Primary glomangioma of the chest wall: case report and review of literature.

IF 0.4 Q4 SURGERY
Journal of Surgical Case Reports Pub Date : 2025-05-12 eCollection Date: 2025-05-01 DOI:10.1093/jscr/rjaf300
Zymantas Jagelavicius, Eitvile Mickeviciute, Edvardas Zurauskas, Ricardas Janilionis
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引用次数: 0

Abstract

Glomus tumors are rare neoplasms that usually appear in subungual locations. A primary glomus tumor in the chest wall is extremely rare. We present a case of a 42-year-old male with intermittent pain under the right scapula for approximately a year. No skin lesions were observed. A magnetic resonance imaging and computed tomography scan showed a well-defined subpleural lesion on the right side of the chest along the ninth intercostal space. The tumor was removed via video-assisted thoracic surgery. The pathological report revealed a glomangioma. We analyzed in detail existing cases of glomus tumors in the chest wall. The chest wall is a possible site of a glomus tumor, which doesn't have any specific clinical or radiological signs. Radical surgical removal should be the treatment of choice.

原发性胸壁血管瘤:1例报告及文献复习。
血管球瘤是一种罕见的肿瘤,通常出现在脚下部位。原发性胸壁血管球瘤极为罕见。我们提出一个42岁的男性病例,右肩胛骨下间歇性疼痛约一年。未见皮肤损伤。磁共振成像和计算机断层扫描显示胸部右侧沿第9肋间隙有明确的胸膜下病变。通过视频辅助胸外科手术切除肿瘤。病理报告显示为血管瘤。我们详细分析了现有的胸壁血管球瘤病例。胸壁可能是血管球瘤的一个部位,它没有任何特定的临床或放射学征象。根治性手术切除是治疗的首选。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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