Baker Austin T, Homewood Tyler J, Baker Terry R
Texas College of Osteopathic Medicine, University of North Texas Health Science Center, 3500 Camp Bowie Blvd., Fort Worth, TX, 76107, USA.
Mountain View Hospital 2325 Coronado St, Idaho Falls, ID 83404, USA; Idaho Falls ENT, 3200 Channing Way Ste A105, Idaho Falls, ID 83404, USA.
Int J Surg Case Rep. 2018;49:4-7. doi: 10.1016/j.ijscr.2018.06.001. Epub 2018 Jun 9.
Cervical Sympathetic Chain Schwannomas (CSCS) of the carotid sheath are rare neoplasms that can be misdiagnosed on imaging. The following case documents a rare incident of a misdiagnosed CSCS with unusual outcomes of permanent Horner's syndrome and facial pain.
A 36-year-old female presented with a slow-growing neck mass. CT and MRI led to a preoperative diagnosis of vagus nerve schwannoma (VNS). However, surgical treatment revealed the mass to be involved with the cervical sympathetic chain rather than the vagus nerve. The diagnosis was corrected to CSCS and the nerve was resected with the mass. The patient presented postoperatively with Horner's syndrome and severe facial pain. These symptoms persisted despite two years of medical management.
Studies indicate that imaging trends used for distinction between VNS and CSCS show inconsistencies in making preoperative diagnoses. Recent literature reveals helpful criteria for improving diagnostic standards that assist with preoperative patient counseling. In addition, postoperative outcomes, such as temporary, asymptomatic Horner's syndrome are common in CSCS. The following case report exemplifies the difficulties in diagnosis and addresses the unique complications of facial pain and permanent Horner's syndrome.
This case report examines postoperative outcomes and improves clinician awareness of the potential for misdiagnosis of a rare neoplasm and the recently improved diagnostic measures, providing for higher quality preoperative counseling. Future research is recommended to confirm and improve diagnostic guidelines and accuracy. Additional studies may focus on evaluating the effects of incorrect preoperative diagnosis on postoperative complication rates.
颈动脉鞘区的颈交感神经链神经鞘瘤(CSCS)是一种罕见的肿瘤,在影像学上可能会被误诊。以下病例记录了一例罕见的误诊CSCS事件,伴有永久性霍纳综合征和面部疼痛等异常结果。
一名36岁女性因颈部肿块生长缓慢前来就诊。CT和MRI检查术前诊断为迷走神经鞘瘤(VNS)。然而,手术治疗发现肿块与颈交感神经链有关,而非迷走神经。诊断更正为CSCS,并将神经与肿块一并切除。患者术后出现霍纳综合征和严重的面部疼痛。尽管经过两年的药物治疗,这些症状仍然存在。
研究表明,用于区分VNS和CSCS的影像学趋势在术前诊断中存在不一致性。最近的文献揭示了有助于提高诊断标准的有用标准,有助于术前对患者进行咨询。此外,术后结果,如暂时性无症状霍纳综合征在CSCS中很常见。以下病例报告举例说明了诊断的困难,并探讨了面部疼痛和永久性霍纳综合征的独特并发症。
本病例报告研究了术后结果,提高了临床医生对罕见肿瘤误诊可能性和最近改进的诊断措施的认识,为更高质量的术前咨询提供了依据。建议未来的研究确认并改进诊断指南和准确性。其他研究可能侧重于评估术前错误诊断对术后并发症发生率的影响。