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神经影像学与原发性中枢神经系统淋巴瘤肿块样脱髓鞘病变和首发灶之间的临床病理差异。

Neuroimaging and clinicopathological differences between tumefactive demyelinating lesions and sentinel lesions of primary central nervous system lymphoma.

机构信息

Senior Department of Neurology, The First Medical Center of PLA General Hospital, Beijing, China.

Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.

出版信息

Front Immunol. 2022 Aug 18;13:986473. doi: 10.3389/fimmu.2022.986473. eCollection 2022.

DOI:10.3389/fimmu.2022.986473
PMID:36059526
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9433969/
Abstract

OBJECTIVE

It is still a challenge to distinguish sentinel lesions of primary central nervous system lymphoma (PCNSL) from atypical tumefactive demyelinating lesions (TDLs) in clinical practice. We aimed to investigate potential differences of clinical features, neuroimaging findings and pathological characteristics between PCNSL and TDLs, improving early accurate diagnosis.

METHODS

It was a retrospective study involving 116 patients with TDLs and 150 patients with PCNSLs. All cases were pathologically confirmed. Clinical features, neuroimaging findings and pathological characteristics between two groups were analyzed.

RESULTS

The onset age was 37 ± 14 years in TDLs and 58 ± 13 years in PCNSL(p=0.000). Main onset symptom was headache in TDLs, while cognitive impairment was frequently noted in PCNSL. CT brain scan image showed hypodense lesions in most cases of TDL (110/116, 94.8%), while approximately 80% patients (120/150) with PCNSL had hyperdense lesions. Furthermore, we found that the presence of Creutzfeldt-Peters cells (might be misdiagnosed as tumor cells) may serve as an important feature in TDLs.

CONCLUSIONS

Onset age of patients with TDLs was younger than PCNSL. Neuroimaging features on brain CT scan might provide clues to make a differential diagnosis. Pathological features of PCNSL with sentinel lesions or following steroids therapy might mimic TDLs. Dynamic neuroimaging pathological and follow-up information were essential for an accurate diagnosis.

摘要

目的

在临床实践中,区分原发性中枢神经系统淋巴瘤(PCNSL)的哨兵病变与非典型肿块性脱髓鞘病变(TDL)仍然具有挑战性。我们旨在研究 PCNSL 和 TDL 之间在临床特征、神经影像学表现和病理特征方面的潜在差异,以提高早期准确诊断。

方法

这是一项回顾性研究,共纳入 116 例 TDL 患者和 150 例 PCNSL 患者。所有病例均经病理证实。分析两组之间的临床特征、神经影像学表现和病理特征。

结果

TDL 的发病年龄为 37±14 岁,PCNSL 为 58±13 岁(p=0.000)。TDL 的主要首发症状为头痛,而 PCNSL 则常表现为认知障碍。CT 脑扫描图像显示 TDL 大多数病例为低信号病变(110/116,94.8%),而约 80%的 PCNSL 患者(120/150)有高信号病变。此外,我们发现 Creutzfeldt-Peters 细胞的存在(可能误诊为肿瘤细胞)可能是 TDL 的一个重要特征。

结论

TDL 患者的发病年龄小于 PCNSL。脑 CT 扫描的神经影像学特征可能为鉴别诊断提供线索。PCNSL 伴哨兵病变或激素治疗后的病理特征可能类似于 TDL。动态神经影像学、病理和随访信息对准确诊断至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a1c/9433969/da2862cff264/fimmu-13-986473-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a1c/9433969/a8cbf02fabe8/fimmu-13-986473-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a1c/9433969/018ba5a79957/fimmu-13-986473-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a1c/9433969/4b13ab092e61/fimmu-13-986473-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a1c/9433969/6e23b5202055/fimmu-13-986473-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a1c/9433969/da2862cff264/fimmu-13-986473-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a1c/9433969/a8cbf02fabe8/fimmu-13-986473-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a1c/9433969/018ba5a79957/fimmu-13-986473-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a1c/9433969/4b13ab092e61/fimmu-13-986473-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a1c/9433969/6e23b5202055/fimmu-13-986473-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a1c/9433969/da2862cff264/fimmu-13-986473-g005.jpg

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