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非霍奇金淋巴瘤患者的渗透性脱髓鞘综合征:病例报告及文献复习。

Osmotic demyelination syndrome in patients with non-Hodgkin lymphoma: a case report and literature review.

机构信息

Department of Neurology and Psychiatry, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, México City, México.

Department of Neurology, Hospital Civil de Guadalajara Fray Antonio Alcalde, Guadalajara, Jalisco, México.

出版信息

Int J Neurosci. 2023 Mar;133(3):233-237. doi: 10.1080/00207454.2021.1909009. Epub 2021 Sep 24.

Abstract

INTRODUCTION

Osmotic demyelination syndrome (ODS) is a non-inflammatory process of the central nervous system caused by extracellular osmotic changes, which leads to oligodendrocyte apoptosis and disruption of myelin sheaths, usually affecting patients with underlying systemic conditions that impose susceptibility to osmotic stress. Description of ODS in patients with non-Hodgkin lymphoma (NHL) is limited to a few case reports.

METHODS

Here, we report a 44-year-old man with NHL that had an incidental diagnosis of ODS. We conducted a literature review of the published cases of ODS in NHL patients from 1959 to 2020, aiming to describe the characteristics of these patients.

RESULTS

A total of seven patients were summarized (four men and three women), including our case and six patients from published reports. Risk factors such as weight loss and alcoholism were reported in five (71.4%) patients. Hyponatremia was found in six (85.7%) of the cases, and none of them had overly rapid sodium correction. Four cases were asymptomatic, and diffuse large B-cell lymphoma was the most common subtype of NHL (85.7%). The outcome was favorable in most cases; only two deaths not directly related to ODS were reported.

CONCLUSION

We wish to suggest that systemic and metabolic stress induced by NHL may be associated with the development of central osmotic demyelination, and therefore, NHL may be a novel risk factor for ODS. Clinicians should be aware of ODS in patients with hematological malignancies, even in the absence of traditional risk factors.

摘要

简介

渗透性脱髓鞘综合征(ODS)是一种由细胞外渗透压变化引起的中枢神经系统非炎症性过程,导致少突胶质细胞凋亡和髓鞘鞘破坏,通常影响具有对渗透压应激敏感的潜在系统性疾病的患者。非霍奇金淋巴瘤(NHL)患者的 ODS 描述仅限于少数病例报告。

方法

在这里,我们报告了一例 44 岁患有 NHL 的男性患者,其偶然诊断为 ODS。我们对 1959 年至 2020 年发表的 NHL 患者 ODS 病例进行了文献回顾,旨在描述这些患者的特征。

结果

共总结了 7 例患者(4 名男性和 3 名女性),包括我们的病例和 6 名来自已发表报告的患者。5 例(71.4%)患者报告有体重减轻和酗酒等危险因素。6 例(85.7%)存在低钠血症,且均未过度快速纠正钠。4 例无症状,弥漫性大 B 细胞淋巴瘤是 NHL 最常见的亚型(85.7%)。大多数情况下结局良好;仅报告了 2 例与 ODS 无关的死亡。

结论

我们建议 NHL 引起的全身和代谢应激可能与中枢性渗透压脱髓鞘的发展有关,因此 NHL 可能是 ODS 的一个新的危险因素。临床医生应意识到血液系统恶性肿瘤患者存在 ODS,即使没有传统的危险因素。

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