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颅内原发性结外Rosai-Dorfman病的影像学诊断特征:两例报告及文献复习

Imaging diagnostic features of intracranial primary extranodal Rosai-Dorfman disease: Two case reports and literature review.

作者信息

Cao Gan, Xie Shanghuang, Li Mifang, Yang Xiaolin, Zhu Jichao, Zhang Lingyan

机构信息

Department of Medical Imaging, Longgang Central Hospital of Shenzhen, 6082 Longgang Avenue, Longgang District, Shenzhen, 518000, China.

出版信息

Radiol Case Rep. 2023 Apr 7;18(6):2165-2171. doi: 10.1016/j.radcr.2023.03.007. eCollection 2023 Jun.

DOI:10.1016/j.radcr.2023.03.007
PMID:37089978
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10120362/
Abstract

In this report, we describe 2 cases of rare intracranial extranodal Rosai-Dorfman disease. The occurrence of this type of non-Langerhans cell histiocytosis in the central nervous system is infrequent, with less than 5% of cases. The first patient was a 35-year-old male who presented with recurring headaches, and the second patient was a 50-year-old male who reported sudden onset of dizziness and vomiting. Computed tomography scans were performed in both cases, but magnetic resonance imaging played a crucial role in the characterization of the lesions and their locations in the thalamus, third ventricle, lateral ventricles, and cerebellopontine angle area. The final diagnosis was confirmed through pathological examination and immunohistochemistry following brain tumor resection. These cases underscore the significance of magnetic resonance imaging in the early diagnosis of intracranial extranodal Rosai-Dorfman disease.

摘要

在本报告中,我们描述了2例罕见的颅内结外Rosai-Dorfman病。这种类型的非朗格汉斯细胞组织细胞增生症在中枢神经系统中并不常见,病例占比不到5%。首例患者为一名35岁男性,表现为反复头痛,第二例患者为一名50岁男性,报告突然出现头晕和呕吐。两例患者均进行了计算机断层扫描,但磁共振成像在病变特征及其在丘脑、第三脑室、侧脑室和桥小脑角区域的定位方面发挥了关键作用。脑肿瘤切除术后通过病理检查和免疫组织化学确诊。这些病例强调了磁共振成像在颅内结外Rosai-Dorfman病早期诊断中的重要性。

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本文引用的文献

1
MR imaging of cerebral involvement of Rosai-Dorfman disease: a single-centre experience with review of the literature.磁共振成像在罗道氏病脑内侵犯中的应用:单中心经验并文献复习
Radiol Med. 2021 Jan;126(1):89-98. doi: 10.1007/s11547-020-01226-7. Epub 2020 May 26.
2
Disease Characteristics, Radiologic Patterns, Comorbid Diseases, and Ethnic Differences in 32 Patients With Rosai-Dorfman Disease.32例Rosai-Dorfman病患者的疾病特征、影像学表现、合并疾病及种族差异
J Comput Assist Tomogr. 2020 May/Jun;44(3):450-461. doi: 10.1097/RCT.0000000000000983.
3
Isolated Intraventricular Rosai-Dorfman Disease.孤立性脑室内Rosai-Dorfman病
Asian J Neurosurg. 2018 Oct-Dec;13(4):1285-1287. doi: 10.4103/ajns.AJNS_134_18.
4
Consensus recommendations for the diagnosis and clinical management of Rosai-Dorfman-Destombes disease.罗萨-多夫曼-德斯东贝病的诊断和临床管理共识建议。
Blood. 2018 Jun 28;131(26):2877-2890. doi: 10.1182/blood-2018-03-839753. Epub 2018 May 2.
5
Cranio-spinal Rosai Dorfman disease: case series and literature review.颅-脊髓型罗萨伊-多夫曼病:病例系列及文献综述
Br J Neurosurg. 2019 Apr;33(2):176-183. doi: 10.1080/02688697.2017.1329517. Epub 2017 May 22.
6
Imaging characteristics of Rosai-Dorfman disease in the central nervous system.中枢神经系统 Rosai-Dorfman 病的影像学特征。
Eur J Radiol. 2012 Jun;81(6):1265-72. doi: 10.1016/j.ejrad.2011.03.006. Epub 2011 Mar 25.
7
May 2002: 38-year-old man and 69-year-old woman with dural based masses.2002年5月:患有硬膜下肿块的38岁男性和69岁女性。
Brain Pathol. 2002 Oct;12(4):517-8, 521. doi: 10.1111/j.1750-3639.2002.tb00471.x.
8
The neurologic manifestations of sinus histiocytosis with massive lymphadenopathy.伴有巨大淋巴结病的窦性组织细胞增多症的神经学表现。
Neurology. 1982 Apr;32(4):365-72. doi: 10.1212/wnl.32.4.365.
9
[Adenitis with lipid excess, in children or young adults, seen in the Antilles and in Mali. (4 cases)].[脂质过多性腺炎,见于安的列斯群岛和马里的儿童或年轻人。(4例)]
Bull Soc Pathol Exot Filiales. 1965 Nov-Dec;58(6):1169-75.
10
Sinus histiocytosis with massive lymphadenopathy. A newly recognized benign clinicopathological entity.伴有巨大淋巴结病的窦性组织细胞增多症。一种新认识的良性临床病理实体。
Arch Pathol. 1969 Jan;87(1):63-70.