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骨外浆细胞瘤:放射科医生的视角——文献综述

Extraosseous Plasmacytomas: A Radiologist's Perspective-A Narrative Review of the Literature.

作者信息

Stefanidis Konstantinos, Yusuf Gibran, Mulita Francesk, Tsalikidis Christos, Mitsala Athanasia, Konstantelou Elissavet, Kotsopoulou Maria, Koletsis Efstratios, Pitiakoudis Michail, Dimopoulos Platon

机构信息

Radiology Department, Metaxa Cancer Hospital, 18537 Piraeus, Greece.

Radiology Department, King's College Hospital NHS Foundation Trust, London SE5 9RS, UK.

出版信息

Diagnostics (Basel). 2024 Aug 16;14(16):1788. doi: 10.3390/diagnostics14161788.

DOI:10.3390/diagnostics14161788
PMID:39202276
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11353327/
Abstract

Extraosseous plasmacytomas (EPs) are rare neoplasms originating from plasma cells, often associated with multiple myeloma. EPs are classified into three subtypes: extramedullary myeloma, solitary extramedullary plasmacytoma (SEP), and multiple solitary plasmacytomas. They can manifest in various anatomical sites, including the lung, mediastinum, breast, liver, pancreas, stomach, mesentery, kidney, small and large bowel, testis, and soft tissue. Despite their rarity, EPs present a diagnostic challenge due to their non-specific imaging appearances, which can mimic other neoplastic and inflammatory conditions. This review aims to describe the radiographic features of EPs in the chest, abdomen, and pelvis based on a thorough analysis of the existing literature. While imaging plays a crucial role in the detection and characterization of EPs, histological confirmation is necessary to differentiate them from other neoplastic entities. The review underscores the importance of considering EPs in the differential diagnosis, particularly in patients with a history of multiple myeloma. Understanding the imaging characteristics of EPs is essential for accurate diagnosis and appropriate management. Early imaging is crucial in these patients to exclude the possibility of EP, as timely diagnosis can significantly impact patient outcomes.

摘要

骨外浆细胞瘤(EPs)是起源于浆细胞的罕见肿瘤,常与多发性骨髓瘤相关。EPs分为三种亚型:髓外骨髓瘤、孤立性髓外浆细胞瘤(SEP)和多发性孤立性浆细胞瘤。它们可出现在各种解剖部位,包括肺、纵隔、乳腺、肝脏、胰腺、胃、肠系膜、肾脏、小肠和大肠、睾丸以及软组织。尽管EPs罕见,但因其非特异性影像学表现可模仿其他肿瘤性和炎症性疾病,故在诊断上具有挑战性。本综述旨在通过对现有文献的全面分析,描述EPs在胸部、腹部和骨盆的影像学特征。虽然影像学在EPs的检测和特征描述中起关键作用,但组织学确诊对于将它们与其他肿瘤实体区分开来是必要的。该综述强调了在鉴别诊断中考虑EPs的重要性,特别是在有多发性骨髓瘤病史的患者中。了解EPs的影像学特征对于准确诊断和适当管理至关重要。早期影像学检查对这些患者排除EPs可能性至关重要,因为及时诊断可显著影响患者预后。

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