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原发性颅内淋巴瘤

Primary intracranial lymphomas.

作者信息

Mufti Shagufta T, Baeesa Saleh S, Al-Maghrabi Jaudah A

机构信息

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

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

出版信息

Asian J Neurosurg. 2016 Jul-Sep;11(3):232-9. doi: 10.4103/1793-5482.145082.

Abstract

BACKGROUND

Primary CNS lymphoma (PCNSL), a rare form of aggressive extranodal non-Hodgkin's lymphoma (NHL), has increased in incidence during the last three decades and occurs in both immune compromised and immune competent hosts. It has an overall poor prognosis.

OBJECTIVE

This study attempts to further delineate the clinico-pathological, immunohistochemical and radiological profile of PCNSL at Jeddah to King Faisal Hospital and Research Center.

METHODS

Computerized search through the archives of King Faisal Hospital and Research Centre between July 2000- December 2012 identified 15 patients with pathologically confirmed PCNSL. These were analyzed retrospectively. Their clinico-pathological, immunohistochemical and radiological data were analyzed.

RESULTS

Of the 15 PCNSL patients, 8 (53.3%) were females and 7 (46.6%) were males. There was female predilection especially in the age group of 40-59 years. Mean age at diagnosis for all patients was 50.4 years. There was no patient in the pediatric age group. The most common location in the brain was the frontal region in 7 patients (46.6%), 7 (46.6%) had multiple intracranial masses; all 15 (100%) were Non Hodgkin B-cell lymphomas, among which 13 (86.6%) were diffuse large B-cell lymphomas. All 15 (100%) cases showed diffuse and strong positivity for CD 45, and CD 20. Fourteen patients were immune competent while one was immune compromised.

CONCLUSIONS

PCNSL often occurs in middle-aged and aged patients. There is female predilection especially in the middle age. Frontal region is the most common location with diffuse large B-cell lymphoma being the predominant subtype.

摘要

背景

原发性中枢神经系统淋巴瘤(PCNSL)是侵袭性结外非霍奇金淋巴瘤(NHL)的一种罕见形式,在过去三十年中发病率有所上升,可发生于免疫功能低下和免疫功能正常的宿主。其总体预后较差。

目的

本研究旨在进一步描述吉达法赫德国王医院及研究中心PCNSL的临床病理、免疫组化和放射学特征。

方法

通过计算机检索法赫德国王医院及研究中心2000年7月至2012年12月的档案,确定15例经病理证实的PCNSL患者。对这些患者进行回顾性分析。分析他们的临床病理、免疫组化和放射学数据。

结果

15例PCNSL患者中,8例(53.3%)为女性,7例(46.6%)为男性。女性更易患病,尤其是在40 - 59岁年龄组。所有患者的平均诊断年龄为50.4岁。儿科年龄组无患者。脑内最常见的部位是额叶,有7例(46.6%);7例(46.6%)有多个颅内肿块;所有15例(100%)均为非霍奇金B细胞淋巴瘤,其中13例(86.6%)为弥漫性大B细胞淋巴瘤。所有15例(100%)病例CD45和CD20均呈弥漫性强阳性。14例患者免疫功能正常,1例免疫功能低下。

结论

PCNSL常发生于中老年患者。女性更易患病,尤其是中年女性。额叶是最常见的部位,弥漫性大B细胞淋巴瘤是主要亚型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b089/4849292/17affbed6103/AJNS-11-232-g001.jpg

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