们的机构方案包括骨骼检查和全身正电子发射断层扫描与 2-脱氧-2-[氟-18]氟代-D-葡萄糖结合计算机断层扫描(FDG PET/CT)研究。PET/CT 的作用在于其在检测骨内和骨外病变方面的敏感性,以及确定 LCH 病变的基线代谢活性以评估治疗反应。然而,骨骼检查在分期 LCH 中的额外作用尚不清楚。因此,本研究回顾性评估了基线 PET/CT 分期时骨骼检查对 LCH 初始分期的附加诊断价值。
我们回顾性搜索了一家大型儿童医院(2013 年 5 月至 2021 年 9 月)所有小于或等于 18 岁的患者的病历。纳入标准为:(a)经活检证实的 LCH 诊断和(b)在 PET/CT 初始分期后 1 个月内进行骨骼检查。一名盲法儿科放射科医生回顾了骨骼检查,另一名医生回顾了 PET/CT 以识别 LCH 骨病变。
我们的研究队列包括 49 名儿童,共 86 个 LCH 骨病变。在非四肢部位,PET/CT 发现了 70/70(100%)个骨病变,而骨骼检查发现了 43/70(61.4%)个骨病变。在四肢部位,PET/CT 发现了 13/16(81.3%)个骨病变,而骨骼检查发现了 15/16(93.8%)个骨病变。
骨骼检查提高了四肢骨病变的检出率,但对非四肢骨病变的检出无诊断价值。因此,我们建议将骨骼检查缩写为仅包括四肢 X 线摄影。