Suppr超能文献

原发性中枢神经系统伯基特淋巴瘤,以长期波动的意识水平为表现:一例病例报告及诊断与管理挑战相关文献复习。

Primary Central Nervous System Burkitt Lymphoma, Presenting with Long-Term Fluctuating Level of Consciousness: A Case Report and Literature Review on Challenges in Diagnosis and Management.

机构信息

Department of Hematology, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.

Hematology Research Unit, King Fahd Medical Research Center, King Abdulaziz University, Jeddah, Saudi Arabia.

出版信息

Am J Case Rep. 2022 Jun 21;23:e936401. doi: 10.12659/AJCR.936401.

Abstract

BACKGROUND Burkitt lymphoma (BL) is an aggressive subtype of B-cell non-Hodgkin lymphoma (NHL) rarely affecting the central nervous system (CNS) as a primary disease. Over the past years, only a few cases of primary CNS Burkitt lymphoma were reported. There is a challenge in early recognition and diagnosis of this type of brain lymphoma. Furthermore, there is no specific treatment protocols for primary CNS Burkitt lymphoma, which adds to the difficulty in managing those patients. We introduce a case of a 65-year-old who presented with fluctuating memory disturbance diagnosed as cerebral Burkitt lymphoma. CASE REPORT A 65-year-old man developed a gradual decrease in his level of consciousness over a span of 4 days, associated with fluctuating memory disturbances. A CT scan showed a hyperdense mass in the region of the trigon of the left lateral ventricle and marked obstructive hydrocephalus involving the temporal, occipital horns, and the left lateral ventricle, with no evidence of other suspicious lesions. A brain biopsy of the lesion revealed features of encephalitis initially, but the patient presented later with worsening symptoms, and a repeated brain biopsy showed features of Burkett lymphoma, with normal pan-CT scan. CONCLUSIONS Primary CNS Burkitt lymphoma (PCNSBL) is a rare disease with no clear evidence in the literature of how to deal with it. Reporting such cases provides a better understanding of how to approach such unusual presentations. Treatment of PCNSBL is challenging and even with the currently adopted approaches, the disease still has a very poor outcome.

摘要

背景

伯基特淋巴瘤(BL)是一种侵袭性 B 细胞非霍奇金淋巴瘤(NHL)亚型,很少作为原发性疾病影响中枢神经系统(CNS)。在过去的几年中,仅报道了少数几例原发性中枢神经系统伯基特淋巴瘤病例。这种类型的脑淋巴瘤在早期识别和诊断方面存在挑战。此外,针对原发性中枢神经系统伯基特淋巴瘤尚无特定的治疗方案,这增加了管理这些患者的难度。我们介绍了一例 65 岁男性患者,表现为波动记忆障碍,诊断为脑伯基特淋巴瘤。

病例报告

一名 65 岁男性,在 4 天的时间里逐渐出现意识水平下降,伴有波动的记忆障碍。CT 扫描显示左侧侧脑室三角区高密度肿块,伴有明显的阻塞性脑积水,累及颞叶、枕叶角和左侧侧脑室,但无其他可疑病变的证据。病变的脑活检最初显示脑炎的特征,但患者随后出现症状恶化,重复的脑活检显示伯基特淋巴瘤的特征,全脑 CT 扫描正常。

结论

原发性中枢神经系统伯基特淋巴瘤(PCNSBL)是一种罕见疾病,文献中尚无明确证据表明如何治疗。报告此类病例有助于更好地了解如何处理此类不常见的表现。PCNSBL 的治疗具有挑战性,即使采用目前采用的方法,疾病的预后仍然非常差。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7131/9235913/38433c789a6a/amjcaserep-23-e936401-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验