Inflammatory Myofibroblastic Tumor of the Subglottis: A Rare Case Report.

IF 1 4区 医学 Q3 OTORHINOLARYNGOLOGY Ent-Ear Nose & Throat Journal Pub Date : 2025-02-01 Epub Date: 2022-05-09 DOI:10.1177/01455613221083810
Zhe Chen, Wei Xiao, Tao Peng, Linfeng Ye
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Abstract

Inflammatory myofibroblastic tumor (IMT) is a very rare mesenchymal tumor that can behave as a locally benign or aggressive lesion. Here, we present an extremely rare case of IMT involving the subglottic of a middle-aged male. Steroid therapy treatment alleviated dyspnea, but the recurrence of dyspnea was reported two months later. Both sides of the subglottic tumor were excised following treatment, and the surgical specimens were subjected to histopathological evaluation and diagnosis for IMT. At 4 years after excision, follow-up laryngoscopy revealed symmetric vocal cords without evidence of any subglottic mass. Subglottic mass is often asymptomatic until it presents with hoarseness or dyspnea, and subglottic IMT is rare. Based on the successful treatment of our case, complete surgical excision is highly recommended for this rare tumor. However, further research is needed to discover a more effective and cost-effective treatment approach.

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声门下炎性肌成纤维细胞瘤:一罕见病例报告。
炎性肌纤维母细胞瘤(IMT)是一种非常罕见的间充质肿瘤,可表现为局部良性或侵袭性病变。在这里,我们提出一个极其罕见的病例IMT涉及声门下的中年男性。类固醇治疗缓解了呼吸困难,但两个月后再次出现呼吸困难。治疗后切除双侧声门下肿瘤,手术标本行组织病理学评估和IMT诊断。术后4年,随访喉镜检查显示声带对称,无声门下肿块。声门下肿块通常无症状,直到它表现为声音嘶哑或呼吸困难,声门下肿块是罕见的。基于我们病例的成功治疗,我们强烈建议对这种罕见的肿瘤进行完全的手术切除。然而,需要进一步的研究来发现更有效和更具成本效益的治疗方法。
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来源期刊
Ent-Ear Nose & Throat Journal
Ent-Ear Nose & Throat Journal 医学-耳鼻喉科学
CiteScore
3.20
自引率
0.00%
发文量
385
审稿时长
6-12 weeks
期刊介绍: Ear, Nose & Throat Journal provides practical, peer-reviewed original clinical articles, highlighting scientific research relevant to clinical care, and case reports that describe unusual entities or innovative approaches to treatment and case management. ENT Journal utilizes multiple channels to deliver authoritative and timely content that informs, engages, and shapes the industry now and into the future.
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