最初出现在蝶窦、眶顶和颅底的免疫球蛋白D-Lambda多发性骨髓瘤:系统回顾与病例报告。

IF 0.6 Q4 CLINICAL NEUROLOGY
Journal of Neurological Surgery Reports Pub Date : 2024-09-16 eCollection Date: 2024-07-01 DOI:10.1055/s-0044-1790589
Yihan Chen, Jianfeng Liu, Jianhui Zhao
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引用次数: 0

摘要

目标 最初表现在蝶窦、眶顶和颅底的多发性骨髓瘤(MM)极为罕见。本研究对其流行病学和研究进展进行了系统回顾。方法 通过检索 CNKI、万方数据、CQVIP 数据库、PubMed、Embase 和 Web of Science 来确定相关病例。此外,我们还发现了一例 IgD-λ(免疫球蛋白 D-lambda)MM,其最初症状为头晕、单侧疼痛、失明和眼球震颤,最终获得了 4 个月的总生存期。我们严格按照 PRISMA 标准纳入并总结了现有病例,并反映了我们的病例。结果 我们的系统综述包括 34 篇病例报告,发现 67.6% 的患者最初表现为复视,44.1% 的患者接受了内窥镜手术,其中只有两例为 IgD-λ 亚型。在我们的病例中,我们在内镜下进行了宽大的经蝶窦蝶窦切除术,并对颅底和眶顶病灶进行了活检。术后病理证实为高活性浆细胞瘤,临床诊断为IgD-λ MM,伴有TP53缺失突变和多发性髓外转移。采用了一系列诊断工具,包括血红蛋白、免疫球蛋白、尿蛋白分析、正电子发射断层扫描-计算机断层扫描(CT)、骨髓细胞学和基因检测。结论 鼻旁窦和颅底 IgD-λ MM 的临床表现不明显,妨碍了早期诊断。描述最初出现在这些部位的 MM 的文献很少。CT/磁共振扫描是确定特征性骨质破坏的必要手段。组织活检常用内窥镜方法。骨髓活检涂片、血清或尿蛋白电泳以及免疫固定电泳在出现靶器官损害时至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunoglobulin D-Lambda Multiple Myeloma Initially Presenting in the Sphenoid Sinus, Orbital Apex, and Skull Base: A Systematic Review with a Case Report.

Objectives  Multiple myeloma (MM) with initial manifestations in the sphenoid sinus, orbital apex, and skull base is exceedingly rare. A systematic review was conducted to investigate the epidemiology and advancements . Methods  Relevant cases were identified by searching CNKI, WanFang Data, CQVIP databases, PubMed, Embase, and Web of Science. Additionally, we present a case of IgD-λ (immunoglobulin D-lambda) MM with initial symptoms of dizziness, unilateral pain, blindness, and ophthalmoplegia, leading to a 4-month overall survival. Strictly based on PRISMA standards, we included and summarized existing cases and reflected our case. Results  Our systematic review includes 34 case reports, revealing 67.6% of patients initially presented with diplopia and 44.1% underwent endoscopic procedures, notably with only two cases of IgD-λ subtype. In our case, we performed an endoscopic wide trans-ethmoidal sphenoidotomy and biopsy of the skull base and orbital apex lesion. Postoperative pathology confirmed a highly active plasmacytoma, clinically diagnosed as IgD-λ MM with a TP53 deletion mutation and multiple extramedullary metastases. A range of diagnostic tools was employed, including hemoglobin, immunoglobulin, urinary protein analysis, positron emission tomography-computed tomography (CT), bone marrow cytology, and gene detection. Conclusion  The subtle clinical manifestations of IgD-λ MM in the paranasal sinuses and skull base hinder early diagnosis. There is a paucity of literature describing MM initially presenting in these locations. CT/magnetic resonance scans are necessary to identify characteristic bone destruction. An endoscopic approach is popular for tissue biopsy. Bone marrow biopsy with a smear, serum or urine protein electrophoresis, and immunofixation electrophoresis are crucial upon the appearance of target organ damage.

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