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首页> 外文期刊>Case Reports in Otolaryngology >Mucosa-Associated Lymphoid Tissue Lymphoma of the Larynx
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Mucosa-Associated Lymphoid Tissue Lymphoma of the Larynx

机译:粘膜相关淋巴结组织淋巴瘤

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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.
机译:背景。粘膜相关淋巴组织(麦芽)淋巴瘤是来自边缘区B细胞的非霍奇金淋巴瘤的亚型。在本例报告中,我们提出了两名患有极少数麦芽淋巴瘤本地化的患者到喉部。方法。案例1是一个78岁的男性,呈现六个月的逐步嘶哑的历史,与过去轨道边缘区淋巴瘤的过去的医学史。用麦芽型B细胞淋巴瘤的活检确认了诊断。完成了FDG-PET扫描,但没有显示FDG Avid Malignancy的任何迹象,包括在主要网站上。案例2是一名60岁的女性,患有一年的喉咙不适,间歇性咳嗽和呼吸困难。病理学证实了麦芽型外胚间区域B细胞淋巴瘤的诊断。结果。案例1在4μl的低剂量辐射处理,每次递送2μm的两部分。在完成辐射治疗后,他报告了他对其声音的嘶哑和正常化的解决方案。 2018年5月,柔性鼻阳镜镜检查了一个为期四个月的随访,揭示了正常的考试,与完全移动的声乐双侧,没有证据左虚假折叠粘膜脓肿。治疗后七个月后,病人意外地死于未知的原因。案例2在15个级数在一个月内以30μl辐射治疗。完成放射疗法后,她有改善她的喉咙痛,恶心,吞咽困难,痛苦乌西亚和口干。在21个月的随访中,她没有疾病的证据。结论。本病例报告表明,麦芽淋巴瘤可以带来更良好的良性和微妙的症状。这突显了临床医生在喉部群体中保持较大差异并考虑麦芽淋巴瘤的重要性。

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