A Rare Case of Spontaneous Regression of Laryngeal Amyloidosis.

IF 2.4 4区 医学 Q1 AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY
Talitha Kumaresan Lewis, Denis Lafreniere, Poornima Hegde
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引用次数: 0

Abstract

Objective: To review a rare case of spontaneous regression of laryngeal amyloidosis and current management of the disease.

Introduction: While laryngeal amyloidosis is rare (<1% of benign laryngeal lesions), it is the most common site of localized head and neck amyloidosis. The most common presenting symptoms include dysphonia and dyspnea. The mainstay of treatment is surgical excision. We report a rare case of spontaneously regressing laryngeal amyloidosis, which has not been previously reported in the literature to the best of the authors' knowledge.

Methods: Single case study.

Results: We report the case of an 82-year-old male recently diagnosed with rheumatoid arthritis on methotrexate who presented with 6 months of dysphonia and significant worsening over the past month. Flexible laryngoscopy revealed an irregular mass of the right true vocal cord with hypomobility. Given concern for possible malignancy, a CT scan was obtained, which revealed a multilobulated soft tissue mass of the right true vocal cord with 15 mm caudal extension into the subglottic airway. Pathology was consistent with amyloidosis. Hematology workup revealed no systemic involvement. Subsequent laryngoscopy two months later demonstrated spontaneous regression of 85% of the lesion and return of normal vocal cord mobility. Given significant improvement, surgical intervention was deferred for surveillance monitoring. Eight months after the initial presentation, the patient's dysphonia and lesion continue to regress.

Conclusion: While laryngeal amyloidosis is rare (<1% of benign laryngeal lesions), it is the most common site of localized head and neck amyloidosis. We report a rare case of spontaneously regressing laryngeal amyloidosis, which has not been previously reported in the literature to the best of the authors' knowledge. This is a rare phenomenon as laryngeal amyloidosis typically requires surgical excision. As this case highlights, localized laryngeal amyloidosis has favorable outcomes, but diligent surveillance is required given the risk of recurrence.

喉淀粉样变自发性消退1例。
目的:回顾1例喉淀粉样变自发性消退及治疗现状。简介:喉淀粉样变性罕见(方法:单例研究。结果:我们报告一例82岁的男性最近诊断为类风湿关节炎的甲氨蝶呤谁提出了6个月的语音障碍和显着恶化在过去的一个月。软性喉镜检查显示右侧真声带不规则肿块伴低活动能力。考虑到可能的恶性肿瘤,CT扫描显示右侧真声带多分叶软组织肿块,并向声门下气道延伸15毫米。病理表现与淀粉样变一致。血液学检查未发现全身受累。两个月后的喉镜检查显示85%的病变自发消退,声带活动恢复正常。鉴于明显改善,手术干预推迟进行监测。首次出现后8个月,患者的发音障碍和病变继续消退。结论:喉淀粉样变少见(
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来源期刊
Journal of Voice
Journal of Voice 医学-耳鼻喉科学
CiteScore
4.00
自引率
13.60%
发文量
395
审稿时长
59 days
期刊介绍: The Journal of Voice is widely regarded as the world''s premiere journal for voice medicine and research. This peer-reviewed publication is listed in Index Medicus and is indexed by the Institute for Scientific Information. The journal contains articles written by experts throughout the world on all topics in voice sciences, voice medicine and surgery, and speech-language pathologists'' management of voice-related problems. The journal includes clinical articles, clinical research, and laboratory research. Members of the Foundation receive the journal as a benefit of membership.
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