Perkins Sidney J, Gao Rebecca, Glazer Tiffany A, Zhao Cher X, Basura Gregory, McKean Erin L
Medical School, University of Michigan Medical School, Ann Arbor, Michigan, United States.
Department of Otolaryngology-Head and Neck Surgery, University of Michigan, Ann Arbor, Michigan, United States.
J Neurol Surg B Skull Base. 2021 Sep 10;83(Suppl 2):e555-e563. doi: 10.1055/s-0041-1735558. eCollection 2022 Jun.
Inflammatory pseudotumor (IPT) of the skull base is a rare, locally destructive lesion managed with a variety of treatments. We explore the impact of treatment on outcome and assess the prognosis of IPT. This is a retrospective review of IPT of the skull base at a tertiary academic medical center. The primary outcome was radiographic progression after treatment. Outcome versus tumor location was also examined and a prognostic model was developed using a logistic regression. The demographics of 21 patients with IPT are reported. Treatment consisted of corticosteroids (in 80.1% of patients), disease modifying antirheumatic drugs (DMARDs; 33.3%), surgical resection (28.6%), radiation (23.8%), antibiotics (14.3%), chemotherapy (rituximab; 9.5%), and antivirals (4.8%). At 50.7 months, 50.8% had radiographic progression. Local therapy trended toward having a better response than systemic therapy ( = 0.60). IPT of the orbit required 2.4 treatment modalities, compared with 2.0 for pharyngeal IPT, and 1.3 for posterior skull base masses ( = 0.14). A total of 75% orbital IPT underwent radiographic progression, compared with 71% of pharyngeal IPT and 50% of posterior skull base masses ( = 0.62). Sixteen patients were used to create the logistic model of radiographic progression. The Cox-Snell was 0.71 ( = 0.03). No individual variables were statistically significant. To our knowledge, this is among the largest sample of cases describing the presentation, treatment, and prognosis of IPT of the skull base. Our data suggest that there may be an improved response with local therapy over systemic therapy and better prognosis among posterolateral skull base masses.
颅底炎性假瘤(IPT)是一种罕见的、具有局部破坏性的病变,可采用多种治疗方法。我们探讨了治疗对预后的影响,并评估了IPT的预后。 这是对一家三级学术医学中心颅底IPT的回顾性研究。主要结局是治疗后的影像学进展。还研究了结局与肿瘤位置的关系,并使用逻辑回归建立了预后模型。 报告了21例IPT患者的人口统计学数据。治疗方法包括使用皮质类固醇(80.1%的患者)、改善病情抗风湿药(DMARDs;33.3%)、手术切除(28.6%)、放疗(23.8%)、抗生素(14.3%)、化疗(利妥昔单抗;9.5%)和抗病毒药物(4.8%)。在50.7个月时,50.8%的患者出现影像学进展。局部治疗的反应趋势优于全身治疗(P = 0.60)。眼眶IPT需要2.4种治疗方式,相比之下,咽IPT为2.0种,后颅底肿块为1.3种(P = 0.14)。眼眶IPT共有75%出现影像学进展,咽IPT为71%,后颅底肿块为50%(P = 0.62)。16例患者用于建立影像学进展的逻辑模型。Cox-Snell R²为0.71(P = 0.03)。没有单个变量具有统计学意义。 据我们所知,这是描述颅底IPT的表现、治疗和预后的最大病例样本之一。我们的数据表明,局部治疗可能比全身治疗反应更好,后外侧颅底肿块的预后更佳。