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起源于侧脑室的原发性颅内黏膜相关淋巴组织边缘区B细胞淋巴瘤:病例报告及发病机制综述

Primary intracranial marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue arising in the lateral ventricle: Case report and review of pathogenesis.

作者信息

Hajtovic Sabastian, Yu Edward, Bershadskiy Alexander, Sacho Raphael, Gilad Ronit

机构信息

Department of Neurosurgery, Staten Island University Hospital, Staten Island, New York, United States.

Department of Neurology, Staten Island University Hospital, Staten Island, New York, United States.

出版信息

Surg Neurol Int. 2022 Apr 29;13:181. doi: 10.25259/SNI_54_2022. eCollection 2022.

Abstract

BACKGROUND

Primary central nervous system lymphoma (PCNSL) is an aggressive extranodal subtype of nonHodgkin's lymphoma. Ventricle-predominant PCNSL, arising in the CNS ventricular system, is a rare entity. In over 90% of cases, PCNSL is classified as diffuse large B-cell lymphoma. Rarely, PCNSL may be classified as marginal zone B-cell lymphoma (MZBCL) of mucosa-associated lymphoid tissue (MALT). Taken together, a primary MALT-type MZBCL arising in a cerebral ventricle is an extremely rare presentation.

CASE DESCRIPTION

A 69-year-old female presented with a persistent left frontal headache for 1 year. Magnetic resonance imaging revealed an enhancing soft-tissue lesion within the left lateral ventricle, with associated periventricular edema. We performed an excisional biopsy of the tumor, which grossly had the appearance of a meningioma. Histopathology of the tumor was consistent with MZBCL of the MALT type. The patient was treated with Rituximab and Ibrutinib. Six months after surgery, she remained neurologically intact and free of disease.

CONCLUSION

We report the case of a primary MALT-type MZBCL arising in the CNS ventricular system, with characteristics mimicking meningioma. This lymphoma involved the lateral ventricle and likely originated from the choroid plexus. Meningothelial cells and epithelial cells in the choroid plexus may acquire MALT in response to chronic inflammatory stimuli, such as infection or autoimmune disease. In rare cases, MALT lymphoma may develop as part of this pathogenesis.

摘要

背景

原发性中枢神经系统淋巴瘤(PCNSL)是一种侵袭性的非霍奇金淋巴瘤结外亚型。以脑室为主的PCNSL起源于中枢神经系统脑室系统,是一种罕见的实体。在超过90%的病例中,PCNSL被归类为弥漫性大B细胞淋巴瘤。很少情况下,PCNSL可能被归类为黏膜相关淋巴组织(MALT)的边缘区B细胞淋巴瘤(MZBCL)。总体而言,起源于脑室的原发性MALT型MZBCL是一种极其罕见的表现。

病例描述

一名69岁女性因持续性左额叶头痛1年就诊。磁共振成像显示左侧脑室内有一个强化的软组织病变,并伴有脑室周围水肿。我们对肿瘤进行了切除活检,大体外观类似脑膜瘤。肿瘤的组织病理学与MALT型MZBCL一致。患者接受了利妥昔单抗和伊布替尼治疗。手术后6个月,她神经系统功能完好,无疾病迹象。

结论

我们报告了一例起源于中枢神经系统脑室系统的原发性MALT型MZBCL病例,其特征类似脑膜瘤。这种淋巴瘤累及侧脑室,可能起源于脉络丛。脉络丛中的脑膜上皮细胞和上皮细胞可能因慢性炎症刺激(如感染或自身免疫性疾病)而获得MALT。在罕见情况下,MALT淋巴瘤可能作为这种发病机制的一部分而发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41ca/9062969/1c32827d785b/SNI-13-181-g001.jpg

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