Suppr超能文献

系统性红斑狼疮合并多发性骨髓瘤:两例病例报告及文献复习。

Systemic lupus erythematosus associated with multiple myeloma: Two case reports and a literature review.

机构信息

Department of Rheumatology & Immunology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.

出版信息

Immun Inflamm Dis. 2023 Jan;11(1):e755. doi: 10.1002/iid3.755.

Abstract

INTRODUCTION

Systemic lupus erythematosus (SLE) complicated by multiple myeloma (MM) is a relatively rare clinical presentation, and is easily ignored due to their similar or even identical manifestation, which may lead to misdiagnosis and mistreatment.

CASE REPORT

We report two cases of SLE with MM. Case 1 was a 59-year-old male who was diagnosed with SLE 11 years ago. Abnormal kidney function was detected 4 months ago and a bone marrow aspirate revealed MM. He then received three cycles of bortezomib, dexamethasone, and chemotherapy with liposomal doxorubicin, and one cycle of lenalidomide plus dexamethasone. He died of infectious shock. Case 2 was a 58-year-old female who was diagnosed with SLE 27 years ago. After the onset of abnormal renal function 4 years ago, the patient was still treated according to SLE disease activity. When renal function rapidly deteriorated, serum and urine immunofixation electrophoresis was positive for IgG γ with free light chains and she was diagnosed with SLE complicated by MM. She did not agree to the treatment for MM as advised and was discharged from the hospital against medical advice. Case 2 died of cardiac failure. Thirteen cases of SLE with MM reported from 2000 to 2022 in PUBMED and Mendeley and our above two cases were reviewed. Among the 15 patients, 13 were females and 2 were males. The median age at the time of SLE with MM diagnosis was 50 years, and the median time to a delayed diagnosis was 7 years. The serum monoclonal immunoglobulin level was elevated and extramedullary manifestations of renal dysfunction were common.

CONCLUSIONS

An elevated monoclonal immunoglobulin level or newly unexplained renal dysfunction occurring in a patient with SLE should prompt monitoring and further screening of MM, rather than treatment as a secondary manifestation of SLE.

摘要

简介

红斑狼疮(SLE)并发多发性骨髓瘤(MM)是一种相对罕见的临床表现,由于其表现相似甚至相同,容易被忽视,从而导致误诊和误治。

病例报告

我们报告两例 SLE 合并 MM 的病例。例 1 为 59 岁男性,11 年前诊断为 SLE。4 个月前发现肾功能异常,骨髓穿刺显示 MM。随后接受了硼替佐米、地塞米松和脂质体阿霉素化疗 3 个周期,以及来那度胺联合地塞米松化疗 1 个周期。患者死于感染性休克。例 2 为 58 岁女性,27 年前诊断为 SLE。4 年前肾功能异常发作后,仍按 SLE 疾病活动度治疗。肾功能迅速恶化时,血清和尿液免疫固定电泳 IgGγ 阳性,游离轻链阳性,诊断为 SLE 并发 MM。患者不同意建议的 MM 治疗方案并出院,后死于心力衰竭。我们对 2000 年至 2022 年 PUBMED 和 Mendeley 报道的 13 例 SLE 合并 MM 病例和上述两例进行了回顾性分析。15 例患者中,女性 13 例,男性 2 例。SLE 合并 MM 诊断时的中位年龄为 50 岁,中位延迟诊断时间为 7 年。血清单克隆免疫球蛋白水平升高,肾功能不全的髓外表现常见。

结论

SLE 患者出现单克隆免疫球蛋白水平升高或新出现的不明原因的肾功能不全时,应及时监测并进一步筛查 MM,而不是按 SLE 的次要表现进行治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49ee/9803932/30259eeefdc0/IID3-11-e755-g003.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验