Chondromyxoid fibroma in the oro-facial region: A case report

H.M. Shahriar Rubel , Mustari Nailah Tabassum , Sadia Sultana Imla , Arpita Biswangree , Esrat Jahan
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Abstract

Chondromyxoid Fibroma (CMF) is an uncommon, slow-growing benign chondroblast tumour with hypocellular or chondromyxoid tissue and multinucleated cells. Similar pathologies to aggressive tumours, such as chondrosarcoma, make CMFs harder to identify. This lesion may cause painful swelling or enlargement for weeks or years or may be identified accidentally during radiological scanning. A 24-year-old girl was diagnosed with CMF affecting the right upper jaw. She came with a developing mass, periodic swelling discomfort, facial asymmetry, and the H/O of surgery at the same region 5 years earlier. The patient had a right-sided Class Ⅲ Maxillectomy performed under General Anaesthesia. There were no immediate post-operative problems however, delayed issues occurred. Chondromyxoid fibroma is uncommon and has various sites, making diagnosis difficult and often exclusionary. However, it has a good prognosis with a recurrence rate of up to 80 % in curettage-only patients and a 2 % chance of malignant transformation. This example emphasizes the importance of a thorough clinical examination and histological comparison of CMFs with comparable lesions for optimal therapy. As shown in our case timely intervention can improve results and quality of life for affected cases.
口腔-面部软骨粘液样纤维瘤1例报告
软骨黏液样纤维瘤(CMF)是一种罕见的、生长缓慢的良性成软骨细胞肿瘤,伴有低细胞或软骨黏液样组织和多核细胞。与侵袭性肿瘤(如软骨肉瘤)相似的病理使CMFs更难识别。这种病变可能会引起疼痛的肿胀或扩大,持续数周或数年,也可能在放射扫描中偶然发现。一名24岁的女孩被诊断患有右上颌骨的CMF。她出现肿块发展,周期性肿胀不适,面部不对称,5年前同一区域手术的H/O。患者在全身麻醉下行右侧ClassⅢ上颌切除术。没有立即出现术后问题,但出现了延迟性问题。软骨粘液样纤维瘤是罕见的,有不同的部位,使诊断困难,往往排他性。然而,它具有良好的预后,在仅刮除的患者中复发率高达80% %,恶性转化的几率为2% %。这个例子强调了彻底的临床检查和CMFs与同类病变的组织学比较对于最佳治疗的重要性。正如我们的病例所示,及时干预可以改善受影响病例的结果和生活质量。
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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