Primary Chest Wall Glomus Tumor Resected by Video-Assisted Thoracoscopic Surgery: A Case Report with 10-Year Follow-up.

IF 0.7 Q4 SURGERY
Surgical Case Reports Pub Date : 2026-01-01 Epub Date: 2026-07-24 DOI:10.70352/scrj.cr.26-0226
Noritake Kikunishi, Tetsukan Woo, Daisuke Noma, Atsuko Osawa, Takashi Nakayama, Aya Saito
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引用次数: 0

Abstract

Introduction: Glomus tumors are rare perivascular neoplasms that typically occur in the distal extremities. Their occurrence in the chest wall is extremely rare, with only 13 cases previously reported in the English literature. Herein, we report a unique case of a primary chest wall glomus tumor in a patient who presented with severe, rapidly worsening back pain, underwent 18F-fluorodeoxyglucose-PET/CT (FDG-PET/CT) evaluation, and experienced complete pain resolution following thoracoscopic resection.

Case presentation: A 65-year-old man presented to our emergency department with a 1-month history of progressively worsening right posterior back pain. Contrast-enhanced CT revealed a 20 × 13-mm well-enhanced oval mass in the right posterior chest wall at the level of the ninth rib. MRI demonstrated heterogeneous intensity on T2-weighted images. FDG-PET/CT showed low tumor uptake with a maximum standardized uptake value (SUVmax) of 2.2. This finding was considered adjunctive metabolic information that did not strongly suggest a highly aggressive malignancy; however, it was insufficient to exclude malignancy or establish a definitive diagnosis. To achieve a definitive diagnosis and alleviate the severe pain, surgical resection was performed via 4-port video-assisted thoracoscopic surgery (VATS). The tumor was completely excised with clear margins. Histopathological and immunohistochemical analyses confirmed the diagnosis of a benign glomus tumor, with diffuse positivity for smooth muscle actin (SMA) and a Ki-67 labeling index of less than 1%. The patient's severe back pain completely resolved immediately after surgery, and he remained completely asymptomatic with no evidence of recurrence at the 10-year follow-up.

Conclusions: Although exceedingly rare, glomus tumors should be included in the differential diagnosis of painful chest wall tumors. FDG-PET/CT may provide adjunctive information regarding metabolic activity during preoperative assessment; however, its findings should be interpreted cautiously and cannot replace histopathological evaluation. To the best of our knowledge, this is the first reported case of a chest wall glomus tumor evaluated with FDG-PET/CT. Complete surgical resection remains essential for definitive diagnosis and symptom relief, and minimally invasive resection via VATS may be an effective approach when complete resection is feasible.

电视胸腔镜手术切除原发性胸壁血管球瘤1例,随访10年。
血管球瘤是一种罕见的血管周围肿瘤,通常发生在肢体远端。它们在胸壁的发生极为罕见,在英国文献中仅报道了13例。在此,我们报告一例独特的原发性胸壁血管球瘤患者,该患者表现为严重且迅速恶化的背部疼痛,接受了18f -氟氧葡萄糖- pet /CT (FDG-PET/CT)评估,并在胸腔镜切除后完全缓解了疼痛。病例介绍:一名65岁男性因右后背部疼痛1个月进行性恶化就诊于急诊科。增强CT示右侧后胸壁第9肋位一20 × 13毫米增强良好的椭圆形肿块。MRI显示t2加权图像强度不均。FDG-PET/CT显示肿瘤摄取低,最大标准化摄取值(SUVmax)为2.2。这一发现被认为是辅助代谢信息,不强烈提示高度侵袭性恶性肿瘤;然而,它不足以排除恶性肿瘤或建立一个明确的诊断。为了获得明确的诊断并减轻严重的疼痛,通过4端口视频辅助胸腔镜手术(VATS)进行手术切除。肿瘤完全切除,边缘清晰。组织病理学和免疫组织化学分析证实了良性血管球瘤的诊断,平滑肌肌动蛋白(SMA)弥漫阳性,Ki-67标记指数小于1%。患者的严重背部疼痛在手术后立即完全缓解,在10年随访中完全无症状,无复发迹象。结论:尽管极为罕见,但球囊瘤应列入胸壁疼痛性肿瘤的鉴别诊断。FDG-PET/CT可以在术前评估中提供有关代谢活动的辅助信息;然而,其结果应谨慎解释,不能取代组织病理学评价。据我们所知,这是第一例用FDG-PET/CT评估胸壁血管球瘤的病例。完全手术切除对于明确诊断和缓解症状仍然至关重要,当完全切除可行时,通过VATS进行微创切除可能是有效的方法。
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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