Palavani Lucca B, Bapat Atharva, Batista Sávio, Mendes João Pedro, Oliveira Leonardo B, Bertani Raphael
Department of Medicine, Max Planck University Center, São Paulo, Brazil.
Trivandrum Medical College, Thiruvananthapuram, Kerala, India.
Asian J Neurosurg. 2024 Jun 6;19(2):137-144. doi: 10.1055/s-0044-1787535. eCollection 2024 Jun.
Extramedullary plasmacytoma (EMP) is an uncommon disorder characterized by the development of abnormal plasma cell tumors outside the bone marrow. These tumors are typically observed in various locations, including the upper respiratory tract, gastrointestinal tract, and other soft tissues. Among the less explored manifestations of EMP is intracranial EMP, which remains poorly understood due to the limited literature available on the subject. The objective was to comprehend the population characteristics, localization, type, treatment, and outcomes of intracranial EMP. A systematic review of the literature for EMPs was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analysis guidelines. The strategy "extramedullary plasmacytoma AND multiple myeloma" was used for the search. The search terms were queried using PubMed, Embase, Scopus, Cochrane, and Web of Science databases. We included only those studies that presented clinical studies with patients diagnosed with intracranial plasmacytomas. In this study, a total of 84 patients from 25 studies were analyzed. The average age of diagnosis was 57.25 years, with a slightly higher proportion of females (57%) compared to male patients (43%). The most common locations of intracranial plasmacytomas were the clivus (29.7%), frontal lobe (18.9%), parietal lobe (8.1%), occipital lobe (6.7%), temporal lobe (6.7%), and sphenoid (4%). Chordoma and meningioma were the most common differential diagnoses encountered during clinical investigations. Treatment modalities included radiotherapy (RT), chemotherapy (QT), surgical resection (SR), and conservative approaches. The most frequent treatment combinations were SR + RT (19%) and RT only (17.8%). Mortality was reported in 48% of the cases, with complete resolution observed in 10 cases and partial resolution in 3 cases. The average follow-up duration was 37.5 months. The clivus is the most frequently reported site of extramedullary intracranial plasmacytoma (EMIP) occurrence, representing 29.7% of cases. Chordomas were commonly observed alongside EMIPs and emerged as the primary differential diagnosis. RT was the predominant treatment modality, with SR considered when feasible. RT alone demonstrated the highest effectiveness in managing EMIPs (30%), while QT as a sole intervention showed lower efficacy. However, a combination of dexamethasone, lenalidomide, and targeted RT displayed promising results, offering improved tumor response and increased safety.
髓外浆细胞瘤(EMP)是一种罕见的疾病,其特征是在骨髓外出现异常浆细胞瘤。这些肿瘤通常出现在包括上呼吸道、胃肠道和其他软组织在内的不同部位。EMP较少被探索的表现之一是颅内EMP,由于关于该主题的文献有限,人们对其了解仍然很少。目的是了解颅内EMP的人群特征、定位、类型、治疗及预后。按照系统评价和Meta分析的首选报告项目指南,对EMP的文献进行了系统评价。搜索策略为“髓外浆细胞瘤AND多发性骨髓瘤”。使用PubMed、Embase、Scopus、Cochrane和Web of Science数据库查询搜索词。我们仅纳入了那些对诊断为颅内浆细胞瘤患者的临床研究。在本研究中,共分析了来自25项研究的84例患者。诊断时的平均年龄为57.25岁,女性比例(57%)略高于男性患者(43%)。颅内浆细胞瘤最常见的部位是斜坡(29.7%)、额叶(18.9%)、顶叶(8.1%)、枕叶(6.7%)、颞叶(6.7%)和蝶骨(4%)。脊索瘤和脑膜瘤是临床检查中最常见的鉴别诊断。治疗方式包括放疗(RT)、化疗(QT)、手术切除(SR)和保守治疗方法。最常见的治疗组合是SR + RT(19%)和单纯RT(17.8%)。48%的病例报告有死亡,10例完全缓解,3例部分缓解。平均随访时间为37.5个月。斜坡是髓外颅内浆细胞瘤(EMIP)最常报道的发生部位,占病例的29.7%。脊索瘤常与EMIP一起出现,并成为主要的鉴别诊断。RT是主要的治疗方式,可行时考虑SR。单纯RT在治疗EMIP方面显示出最高的有效性(30%),而QT作为单一干预措施显示出较低的疗效。然而,地塞米松、来那度胺和靶向RT的联合应用显示出有希望的结果,提高了肿瘤反应并增加了安全性。