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Temporal bone central giant-cell granuloma presenting as a serous otitis media.

机译:颞骨中央巨细胞肉芽肿呈浆液性中耳炎。

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摘要

Central giant cell granuloma is a benign intraosseous lesion that most commonly occurs in the facial bones. Its location in the temporal bone is extremely rare and only 20 cases have been reported in the literature. We report a case of an adult female patient presenting with a right serous otitis media and mastoiditis associated with a mixed hearing loss during 6 months. CT-scan and MRI revealed a temporal bone tumor involving the mastoid, and surrounding the right temporo-mandibular joint. Tumor was totally removed after a canal-wall-down mastoidectomy and middle ear exclusion. Pathology revealed a central giant cell granuloma. Seven months following the surgery there was no evidence of recurrence. Central giant cell granuloma is a rare temporal bone lesion, with non specific clinical and imaging signs but characteristic pathological features. Today, a total surgical removal and regular MRI follow-up is the best management option.
机译:中枢巨细胞肉芽肿是一种良性骨内病变,最常见于面部骨骼。它在颞骨中的位置非常少见,文献中仅报道了20例。我们报告了一例成年女性患者,在6个月内出现右浆液性中耳炎和乳突炎,伴有混合性听力下降。 CT扫描和MRI显示颞骨肿瘤累及乳突,并围绕颞下颌关节。乳突管切除术和中耳排斥后,肿瘤被完全切除。病理显示有中央巨细胞肉芽肿。手术后七个月,没有复发的迹象。中枢巨细胞肉芽肿是一种罕见的颞骨病变,具有非特异性的临床和影像学征象,但具有病理特征。如今,完全手术切除和定期MRI随访是最好的治疗选择。

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