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Systemic lupus erythematosus in a patient with primary MALT lymphoma of the larynx.

作者信息

Gonzàlez Núria, Xicoy Blanca, Olivé Alejandro, Jové Josep, Ribera Josep-Maria, Feliu Evarist

机构信息

Clinical Hematology Department, Institut Català d'Oncologia, Hospital Germans Trias i Pujol, Badalona, Universitat Autònoma de Barcelona, Spain.

出版信息

Ear Nose Throat J. 2009 Aug;88(8):E4-5.

PMID:19688705
Abstract

Primary lymphomas of the larynx are extremely rare. Even more unusual is their association with rheumatologic diseases. Some cases of lymphoma have developed after chemotherapy for rheumatologic diseases, suggesting that the treatment may contribute to the development of lymphoma. The converse can also occur-the development of rheumatologic disease after a primary laryngeal lymphoma-but that is even rarer. We report a case of primary extranodal marginal zone B-cell MALT (mucosa-associated lymphoid tissue)lymphoma of the larynx in a 42-year-old woman treated with involved-field radiotherapy who developed systemic lupus erythematosus (SLE) 1 year after the lymphoma diagnosis. Currently, the patient remains in remission 8 years after her diagnosis. The SLE, for which she is receiving maintenance therapy, is stable.

摘要

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引用本文的文献

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Mucosa-associated lymphoid tissue lymphoma of the larynx: a case report and literature review.喉黏膜相关淋巴组织淋巴瘤:一例报告及文献复习
Medicine (Baltimore). 2015 May;94(17):e788. doi: 10.1097/MD.0000000000000788.
2
A Case of a Laryngeal MALT Lymphoma in a Patient with a History of Gastric MALT.一例有胃黏膜相关淋巴组织淋巴瘤病史患者的喉黏膜相关淋巴组织淋巴瘤病例。
Case Rep Hematol. 2015;2015:109561. doi: 10.1155/2015/109561. Epub 2015 Jan 18.