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多发性骨髓瘤侵犯前纵隔:一例报告。

Anterior mediastinum invasion by multiple myeloma: A case report.

作者信息

Xu Ying-Hui, Sun Lu-Guo, Sun Chao, Bai Ou, Liang Ting-Ting, Ma Ke-Wei

机构信息

Cancer Centre of First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.

National Engineering Laboratory for Druggable Gene and Protein Screening, Northeast Normal University, Changchun, Jilin 130024, P.R. China.

出版信息

Oncol Lett. 2017 Apr;13(4):2637-2641. doi: 10.3892/ol.2017.5756. Epub 2017 Feb 22.

Abstract

Multiple myeloma (MM) is a clonal proliferation of malignant plasma cells in the bone marrow (BM) that secretes monoclonal paraproteins in the blood serum and urine. Bone marrow MM cells can invade and damage the functions of other tissues and organs, such as the lungs, spleen, liver, pancreas, kidneys and lymph nodes. However, the invasion of MM cells primarily located in the BM to the anterior mediastinum at the site of the thymus is an extremely rare event. The current study reports the case of a 53-year-old female who presented with MM with involvement of the anterior mediastinum. The diagnosis was based on clinical imaging analyses and the results from BM and laboratory examinations, local biopsy pathology and immunohistochemistry. The patient was administered two courses of chemotherapy (epirubicin, dexamethasone and thalidomide). As a result, the tumor reduced in size, but the laboratory examination indicated no significant change. Next, the patient was switched to one course of PAD chemotherapy (bortezomib, epirubicin and dexamethasone). The original tumor was significantly reduced in size following this chemotherapy, and all the indicators improved. The present study suggests that invasion of the thymus by MM may lead to immune disturbance arising from the abnormal thymus gland. In the clinic, extramedullary plasmacytoma in the thymus should be carefully distinguished from thymoma.

摘要

多发性骨髓瘤(MM)是骨髓中恶性浆细胞的克隆性增殖,可在血清和尿液中分泌单克隆副蛋白。骨髓中的MM细胞可侵袭并损害其他组织和器官的功能,如肺、脾、肝、胰腺、肾和淋巴结。然而,主要位于骨髓的MM细胞侵袭到胸腺部位的前纵隔是极为罕见的事件。本研究报告了一例53岁女性患者,其表现为MM并累及前纵隔。诊断基于临床影像学分析、骨髓和实验室检查结果、局部活检病理及免疫组化。该患者接受了两个疗程的化疗(表柔比星、地塞米松和沙利度胺)。结果,肿瘤体积缩小,但实验室检查显示无明显变化。接下来,患者改用一个疗程的PAD化疗(硼替佐米、表柔比星和地塞米松)。此次化疗后,原发肿瘤体积显著缩小,所有指标均有所改善。本研究表明,MM侵袭胸腺可能导致胸腺异常引起免疫紊乱。临床上,胸腺中的髓外浆细胞瘤应与胸腺瘤仔细鉴别。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5647/5403540/73c2b1d0ff44/ol-13-04-2637-g00.jpg

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