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本文引用的文献

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Extramedullary plasmacytoma of the orbit with intracranial invasion: A case report.眼眶内侵犯的骨髓外浆细胞瘤：一例报告。
Medicine (Baltimore). 2023 Jun 16;102(24):e33920. doi: 10.1097/MD.0000000000033920.
2
A Case Series of Aggressive Orbital Plasmacytomas.侵袭性眼眶浆细胞瘤病例系列
Ocul Oncol Pathol. 2023 Feb;8(4-6):197-202. doi: 10.1159/000527273. Epub 2022 Oct 12.
3
Spheno-Orbital Plasmacytoma as an Initial Presentation of Multiple Myeloma.蝶眶浆细胞瘤作为多发性骨髓瘤的首发表现
Brain Tumor Res Treat. 2022 Oct;10(4):270-274. doi: 10.14791/btrt.2022.0026.
4
Radiologic manifestations of primary solitary extramedullary and multiple solitary plasmacytomas.原发性孤立性髓外浆细胞瘤和多发性孤立性浆细胞瘤的放射学表现。
AJR Am J Roentgenol. 2006 Mar;186(3):821-7. doi: 10.2214/AJR.04.1787.
5
Guidelines on the diagnosis and management of solitary plasmacytoma of bone and solitary extramedullary plasmacytoma.骨孤立性浆细胞瘤和孤立性髓外浆细胞瘤的诊断与管理指南
Clin Oncol (R Coll Radiol). 2004 Sep;16(6):405-13. doi: 10.1016/j.clon.2004.02.007.

一名老年多发性骨髓瘤患者的眼眶浆细胞瘤

Orbital Plasmacytoma in an Elderly Patient With Multiple Myeloma.

作者信息

Aloui Salma, Qureshi Pir Abdul Ahad Aziz, Bollineni Vikram Rao

机构信息

Department of Radiology, Universitair Ziekenhuis Brussel, Brussels, BEL.

Department of Radiology, Landspítali - The National University Hospital of Iceland, Reykjavík, ISL.

出版信息

Cureus. 2024 Feb 8;16(2):e53823. doi: 10.7759/cureus.53823. eCollection 2024 Feb.

DOI:10.7759/cureus.53823
PMID:38465072
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10924626/
Abstract

Orbital plasmacytomas are exceedingly rare neoplasms characterized by the proliferation of monoclonal plasma cells in the orbital soft tissues. Their presentation and clinical course can be diverse, making early diagnosis and management challenging. This case report sheds light on one such instance, emphasizing the diagnostic and therapeutic aspects of this uncommon condition. We present an 81-year-old patient with a prior diagnosis of multiple myeloma and bilateral orbital plasmacytomas, highlighting the importance of imaging in diagnosis and management.

摘要

眼眶浆细胞瘤是极其罕见的肿瘤，其特征为眼眶软组织中克隆性浆细胞增殖。它们的表现和临床病程可能多种多样，使得早期诊断和治疗具有挑战性。本病例报告揭示了这样一个实例，强调了这种罕见病症的诊断和治疗方面。我们报告一名81岁的患者，此前诊断为多发性骨髓瘤和双侧眼眶浆细胞瘤，突出了影像学在诊断和治疗中的重要性。