Brown Hannah G, Torres Bryan S, Nuñez Julisa, Wong Richard J, Hajjar Fouad M, Abongwa Chenue, Sawh-Martinez Rajendra F, Lopez Joseph
From University of Central Florida, College of Medicine, Orlando, Fla.
Tulane University, School of Medicine, New Orleans, La.
Plast Reconstr Surg Glob Open. 2024 May 22;12(5):e5763. doi: 10.1097/GOX.0000000000005763. eCollection 2024 May.
A 13-year-old girl with a painful left neck mass was referred to our institution due to suspicions of malignancy. The patient reported pain that accompanied her frequent neck spasms. Computed tomography revealed a large, soft-tissue mass in the left neck, deep to the sternocleidomastoid. The lesion anteriorly displaced the internal carotid artery and both displaced and crushed the internal left jugular vein. Uniquely, a three-dimensional virtual reality model combining magnetic resonance imaging and computed tomography data was used to determine the lesion's resectability and visualize which structures would be encountered or require protection while ensuring total resection. During operation, we confirmed that the mass also laterally displaced the brachial plexus, cranial nerves X and XI, and spinal nerves C3-C5 (including the phrenic) of the cervical plexus. Postsurgical pathological analysis confirmed a diagnosis of desmoid tumor, also known as aggressive fibromatosis, whereas DNA sequencing revealed a mutation, a somatic genetic marker found in approximately 90% of desmoid tumor cases. When possible, the most widely used method for the treatment of desmoid tumors has been gross resection. Chemotherapy, radiotherapy, and local excision are also used in the treatment of fibromatoses when complete resection is judged infeasible. In this case, a complete surgical resection with tumor-free surgical margins was performed. A standard cervical approach with a modified posterolateral incision site was implemented to avoid a conspicuous anterior neck scar. No flap, nerve repair, or reconstruction was warranted. At 1 year of postsurgical follow-up, the patient showed minimal scarring and no signs of recurrence.
一名13岁左侧颈部肿物伴疼痛的女孩因怀疑恶性肿瘤被转诊至我院。患者自述疼痛伴有频繁的颈部痉挛。计算机断层扫描显示左侧颈部胸锁乳突肌深面有一个巨大的软组织肿物。该病变使颈内动脉向前移位,并使左侧颈内静脉移位并受压。独特的是,利用磁共振成像和计算机断层扫描数据相结合的三维虚拟现实模型来确定病变的可切除性,并可视化在确保完全切除的同时会遇到哪些结构或需要保护哪些结构。手术中,我们证实该肿物还使臂丛神经、迷走神经和副神经以及颈丛的颈3 - 颈5脊神经(包括膈神经)向外移位。术后病理分析确诊为硬纤维瘤,也称为侵袭性纤维瘤病,而DNA测序显示存在一种突变,这是在大约90%的硬纤维瘤病例中发现的一种体细胞遗传标记。在可能的情况下,治疗硬纤维瘤最常用的方法是根治性切除。当判断无法完全切除时,化疗、放疗和局部切除也用于纤维瘤病的治疗。在本病例中,进行了切缘无肿瘤的完整手术切除。采用标准的颈部入路并改良后外侧切口部位,以避免颈部前方明显的瘢痕。无需进行皮瓣、神经修复或重建。术后1年随访时,患者瘢痕轻微,无复发迹象。