Mucosa-Associated Lymphoid Tissue Lymphoma of the Larynx.

IF 0.4 Q4 OTORHINOLARYNGOLOGY Case Reports in Otolaryngology Pub Date : 2020-08-18 eCollection Date: 2020-01-01 DOI:10.1155/2020/8703921
Omar Rizvi, Tyson Nielsen, Shethal Bearelly
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Abstract

Background: Mucosa-associated lymphoid tissue (MALT) lymphomas are a subtype of non-Hodgkin lymphoma stemming from marginal zone B-cells. In this case report, we present two patients with an extremely rare localization of MALT lymphoma to the larynx.

Methods: Case 1 is of a 78-year-old male presenting with a six-month history of progressive hoarseness with a past medical history significant for marginal zone lymphoma of the right orbit. Diagnosis was confirmed with a biopsy for extranodal marginal zone B-cell lymphoma of MALT type. An FDG-PET scan was done but did not show any sign of FDG avid malignancy, including at the primary site. Case 2 is a 60-year-old female presenting with one year of worsening throat discomfort, intermittent cough, and dyspnea with exertion. Pathology confirmed a diagnosis of extranodal marginal zone B-cell lymphoma of MALT type.

Results: Case 1 was treated with low-dose radiation at 4 Gy delivered over two fractions of 2 Gy each. Upon completion of radiation treatment, he reported a resolution of his hoarseness and normalization of his voice. A four-month follow-up in May 2018 with flexible nasolaryngoscopy revealed a normal exam with fully mobile vocal folds bilaterally and no evidence of left false vocal fold submucosal mass. At seven months following treatment, the patient died unexpectedly of unknown causes. Case 2 was treated with radiation at 30 Gy in 15 fractions over the course of one month. Following completion of radiation therapy, she had improvement of her sore throat, nausea, dysphagia, dysgeusia, and dry mouth. At 21-month follow-up, she had no evidence of disease.

Conclusion: This case report demonstrates that MALT lymphoma can present with much more benign and subtle symptoms. This highlights the importance of clinicians to keep broad differentials and consider MALT lymphomas in the setting of laryngeal masses.

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喉黏膜相关淋巴组织淋巴瘤。
背景:粘膜相关淋巴组织(MALT)淋巴瘤是非霍奇金淋巴瘤的一种亚型,源于边缘区B细胞。在本病例报告中,我们介绍了两名极为罕见的喉部 MALT 淋巴瘤患者:病例 1 是一名 78 岁的男性,有 6 个月的进行性声音嘶哑病史,既往病史显示其右侧眼眶边缘区淋巴瘤。经活检确诊为 MALT 型结节外边缘区 B 细胞淋巴瘤。进行了 FDG-PET 扫描,但未显示任何 FDG 阳性恶性肿瘤的迹象,包括原发部位。病例 2 是一名 60 岁的女性,一年前出现咽喉不适、间歇性咳嗽和用力呼吸困难。病理确诊为 MALT 型结外边缘区 B 细胞淋巴瘤:病例 1 接受了低剂量放射治疗,剂量为 4 Gy,分两次进行,每次 2 Gy。放疗结束后,他报告说声音嘶哑得到缓解,嗓音恢复正常。2018 年 5 月,他接受了为期四个月的随访,灵活鼻喉镜检查显示检查结果正常,双侧声带完全活动,未发现左侧假声带粘膜下肿块。治疗七个月后,患者因不明原因意外死亡。病例 2 在一个月内接受了 15 次 30 Gy 的放射治疗。放疗结束后,她的咽喉痛、恶心、吞咽困难、发音障碍和口干症状有所改善。在 21 个月的随访中,她没有发现任何疾病迹象:本病例报告表明,MALT 淋巴瘤可表现为良性和细微的症状。结论:本病例报告表明,MALT淋巴瘤可表现为更为良性和隐匿的症状,这突出了临床医生在发现喉肿块时保持广泛鉴别并考虑MALT淋巴瘤的重要性。
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来源期刊
Case Reports in Otolaryngology
Case Reports in Otolaryngology OTORHINOLARYNGOLOGY-
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发文量
20
审稿时长
13 weeks
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