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脊柱淋巴瘤样肉芽肿病例的系统评价

Systematic Review of Spinal Lymphomatoid Granulomatosis Cases.

作者信息

Iwamoto Naotaka, Kim Kyongsong, Kokubo Rinko, Isu Toyohiko, Morimoto Daijiro, Omura Tomoko, Saito Koji, Kikuchi Yoshinao, Ota Yasunori, Matsuno Akira, Morita Akio

机构信息

Department of Neurosurgery, Nippon Medical School Hospital, Tokyo, Japan.

Department of Neurosurgery, Teikyo University School of Medicine, Tokyo, Japan.

出版信息

World Neurosurg X. 2021 Apr 30;11:100106. doi: 10.1016/j.wnsx.2021.100106. eCollection 2021 Jul.

Abstract

Lymphomatoid granulomatosis (LYG) is a rare Epstein-Barr virus-associated systemic angiocentric and angiodestructive lymphoproliferative disorder. It commonly involves the lungs and can also affect the skin, liver, kidney, and central nervous system. It can rarely occur in the spine, however, the details are unclear. We performed a systematic review of published cases (including our 1 case) of spinal LYG. We performed a systematic search of studies in English on spinal LYG, focusing on its clinical features, imaging, and treatments, according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines on the PubMed database. We identified 14 patients from the literature. We also found 1 case of isolated cervical LYG (grade 3) who was treated with steroid and radiation therapy for the spinal lesion after pathologic diagnosis. We performed a pooled analysis of these 15 cases. The mean age was 43.4 years, and 13 of the 15 patients were male. Brain lesions were present in 11 of 12 intramedullary spinal lesions, and only 1 was an isolated spinal LYG case. Regarding the diagnostic methods, 1 case was not described. Of the 14 cases described, 12 patients underwent biopsies (7 brain, 4 lung, and 1 spinal cord lesion) and 2 underwent surgical removal for an extramedullary lesion. In the overall prognosis from a mean follow-up period of 21.6 months, 4 patients died despite several treatments. Spinal LYG, particularly isolated spinal LYG, is rare. Thus further accumulation of cases may be necessary to better understand its characteristics.

摘要

淋巴瘤样肉芽肿病(LYG)是一种罕见的与爱泼斯坦-巴尔病毒相关的系统性血管中心性和血管破坏性淋巴增殖性疾病。它通常累及肺部,也可影响皮肤、肝脏、肾脏和中枢神经系统。然而,它很少发生在脊柱,具体情况尚不清楚。我们对已发表的脊柱LYG病例(包括我们的1例病例)进行了系统综述。根据PubMed数据库上系统评价和Meta分析的首选报告项目指南,我们对英文文献中关于脊柱LYG的研究进行了系统检索,重点关注其临床特征、影像学表现和治疗方法。我们从文献中确定了14例患者。我们还发现1例孤立性颈椎LYG(3级)患者,在病理诊断后接受了类固醇和放射治疗以治疗脊柱病变。我们对这15例病例进行了汇总分析。平均年龄为43.4岁,15例患者中有13例为男性。12例脊髓内病变中有11例存在脑部病变,只有1例是孤立性脊柱LYG病例。关于诊断方法,有1例未作描述。在描述的14例病例中,12例患者接受了活检(7例脑部、4例肺部和1例脊髓病变),2例因髓外病变接受了手术切除。在平均21.6个月的随访期的总体预后中,尽管进行了多种治疗,仍有4例患者死亡。脊柱LYG,尤其是孤立性脊柱LYG,很罕见。因此,可能需要进一步积累病例以更好地了解其特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b326/8181181/b16b1919beb7/gr1.jpg

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