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Extracardiac juvenile rhabdomyoma of the larynx: a rare pathological finding.

机译:喉外心型少年横纹肌瘤:罕见的病理发现。

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摘要

The extracardiac juvenile rhabdomyoma is extremely rare in the field of Otorhinolaryngology. The tumour usually arises from the soft tissue of the face or from mucosal sites, especially the oropharynx and the oral cavity but only sporadic endolaryngeal cases have been described in literature so far with predominance of young males. Here, we describe the very rare case of endolaryngeal extracardiac juvenile rhabdomyoma in a 42-year-old male. Clinical examination showed a mass of the right vocal cord, resembling a cystic lesion. Microlaryngoscopy revealed a non-encapsulated lesion and histopathology including immunohistochemistry which consecutively led to the correct diagnosis. This case suggests that the endolaryngeal extracardiac juvenile rhabdomyoma can be easily confused with a vocal cord cyst. Malignant transformations have not been reported but recurrences have been described. When total excision cannot be accomplished, reoperation or narrow follow-up is indicated to prevent advanced revision surgeries.
机译:心外少年横纹肌瘤在耳鼻喉科学领域极为罕见。肿瘤通常起源于面部的软组织或粘膜部位,尤其是口咽和口腔,但迄今为止,文献中仅以散发性鼻咽部病例为例,主要是年轻男性。在这里,我们描述了一名42岁男性的极少见的喉内膜外青少年横纹肌瘤病例。临床检查显示右声带肿块,类似于囊性病变。微喉镜检查发现未包囊的病变和组织病理学,包括免疫组织化学,连续导致正确的诊断。这种情况表明,喉内膜外少年横纹肌瘤很容易与声带囊肿混淆。尚未报道恶性转化,但已描述了复发。当无法完全切除时,应指示再次手术或狭窄的随访,以防止进行高级翻修手术。

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