Subglottic Inflammatory Myofibroblastic Tumor in a Child: A Rare Case Report.

Ahmad Alkheder, Yasser Al-Ghabra, Adel Azar, Ahmad Dmirieh, Adham Bader Aldeen Mohsen, Abdulmajeed Yousfan
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Abstract

Inflammatory myofibroblastic tumor (IMT) is an uncommon mesenchymal neoplasm rarely encountered in the pediatric larynx, with the subglottis representing an atypical subsite. This report details a diagnostically instructive case of a 10-year-old girl presenting with 18 months of progressive dyspnea and exertional stridor, notably without hoarseness. Fibroendoscopic laryngoscopy identified a well-circumscribed right subglottic mass, confirmed on computed tomography scan to cause partial airway narrowing. The lesion's firm intraoperative consistency contrasted with common benign mimics. Histopathology revealed spindle cell proliferation with mixed inflammation (histiocytes, giant cells), while immunohistochemistry demonstrated focal anaplastic lymphoma kinase (ALK) and smooth muscle actin (SMA) positivity, CD68+ histiocytes, and CD1A negativity-collectively confirming IMT and excluding Langerhans cell histiocytosis. Complete endoscopic excision was achieved. This case underscores critical learning points: (1) IMT must be considered in children with progressive stridor/dyspnea, even lacking hoarseness, particularly with subglottic localization, and firm consistency; (2) Subglottic IMTs primarily manifest airway obstruction rather than voice changes typical of glottic lesions; (3) Focal ALK expression, present here, supports clonality but does not preclude a favorable outcome with complete resection; and (4) Immunohistochemistry (ALK/SMA/CD68/CD1A) is indispensable for accurate diagnosis and avoiding misdirected therapy. Despite excellent early postoperative results consistent with the generally favorable prognosis of pediatric IMT, vigilance for recurrence-highest within the first 2 years-remains essential. This report reinforces complete conservative resection as the cornerstone of management for localized disease, reserving adjuvant therapies for complex or recurrent scenarios. Multidisciplinary collaboration optimizes outcomes while preserving laryngeal integrity in children.

儿童声门下炎性肌成纤维细胞瘤:罕见病例报告。
炎症性肌纤维母细胞瘤(IMT)是一种罕见的间充质肿瘤,很少在儿童喉部遇到,声门下是一个不典型的亚区。本报告详细介绍了一个诊断上有指导意义的病例,一名10岁的女孩,表现为18个月的进行性呼吸困难和用力喘气,特别是没有声音嘶哑。纤维内窥镜喉镜检查发现一个界限清晰的右侧声门下肿块,在计算机断层扫描上证实引起部分气道狭窄。术中病变与常见的良性相似病变形成对比。组织病理学显示梭形细胞增生并伴有混合炎症(组织细胞,巨细胞),而免疫组织化学显示局灶间变性淋巴瘤激酶(ALK)和平滑肌肌动蛋白(SMA)阳性,CD68+组织细胞,CD1A阴性-共同证实IMT,排除朗格汉斯细胞组织细胞增多症。完成了内镜下的完全切除。该病例强调了关键的学习要点:(1)对于进行性喘鸣/呼吸困难的儿童,即使没有声音嘶哑,特别是声门下定位和坚定的一致性,也必须考虑IMT;(2)声门下IMTs主要表现为气道阻塞,而不是声门病变典型的声音改变;(3)局灶性ALK表达支持克隆,但不排除完全切除的有利结果;(4)免疫组织化学(ALK/SMA/CD68/CD1A)对于准确诊断和避免错误治疗是必不可少的。尽管儿童IMT的早期术后效果良好,预后良好,但警惕复发(最高在前2年)仍然是必要的。本报告强调完全保守切除是局部疾病治疗的基石,对于复杂或复发的情况保留辅助治疗。多学科合作优化结果,同时保留喉完整性的儿童。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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