Single-stage concomitant extended thymectomy for myasthenia gravis and enucleation of a left recurrent laryngeal nerve schwannoma via median sternotomy.

IF 0.4
Go Kamimura, Koki Maeda, Masaya Aoki, Satomi Imamura, Shoichiro Morizono, Yuto Nonaka, Aya Takeda, Toshiyuki Nagata, Kazuhiro Ueda
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引用次数: 0

Abstract

BACKGROUND: Myasthenia gravis (MG) without thymoma is often treated with extended thymectomy to improve symptom control and reduce immunotherapy requirements. Schwannoma of the recurrent laryngeal nerve (RLN) is rare, and surgical resection is usually curative. However, operative manipulation carries a risk of temporary or permanent vocal fold paralysis. When these conditions coexist, choosing staged versus single-stage surgery is non-trivial. A synchronous operation can consolidate perioperative care and recovery but demands careful planning to prevent respiratory complications, particularly if RLN palsy or myasthenic crisis occur. CASE PRESENTATION: A 65-year-old woman with generalized, thymoma-negative MG (acetylcholine-receptor antibody positive) had no hoarseness or dysphagia. Flexible laryngoscopy confirmed mobile vocal folds bilaterally. Chest radiography showed mediastinal widening without diaphragmatic paralysis. Contrast-enhanced CT and MRI revealed a right anterior mediastinal cystic lesion and a solid mass in the left tracheoesophageal groove abutting the RLN. ^18F-fluorodeoxyglucose positron emission tomography demonstrated uptake in the solid lesion (SUV_max 4.89). Transesophageal endoscopic ultrasound–guided fine-needle aspiration yielded spindle cells compatible with schwannoma, and the mass was considered RLN-derived. A single-stage median sternotomy was undertaken. Extended thymectomy was performed with bilateral phrenic exposure and en bloc removal of thymic/perithymic fat, followed by nerve-sparing enucleation of the left RLN tumor through a longitudinal epineurial window and meticulous intracapsular dissection, preserving macroscopic neural continuity. The postoperative intensive care unit course was uneventful: no dyspnea or dysphagia, normal voice, and laryngoscopy confirmed intact vocal fold mobility. A chest radiograph on postoperative day 5 was unremarkable, and the patient was discharged on day 7. Histopathology showed alternating Antoni A/B areas with virtually no mitoses; tumor cells were strongly S-100–positive, confirming schwannoma. CONCLUSIONS: In carefully selected patients with stable MG and no preoperative vocal fold dysfunction, single-stage median sternotomy enables safe concomitant extended thymectomy and RLN schwannoma enucleation. Success hinges on nerve-sparing technique and proactive perioperative planning for airway protection and potential MG crisis.

一期合并扩大胸腺切除术治疗重症肌无力及经胸骨正中切开术切除左喉返神经鞘瘤。
背景:无胸腺瘤的重症肌无力(MG)通常采用扩展胸腺切除术来治疗,以改善症状控制并减少免疫治疗需求。喉返神经鞘瘤是罕见的,手术切除通常是治愈的。然而,手术操作有暂时或永久性声带麻痹的风险。当这些条件并存时,选择分阶段手术还是单阶段手术是很重要的。同步手术可以巩固围手术期护理和恢复,但需要仔细规划防止呼吸并发症,特别是如果发生RLN麻痹或肌无力危象。病例介绍:一名65岁女性,全身胸腺瘤阴性MG(乙酰胆碱受体抗体阳性),无声音嘶哑或吞咽困难。软性喉镜检查证实双侧声带活动。胸片显示纵隔增宽,无膈肌麻痹。增强CT和MRI显示右侧前纵隔囊性病变和左侧气管食管沟靠近RLN的实性肿块。^ 18f -氟脱氧葡萄糖正电子发射断层扫描显示在实体病变中摄取(SUV_max 4.89)。经食管内镜超声引导下的细针穿刺获得与神经鞘瘤相容的梭形细胞,肿块被认为是rnn来源的。进行单期正中胸骨切开术。扩大胸腺切除术,双侧膈暴露,整体去除胸腺/胸腺周围脂肪,然后通过纵向神经外窗对左侧RLN肿瘤进行保留神经的去核,并进行细致的囊内剥离,保持宏观神经连续性。术后重症监护病房疗程顺利:无呼吸困难或吞咽困难,声音正常,喉镜检查证实声带活动完整。术后第5天胸片无明显异常,患者于第7天出院。组织病理学显示Antoni A/B区交替,几乎没有有丝分裂;肿瘤细胞s -100强烈阳性,证实神经鞘瘤。结论:在精心挑选的MG稳定且术前无声带功能障碍的患者中,单期胸骨正中切开术可以安全的同时行胸腺扩大切除术和RLN神经鞘瘤去核。成功取决于神经保留技术和积极的围手术期计划气道保护和潜在的MG危机。
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