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喉孤立性髓外浆细胞瘤:发声障碍的一个罕见病因。

Solitary extramedullary plasmacytoma of the larynx: a rare cause of dysphonia.

机构信息

Department of Otolaryngology, Kantonsspital Aarau AG, Aarau, Switzerland.

Department of Otolaryngology, Kantonsspital Aarau AG, Aarau, Switzerland

出版信息

BMJ Case Rep. 2020 Sep 22;13(9):e234478. doi: 10.1136/bcr-2020-234478.

Abstract

Solitary extramedullary plasmacytoma (SEP) of the larynx is a rare haematological malignancy and an infrequent cause of persisting dysphonia. We present the case of a 54-year-old woman with a long-standing history of dysphonia. While clinical examination showed a rather inconspicuous prominent right vestibular fold, an MRI revealed a laryngeal mass with erosion of the thyroid cartilage. A biopsy taken during rigid endoscopy demonstrated plasma cell infiltration with light chain restriction amidst amyloid deposits. After exclusion of systemic involvement, the diagnosis of an SEP of the larynx with secondary amyloidosis was made. The patient received primary radiation therapy. Another biopsy taken 3 months after the end of therapy did not show any signs of ongoing neoplastic plasma cell disease. The patient was therefore considered to be in remission. She is currently receiving regular follow-up and has not shown signs of persistent or progressive disease for the past 18 months.

摘要

喉孤立性髓外浆细胞瘤(SEP)是一种罕见的血液系统恶性肿瘤,也是持续性发音困难的不常见病因。我们报告 1 例 54 岁女性,长期存在发音困难。临床检查显示右侧杓状软骨较为突出,但无明显异常,而 MRI 显示喉内肿块累及甲状软骨。硬质内镜下活检显示浆细胞浸润,伴有轻链限制和淀粉样物质沉积。排除系统性疾病后,诊断为伴有继发性淀粉样变性的喉 SEP。患者接受了放射治疗。治疗结束后 3 个月再次进行活检,未见肿瘤浆细胞疾病活动的迹象。因此,患者被认为处于缓解期。目前,她正在接受定期随访,在过去 18 个月中未出现持续性或进行性疾病的迹象。

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本文引用的文献

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Solitary Plasmacytoma.孤立性浆细胞瘤
Mediterr J Hematol Infect Dis. 2017 Aug 23;9(1):e2017052. doi: 10.4084/MJHID.2017.052. eCollection 2017.
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Soft tissue amyloidoma in association with plasmacytoma.
Indian J Pathol Microbiol. 2016 Oct-Dec;59(4):444-445. doi: 10.4103/0377-4929.191752.
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Clinical features and prognostic factors in solitary plasmacytoma.孤立性浆细胞瘤的临床特征和预后因素。
Br J Haematol. 2016 Feb;172(4):554-60. doi: 10.1111/bjh.13870. Epub 2015 Dec 18.

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