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外耳道和颞骨血管瘤:病例报告及文献综述

Hemangioma of the External Auditory Canal and Temporal Bone: A Case Report and Comprehensive Literature Review.

机构信息

King Abdullah Ear Specialist Center (KAESC), College of Medicine, King Saud University Medical City (KSUMC), King Saud University, Riyadh, Saudi Arabia.

Ohud General Hospital, Ministry of Health, AL Medina, Kingdom of Saudi Arabia.

出版信息

Ear Nose Throat J. 2024 Dec;103(12):NP720-NP726. doi: 10.1177/01455613211029795. Epub 2022 Mar 31.

Abstract

Although hemangiomas are common in the head and neck area, they are uncommon in the temporal bone. External auditory canal (EAC) hemangiomas are a relatively uncommon otologic condition. In the English literature, only 29 cases of temporal bone hemangioma have been reported. We also present the case of a 32-year-old male patient who presented with an 8-month history of decreased hearing, tinnitus, and aural fullness on the right side. Otoscopic examination of the right ear revealed a smooth, oval, well-circumscribed, reddish, pulsatile, nontender mass, which was about 1 cm in diameter and occupied two-thirds of the EAC. It was soft in consistency, compressible, and appeared to be arising from the right posterior-superior portion of the bony canal wall; the tympanic membrane seemed to be uninvolved. The patient had mild conductive hearing loss of the right ear with an average air-bone gap of 20 dB; the left side was normal. High-resolution contrast-enhanced computed tomographic scanning of the temporal bone showed well-defined, rounded, homogenously enhancing lesions at the posterior-superior aspect of right EAC measuring 0.7 × 0.8 cm. Angiography was performed and there was evidence of vascular blush in the region of the right EAC. Three blood vessels were identified and embolized. The mass was completely removed by the endaural approach, and a retroauricular skin graft to restore cutaneous integrity was not required. Histopathology indicated a capillary hemangioma without cytological atypia or mitotic activity. There was no recurrence 1 year after the surgery.

摘要

尽管血管瘤在头颈部很常见,但在颞骨中却不常见。外耳道(EAC)血管瘤是一种相对罕见的耳科学疾病。在英文文献中,仅有 29 例颞骨血管瘤的报道。我们还报告了 1 例 32 岁男性患者,其右侧听力下降、耳鸣和耳闷 8 个月。右侧耳镜检查显示一个光滑、椭圆形、边界清楚、红色、搏动性、无触痛的肿块,直径约 1 厘米,占据 EAC 的三分之二。肿块质地柔软,可压缩,似乎起源于骨性耳道后壁的右上部分;鼓膜似乎未受累。患者右侧中度传导性听力损失,气骨导平均差值为 20 dB;左侧正常。颞骨高分辨率增强 CT 扫描显示右侧 EAC 后上象限边界清楚、呈圆形、均匀强化的病变,大小为 0.7×0.8 cm。进行了血管造影,右侧 EAC 区域可见血管染色。识别出 3 条血管并进行了栓塞。通过耳后入路完全切除了肿块,无需进行耳后皮肤移植以恢复皮肤完整性。组织病理学显示为毛细血管型血管瘤,无细胞学异型性或有丝分裂活动。手术后 1 年无复发。

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