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最初表现为蝶窦、眶尖和颅底的免疫球蛋白D-λ多发性骨髓瘤:一项病例报告的系统评价

Immunoglobulin D-Lambda Multiple Myeloma Initially Presenting in the Sphenoid Sinus, Orbital Apex, and Skull Base: A Systematic Review with a Case Report.

作者信息

Chen Yihan, Liu Jianfeng, Zhao Jianhui

机构信息

China-Japan Friendship Hospital, Beijing University of Chinese Medicine, Beijing, People's Republic of China.

Department of Otolaryngology-Head and Neck Surgery, China-Japan Friendship Hospital, Beijing, People's Republic of China.

出版信息

J Neurol Surg Rep. 2024 Sep 16;85(3):e144-e155. doi: 10.1055/s-0044-1790589. eCollection 2024 Jul.

DOI:10.1055/s-0044-1790589
PMID:39355801
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11444811/
Abstract

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  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.  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.  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.

摘要

首发于蝶窦、眶尖和颅底的多发性骨髓瘤(MM)极为罕见。我们进行了一项系统综述,以调查其流行病学和进展情况。通过检索中国知网、万方数据、维普数据库、PubMed、Embase和Web of Science来确定相关病例。此外,我们报告了一例IgD-λ(免疫球蛋白D-λ)型MM病例,其初始症状为头晕、单侧疼痛、失明和眼肌麻痹,总生存期为4个月。严格按照PRISMA标准,我们纳入并总结了现有病例,并呈现了我们的病例。我们的系统综述纳入了34篇病例报告,显示67.6%的患者最初表现为复视,44.1%的患者接受了内镜手术,其中IgD-λ亚型仅有两例。在我们的病例中,我们进行了内镜下经筛窦扩大蝶窦切开术,并对颅底和眶尖病变进行了活检。术后病理证实为高度活跃的浆细胞瘤,临床诊断为IgD-λ型MM,伴有TP53缺失突变和多处髓外转移。我们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)、骨髓细胞学检查和基因检测。IgD-λ型MM在鼻窦和颅底的临床表现隐匿,不利于早期诊断。关于MM最初出现在这些部位的文献较少。CT/磁共振扫描对于识别特征性骨质破坏很有必要。内镜检查是组织活检的常用方法。一旦出现靶器官损害,骨髓涂片活检、血清或尿蛋白电泳以及免疫固定电泳至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bf6/11444811/a606d2913eb4/10-1055-s-0044-1790589-i24jul0034-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bf6/11444811/b2a4e7095473/10-1055-s-0044-1790589-i24jul0034-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bf6/11444811/25d5f848c122/10-1055-s-0044-1790589-i24jul0034-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bf6/11444811/a606d2913eb4/10-1055-s-0044-1790589-i24jul0034-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bf6/11444811/b2a4e7095473/10-1055-s-0044-1790589-i24jul0034-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bf6/11444811/25d5f848c122/10-1055-s-0044-1790589-i24jul0034-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bf6/11444811/a606d2913eb4/10-1055-s-0044-1790589-i24jul0034-3.jpg

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本文引用的文献

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Case Report: Cavernous Sinus Syndrome as the Initial Presentation of Multiple Myeloma.病例报告:海绵窦综合征作为多发性骨髓瘤的首发表现
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Multiple myeloma with plasmacytoma of the clivus bone presenting with multiple cranial nerve III, IV, and VI palsy: A diagnostic dilemma.
伴有斜坡骨浆细胞瘤的多发性骨髓瘤表现为动眼神经、滑车神经和展神经多发麻痹:诊断难题。
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