Resected intramuscular hemangioma in the chest wall: a case report.

IF 0.7 Q4 SURGERY Surgical Case Reports Pub Date : 2024-09-26 DOI:10.1186/s40792-024-02023-4
Yoshiyuki Nakanishi, Takaki Akamine, Fumihiko Kinoshita, Mikihiro Kohno, Keigo Ozono, Takuya Hino, Taro Mori, Yoshinao Oda, Tomoyoshi Takenaka, Masafumi Nakamura
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Abstract

Background: Intramuscular hemangioma is an uncommon benign tumor found mainly in the limbs of adolescents and young adults. The local recurrence rate is high, ranging from 30 to 50%, necessitating wide local excision of intercostal intramuscular hemangiomas. However, preoperative diagnosis of intramuscular hemangiomas is challenging. Herein, we report a rare case of an intramuscular hemangioma arising from the chest wall.

Case presentation: A healthy 29-year-old asymptomatic man was referred to our hospital after an abnormal shadow was observed on his chest radiography. Computed tomography and magnetic resonance imaging revealed a 30-mm-sized mass in the right second intercostal space. Neoplastic lesions, such as schwannomas or solitary fibrous tumors, were included in the preoperative differential diagnosis. Tumor resection was performed using video-assisted thoracoscopic surgery. The tumor, which had a smooth surface covered with parietal pleura, was dissected from the external intercostal muscle and costal bone. Postoperative histopathological examination revealed proliferation of spindle-shaped endothelial cells arranged in a capillary vascular structure accompanied by entrapped smooth muscle fibers, adipose tissue, and muscle vessels. The final diagnosis was an intramuscular hemangioma with negative surgical margins. There was no evidence of recurrence during the 1-year postoperative follow-up period.

Conclusion: Intramuscular hemangiomas should be considered in the differential diagnosis of chest wall tumors, particularly in young people, owing to their potential for recurrence. Moreover, postoperative follow-up may be necessary for resected intramuscular intercostal hemangiomas.

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胸壁肌肉内血管瘤切除术:病例报告。
背景:肌内血管瘤是一种不常见的良性肿瘤,主要发生在青少年和年轻人的四肢。局部复发率很高,从 30% 到 50% 不等,因此有必要对肋间肌内血管瘤进行广泛的局部切除。然而,肌间血管瘤的术前诊断具有挑战性。在此,我们报告了一例罕见的胸壁肌内血管瘤病例:一名 29 岁无症状的健康男性因胸片发现异常阴影而被转诊至我院。计算机断层扫描和磁共振成像显示,右侧第二肋间隙有一个 30 毫米大小的肿块。术前鉴别诊断包括肿瘤病变,如分裂瘤或单发纤维瘤。采用视频辅助胸腔镜手术进行了肿瘤切除。肿瘤表面光滑,覆盖顶胸膜,从肋间外肌和肋骨上切除。术后组织病理学检查显示,呈纺锤形的内皮细胞增生,排列成毛细血管结构,并伴有夹杂的平滑肌纤维、脂肪组织和肌肉血管。最终诊断为肌肉内血管瘤,手术切缘阴性。术后 1 年的随访期间没有发现复发迹象:结论:由于肌内血管瘤有复发的可能性,因此在胸壁肿瘤的鉴别诊断中应考虑肌内血管瘤,尤其是年轻人。此外,切除的肋间肌内血管瘤可能需要术后随访。
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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