Surgical Management of a Giant Mediastinal Schwannoma Associated with Neurofibromatosis Type 1: A Case Report.

IF 0.7 Q4 SURGERY
Surgical Case Reports Pub Date : 2025-01-01 Epub Date: 2025-08-22 DOI:10.70352/scrj.cr.25-0150
Shin-Nosuke Watanabe, Daisuke Kimura, Kengo Tani, Takahiro Sasaki, Shuta Kimura, Chisaki Muto, Tsubasa Kato, Masahito Minakawa
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Abstract

Introduction: Neurogenic tumors commonly develop in the posterior mediastinum in both pediatric and adult patients. In patients with neurofibromatosis type 1, distinguishing benign schwannomas from malignant peripheral nerve sheath tumors is challenging. In this study, we aimed to present the surgical management of a giant schwannoma that required differentiation from a malignant peripheral nerve sheath tumor.

Case presentation: A 15-year-old boy presented with a large right mediastinal mass discovered on chest radiography at high school admission. Subsequent contrast-enhanced CT of the chest showed the development of a large tumor (16.0 × 12.5 × 11.8 cm) occupying approximately two-thirds of the right thoracic cavity, with atelectasis of the lower lobe of the right lung. The patient was histopathologically diagnosed with a benign schwannoma associated with neurofibromatosis type 1 through a thoracoscopic biopsy of the tumor and had received oral selumetinib at 50-70 mg/day for 11 months. Surgical excision was performed because of tumor progression and suspected malignant transformation. Right posterolateral thoracotomy with the opening of the 6th intercostal space was performed by extending the anterior skin incision along the abdominal rectus muscle and separating the 6th costal cartilage and diaphragmatic margin along the chest wall. The tumor was completely removed by resecting numerous adhesions between the tumor and the surrounding tissues and coagulating several nutrient vessels that flowed into the tumor, while resecting the lower lobe of the lung. The postoperative course was uneventful. The pathological examination revealed no malignancy. Subsequent contrast-enhanced CT of the chest revealed no residual tumors.

Conclusions: Posterolateral thoracotomy with the separation of the costal cartilage and diaphragmatic margin along the chest wall could achieve safe surgery for a giant mediastinal schwannoma.

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巨大纵隔神经鞘瘤合并1型神经纤维瘤病的外科治疗1例。
神经源性肿瘤通常发生在儿童和成人的后纵隔。在1型神经纤维瘤病患者中,区分良性神经鞘瘤和恶性周围神经鞘瘤是具有挑战性的。在这项研究中,我们的目的是提出一个需要从恶性周围神经鞘肿瘤分化的巨大神经鞘瘤的手术治疗。病例介绍:一名15岁的男孩在高中入学时胸部x线片上发现了一个大的右侧纵隔肿块。随后的胸部增强CT显示一个大肿瘤(16.0 × 12.5 × 11.8 cm),约占右胸腔的三分之二,右肺下叶不张。患者通过胸腔镜肿瘤活检被组织病理学诊断为良性神经鞘瘤伴1型神经纤维瘤病,并接受50- 70mg /天口服selumetinib治疗11个月。因肿瘤进展及疑似恶性转化,行手术切除。右后外侧开胸,沿腹直肌延伸前皮肤切口,沿胸壁分离第6肋软骨和膈缘,开第6肋间隙。通过切除肿瘤与周围组织之间的大量粘连,凝固流入肿瘤的几条营养血管,同时切除肺下叶,肿瘤被完全切除。术后过程平淡无奇。病理检查未见恶性肿瘤。胸部增强CT未见肿瘤残留。结论:沿胸壁后外侧开胸分离肋软骨和膈缘是治疗巨大纵隔神经鞘瘤的安全方法。
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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