Sente Marko
Srp Arh Celok Lek. 2009 Jan-Feb;137(1-2):73-6. doi: 10.2298/sarh0902073s.
Osteomas are a slow growing benign neoplasm of unknown etiology very rarely involving the temporal bone. They develop in the external auditory canal on squamous sections, in the mastoid, middle and inner ear. By bone composition they are divided into spongious (osteoma spongiosum) and compact osteomas (osteoma eburnum); by growth direction, into outward-growing (exosteoma) and in inward-growing (endosteoma); into unilateral and bilateral; by size, into small and gigantic; by surface structure, into smooth and multilobular; by number, into solitary and multiple; into symmetrical and asymmetrical. The symptoms of intracanalicular osteomas are the result of auditory canal obstruction. Diagnosis is made based on case history, clinical examination, audiological processing and radiography (temporal bone CT scan), and confirmed by histopathological examination of the bone. In terms of differential diagnosis, they must be distinguished from exostoses, bone tissue proliferation and osteoid osteomata. The progress of the disease is prolonged, as they are slow growing, asymptomatic and benign tumours. Therapy is surgical only.
The report presents the case of a 70-year old patient with the osteoma of the right external auditory canal. In our patient, the osteoma arose in the auditory canal, the most frequent localization; it was unilateral, solitary, multilobular and compact. It was discovered accidentally, during otoscopic examination. The clinical diagnosis was confirmed by CT scan of the temporal bone. We applied surgical therapy by retroauricular approach. The removed bone change was about 12 mm high, 13-14 mm deep and about 8 mm wide. Histopathological findings confirmed osteoma.
Due to their slow growth, the rate of auditory canal osteomas develop asymptomatically for a long time without the characteristic clinical features. In most cases, they are discovered accidentally during otoscopic or radiographic examination. The method of choice in diagnosis is temporal bone CT scan. Therapy is surgical.
骨瘤是一种生长缓慢的良性肿瘤,病因不明,很少累及颞骨。它们发生于外耳道的鳞状上皮部位、乳突、中耳和内耳。根据骨质成分,可分为海绵状骨瘤(osteoma spongiosum)和致密骨瘤(osteoma eburnum);根据生长方向,可分为向外生长型(外生骨瘤)和向内生长型(内生骨瘤);根据单侧或双侧;根据大小,可分为小型和巨型;根据表面结构,可分为光滑型和多叶型;根据数量,可分为单发和多发;根据对称性,可分为对称型和不对称型。管内型骨瘤的症状是耳道阻塞的结果。诊断基于病史、临床检查、听力学检查和影像学检查(颞骨CT扫描),并通过骨组织病理检查确诊。在鉴别诊断方面,必须将其与外耳道骨疣、骨组织增生和骨样骨瘤相区分。由于它们是生长缓慢、无症状的良性肿瘤,疾病进展缓慢。治疗仅采用手术方式。
本报告介绍了一名70岁患有右外耳道骨瘤患者的病例。在我们的患者中,骨瘤发生于耳道,这是最常见的部位;为单侧、单发、多叶型且为致密型。它是在耳镜检查时偶然发现的。颞骨CT扫描证实了临床诊断。我们采用耳后入路进行手术治疗。切除的骨质病变高约12毫米,深13 - 14毫米,宽约8毫米。组织病理学检查结果证实为骨瘤。
由于生长缓慢,耳道骨瘤在很长一段时间内无症状发展,没有特征性临床症状。大多数情况下,它们是在耳镜检查或影像学检查时偶然发现的。诊断的首选方法是颞骨CT扫描。治疗采用手术方式。