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颞骨软骨黏液样纤维瘤:1例罕见病例报告

Chondromyxoid fibroma of the temporal bone: A rare case report.

作者信息

Liu Tao, Yao Jing, Li Xiaoyu, Qi Xinmeng, Zhao Pengyun, Tan Zhiqiao, Wang Jie, Li Yongxin

机构信息

Department of Otorhinolaryngology, Affiliated Hospital of Jining Medical University.

Department of Pharmacology, Jining Medical University, Jining.

出版信息

Medicine (Baltimore). 2020 Mar;99(11):e19487. doi: 10.1097/MD.0000000000019487.

Abstract

RATIONALE

Chondromyxoid fibroma (CMF) is a rare form of benign bone tumor and easily misdiagnosed as fibrosarcoma. Hence, to explore the clinical manifestations, diagnostic tests, and therapeutic procedures for temporal bone cartilage myxoid fibroma, it is important to optimize patient treatment and avoid overtreatment. Previous research has discussed cases of CMF, but this paper presents a systematic, complete, and comprehensive introduction of this disease based on this case and related literature.

PATIENT CONCERNS

A 52-year-old male patient presented with pain in his right ear for 2 years and hearing loss in his right ear with tinnitus for 1 year. The patient had a history of hypertension for 9 years and it was well-controlled.

DIAGNOSIS

A computed tomography (CT) scan of the temporal bone showed an expansive growth on the right temporal bone plate and tympanic plate, presenting as a cloud-like ground glass opaque shadow involving the temporom and ibular joint, middle skull base, and small auditory bones. A magnetic resonance imaging (MRI) of the temporal bone showed a large and irregular soft tissue mass shadow on the right temporal bone plate. The right temporal bone plate was occupied by the lesion, consistent with a bone origin. From the results of the imaging examination of the patient, a lesion occupying the temporal bone in the right ear and mastoiditis in the right middle ear was initially diagnosed.

INTERVENTIONS

Right ear temporal bone tumor resection and abdominal fat extraction were conducted.

OUTCOMES

Postoperative pathological results demonstrated myxoid fibroma of the temporal bone cartilage. No recurrence or severe complications were observed in 8 months of follow-up.

LESSONS

A finding of myxoid fibroma of the temporal bone cartilage is rare in the clinic. The growth of such tumors is slow. The temporal bone CT and inner ear MRI were helpful in diagnosis. Surgery was the principal treatment.

摘要

理论依据

软骨黏液样纤维瘤(CMF)是一种罕见的良性骨肿瘤,容易被误诊为纤维肉瘤。因此,为了探索颞骨软骨黏液样纤维瘤的临床表现、诊断测试和治疗方法,优化患者治疗并避免过度治疗非常重要。以往的研究已经讨论过CMF的病例,但本文基于该病例及相关文献对这种疾病进行了系统、完整和全面的介绍。

患者情况

一名52岁男性患者,右耳疼痛2年,右耳听力下降伴耳鸣1年。该患者有9年高血压病史,病情控制良好。

诊断

颞骨计算机断层扫描(CT)显示右侧颞骨板和鼓膜板呈膨胀性生长,表现为累及颞下颌关节、中颅底和小听骨的云雾状磨玻璃样不透明阴影。颞骨磁共振成像(MRI)显示右侧颞骨板有一个大的不规则软组织肿块阴影。右侧颞骨板被病变占据,符合骨源性。根据患者的影像学检查结果,初步诊断为右耳颞骨占位性病变和右中耳乳突炎。

干预措施

进行了右耳颞骨肿瘤切除术和腹部脂肪抽取术。

结果

术后病理结果显示为颞骨软骨黏液样纤维瘤。随访8个月未观察到复发或严重并发症。

经验教训

颞骨软骨黏液样纤维瘤在临床上很少见。此类肿瘤生长缓慢。颞骨CT和内耳MRI有助于诊断。手术是主要治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7de/7440231/562a9402c85d/medi-99-e19487-g001.jpg

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