El-Kouri Nadeem, Elghouche Alhasan, Chen Shaoxiong, Shipchandler Taha, Ting Jonathan
Department of Otolaryngology - Head and Neck Surgery, Loyola University Chicago Stritch School of Medicine, Maywood, USA.
Department of Medical Education and Simulation, Indiana University School of Medicine, Indianapolis, USA.
Cureus. 2019 Oct 5;11(10):e5841. doi: 10.7759/cureus.5841.
Chondromyxoid fibroma (CMF) is a rare, benign neoplasm of the chondroid, myxoid, and fibrous tissue. It characteristically affects the lower extremity long bones, although it may rarely arise within the craniofacial skeleton. We report the diagnosis and management of a 31-year-old male with a large, incidentally discovered CMF originating from the sphenoid sinus. A subsequent review of the literature reveals the need to differentiate from more aggressive neoplasms, such as chondrosarcoma and chondroma, which share radiographic features. A histopathologic examination is crucial for proper diagnosis and treatment. We discuss clinical sequelae, highlight the importance of a thorough pre-operative evaluation, and summarize previously suggested treatment paradigms.
软骨黏液样纤维瘤(CMF)是一种罕见的由软骨样、黏液样和纤维组织构成的良性肿瘤。其特征性地累及下肢长骨,不过也可能极少发生于颅面骨骼。我们报告了一名31岁男性的诊断及治疗情况,该患者偶然发现一个源自蝶窦的巨大CMF。随后的文献回顾显示,有必要与具有相似影像学特征的更具侵袭性的肿瘤,如软骨肉瘤和软骨瘤相鉴别。组织病理学检查对于正确诊断和治疗至关重要。我们讨论了临床后遗症,强调了全面术前评估的重要性,并总结了先前提出的治疗模式。