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喉软骨骨髓瘤:文献复习与病例研究。

Myeloma of Laryngeal Cartilage: Literature Review and Case Study.

机构信息

Department of Ear Nose Throat, 95145Toowoomba Base Hospital, Toowoomba, Queensland, Australia.

Department of Medical Imaging, 60093Gold Coast University Hospital, Southport, Queensland, Australia.

出版信息

Ear Nose Throat J. 2021 Feb;100(2):NP114-NP119. doi: 10.1177/0145561319861379. Epub 2019 Jul 8.

Abstract

BACKGROUND

Myeloma of laryngeal cartilage (MLC) is a rare plasma cell neoplasm which has not been well characterized. However, it is an important differential diagnosis of laryngeal cartilage mass as it can indicate the presence of underlying systemic hematological diseases, such as multiple myeloma (MM), that is associated with poor prognosis. This article is the first of its kind and aims to educate clinicians on future diagnosis and management of similar cases.

METHODS

Search of MLC was performed on the medical literature databases of Medline, PUBMED, and EMBASE. Additionally, institutional database at Gold Coast University Hospital Radiology Department was queried for relevant cases. Based on 16 cases that met the inclusion criteria, the etiology, epidemiology, clinical evaluation, investigations, management, and prognosis of MLC was summarized.

RESULTS

Of all, 94% of MLC occur in males and 81% in those older than 60 years. It is more commonly a manifestation of systemic MM, rather than localized extramedullary plasmacytoma (EMP), 81% and 19% respectively. Additionally, 67% of laryngeal EMPs progress to MM within 3 years from initial diagnosis. Although treatments involving both local and systemic therapy were effective at relieving local symptoms, 39% of MLC patients died during the follow-up period-all of which were due to septicemia caused by secondary infections.

CONCLUSION

Myeloma of laryngeal cartilage is a relatively rare condition that requires accurate diagnosis in order to promptly manage the potentially underlying systemic hematological disease. Currently, more case reports and analytical studies are required to provide evidence-based guidance on etiology, diagnosis, and management of this condition.

摘要

背景

喉软骨骨髓瘤(MLC)是一种罕见的浆细胞瘤,尚未得到充分描述。然而,由于它是喉软骨肿块的重要鉴别诊断,因为它可能表明存在潜在的系统性血液病,如多发性骨髓瘤(MM),其预后不良。本文是此类文章中的首例,旨在为临床医生提供未来类似病例的诊断和管理。

方法

在 Medline、PUBMED 和 EMBASE 的医学文献数据库中进行了 MLC 的搜索。此外,还在黄金海岸大学医院放射科的机构数据库中查询了相关病例。根据符合纳入标准的 16 例病例,总结了 MLC 的病因、流行病学、临床评估、检查、治疗和预后。

结果

所有病例中,94%的 MLC 发生在男性,81%发生在 60 岁以上的人群。它更常见于系统性 MM 的表现,而不是局部髓外浆细胞瘤(EMP),分别为 81%和 19%。此外,67%的喉 EMP 在初始诊断后 3 年内进展为 MM。尽管局部和全身治疗均能有效缓解局部症状,但仍有 39%的 MLC 患者在随访期间死亡,这均归因于继发感染引起的败血症。

结论

喉软骨骨髓瘤是一种相对罕见的疾病,需要准确诊断,以便及时处理潜在的系统性血液病。目前,需要更多的病例报告和分析研究,为该疾病的病因、诊断和治疗提供循证指导。

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