{"title":"A Case Report of Chondromyxoid Fibroma of the Nasal Cavity.","authors":"Jasmeet Kaur, Ankita Aggarwal, Vishav Yadav, Sanjeev Bhagat, Dinesh Sharma","doi":"10.1007/s12070-023-03981-1","DOIUrl":null,"url":null,"abstract":"<p><p>The chondromyxoid fibroma is a benign osseocartilaginous tumor histopathologically characterized by chondroid, fibrous, and myxoid tissues (Nazeer et al. in Skeltal Radiol 25:779-78, 1996). Its occurrence is quite rare, accounting for less than 0.5% of all bone tumors, with 1-5% of cases reported in the head and neck region. We report an unusual case of 25 years old male who presented with progressive swelling over dorsum of nose with bilateral nasal obstruction over 1 year. The histopathological examination was suggestive of chondromyxoid fibroma. The tumor was completely excised via open approach. We report this case owing to the rarity of the disease, sometimes masquerading as invasive/malignant pathology.</p>","PeriodicalId":17203,"journal":{"name":"Journal of The American Dietetic Association","volume":"87 12 1","pages":"3975-3979"},"PeriodicalIF":0.0000,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10645689/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The American Dietetic Association","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s12070-023-03981-1","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/6/28 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The chondromyxoid fibroma is a benign osseocartilaginous tumor histopathologically characterized by chondroid, fibrous, and myxoid tissues (Nazeer et al. in Skeltal Radiol 25:779-78, 1996). Its occurrence is quite rare, accounting for less than 0.5% of all bone tumors, with 1-5% of cases reported in the head and neck region. We report an unusual case of 25 years old male who presented with progressive swelling over dorsum of nose with bilateral nasal obstruction over 1 year. The histopathological examination was suggestive of chondromyxoid fibroma. The tumor was completely excised via open approach. We report this case owing to the rarity of the disease, sometimes masquerading as invasive/malignant pathology.
软骨粘液样纤维瘤是一种以软骨样、纤维样和粘液样组织为特征的良性骨软骨瘤(Nazeer et al. in Skeltal Radiol 25:779- 78,1996)。它的发生是相当罕见的,占所有骨肿瘤的不到0.5%,1-5%的病例报告在头颈部。我们报告一个不寻常的情况下,25岁的男性谁提出了进行性肿胀在鼻背和双侧鼻塞超过1年。组织病理学检查提示为软骨粘液样纤维瘤。经开放入路完全切除肿瘤。我们报告这个病例是因为罕见的疾病,有时伪装成侵袭性/恶性病理。