Alahmari Mohammed S, Alshahrani Abdulaziz M, Alharbi Salmah M, Alzahrani Mohammed S, Asiry Ali, Alghamdi Waleed, Al-Ahmari Mohammad, Alzarei Ali
Otolaryngology-Head and Neck Surgery, Aseer Central Hospital, Abha, SAU.
Otolaryngology-Head and Neck Surgery, Armed Forces Hospital Southern Region, Khamis Mushait, SAU.
Cureus. 2024 Jul 10;16(7):e64223. doi: 10.7759/cureus.64223. eCollection 2024 Jul.
Osteochondromyxoma (OMX) is an extremely rare bone tumor and has been classified by the World Health Organization as a benign chondrogenic bone tumor. The tumor can be associated with Carney complex which is a rare autosomal dominant syndrome. The clinical presentation of the patient depends primarily on the location and the size of the tumor. It has an excellent prognosis with complete surgical excision. Here, in this case, we present a young female patient diagnosed with OMX without carney complex and underwent complete endoscopic surgical excision.
骨软骨黏液瘤（OMX）是一种极其罕见的骨肿瘤，世界卫生组织将其归类为良性软骨源性骨肿瘤。该肿瘤可能与卡尼综合征相关，卡尼综合征是一种罕见的常染色体显性综合征。患者的临床表现主要取决于肿瘤的位置和大小。通过完整的手术切除，其预后良好。在此，我们报告一例诊断为无卡尼综合征的骨软骨黏液瘤的年轻女性患者，并对其进行了完整的内镜手术切除。
