鼻软骨间充质错构瘤:1例成人报告

Mehdi Askari, M. Kadivar, S. Mohebbi, Ghazal Zoghi
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摘要

背景:鼻软骨间充质错构瘤(NCMH)是一种罕见的良性肿瘤,几乎常见于儿童。1998年,McDermott首次描述了NCMH。据我们所知,全世界已报告了约50例非传染性cmh病例,其中很少有成人病例,也没有长期随访。病例介绍:在这里,我们报告了一名43岁的女性,她于2008年转诊到伊朗阿巴斯港Payambar Azam医院耳鼻喉科诊所,她有一年的进行性左侧鼻塞病史,局部使用减充血剂和类固醇喷雾剂后仍未缓解。检查发现单侧左侧鼻软组织肿块。组织学和免疫组织化学分析与NCMH一致。经鼻内镜切除效果良好,随访12年无复发迹象。结论:了解NCMH的影像学和免疫组织化学特征,结合成人出现的概率,对正确诊断和适当治疗是必要的。
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Nasal Chondromesenchymal Hamartoma: An Adult Case Report
Background: Nasal chondromesenchymal hamartoma (NCMH) is a rare benign tumor almost always found in children. NCMH was first described by McDermott in 1998. To the best our knowledge, about 50 NCMH cases have been reported worldwide with very few adult cases and no long-term follow-ups. Case Presentation: Here, we report a 43-year-old woman who referred to the Otolaryngology Clinic of Payambar Azam Hospital, Bandar Abbas, Iran, in 2008, with a one-year history of progressive left-sided nasal obstruction that had not relieved with topical nasal decongestants and steroid sprays. A unilateral left-sided nasal soft-tissue mass was found upon examination. Histological and immunohistochemical analyses were consistent with NCMH. Trans-nasal endoscopic excision showed good results and no sign of recurrence has been observed after 12 years of regular follow-up. Conclusion: Awareness of imaging and immunohistochemical characteristics of NCMH combined with the probability of presentation in the adult population are necessary for correct diagnosis and adequate therapy.
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