Large Skull Metastasis in Follicular Thyroid Carcinoma: A Comprehensive Case Presentation and Systematic Review

IF 0.9 4区 医学 Q4 CLINICAL NEUROLOGY Journal of neurological surgery. Part A, Central European neurosurgery Pub Date : 2024-04-15 DOI:10.1055/s-0044-1785650
Gianluca Scalia, Massimiliano Porzio, Roberta Costanzo, Eliana Giurato, Fabio Gibilisco, Domenico Gerardo Iacopino, Rosario Maugeri, Giovanni Federico Nicoletti, Giuseppe Emmanuele Umana, Raffaele Alessandrello
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Abstract

Background Skull metastases from follicular thyroid carcinoma (FTC) are infrequent but clinically significant, often presenting with localized pain, neurologic deficits, and cranial nerve dysfunction. Early detection and accurate diagnosis pose challenges due to their asymptomatic nature in some cases.

Methods A systematic literature review, conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, identified and analyzed 15 relevant studies focusing on large skull metastases in FTC. Data extraction and synthesis included clinical presentation, diagnostic methods, treatment strategies, and patient outcomes.

Results The systematic review encompassed 20 patients with secondary skull metastases from FTC, offering insights into the clinical diversity of this rare condition. Clinical presentations varied, with localized pain (70% of cases) and headaches being predominant symptoms. Imaging techniques, including computed tomography (CT) and magnetic resonance imaging (MRI), played a pivotal role in diagnosis. Surgical resection was considered in select cases, achieving complete or near-complete tumor removal in 30 to 50% of patients. Radiotherapy, including external beam radiation therapy (EBRT) and stereotactic radiosurgery (SRS), provided local control and symptom relief in 70 to 80% of cases. Systemic therapies, such as tyrosine kinase inhibitors (TKIs), showed promise in disease stabilization or regression (45% of patients). Prognosis remained poor, with a median overall survival of 6 to 12 months, reflecting an advanced and aggressive disease state.

Conclusion Managing secondary skull metastases from FTC requires a comprehensive approach, including surgical intervention, radiotherapy, and potential systemic therapies. The rarity of these metastases underscores the need for further research to establish standardized treatment guidelines, explore molecular profiling, and investigate immunotherapy and combination therapies, offering hope for improved outcomes in this challenging clinical scenario.

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滤泡性甲状腺癌的大块头骨转移:综合病例展示与系统综述
背景 滤泡性甲状腺癌(FTC)的颅骨转移并不常见,但临床意义重大,通常表现为局部疼痛、神经功能缺损和颅神经功能障碍。由于部分病例无症状,因此早期发现和准确诊断面临挑战。方法 根据《系统综述和荟萃分析首选报告项目》(Preferred Reporting Items for Systematic Reviews and Meta-Analyses,PRISMA)指南进行了系统文献综述,确定并分析了 15 项相关研究,重点关注 FTC 中的大颅骨转移瘤。数据提取和综合包括临床表现、诊断方法、治疗策略和患者预后。结果 该系统综述涵盖了20例FTC继发性颅骨转移瘤患者,使人们对这种罕见疾病的临床多样性有了更深入的了解。临床表现各不相同,局部疼痛(70% 的病例)和头痛是主要症状。包括计算机断层扫描(CT)和磁共振成像(MRI)在内的成像技术在诊断中发挥了关键作用。对部分病例考虑进行手术切除,30%至50%的患者可实现肿瘤完全或接近完全切除。放疗,包括体外放射治疗(EBRT)和立体定向放射外科治疗(SRS),在70%至80%的病例中可达到局部控制和缓解症状的效果。酪氨酸激酶抑制剂(TKIs)等全身疗法有望使病情稳定或缓解(45%的患者)。预后仍然不佳,中位总生存期为 6 至 12 个月,反映了疾病的晚期和侵袭性。结论 治疗 FTC 继发性颅骨转移需要采取综合方法,包括手术干预、放疗和潜在的全身疗法。这些转移瘤的罕见性凸显了进一步研究的必要性,以建立标准化的治疗指南、探索分子图谱、研究免疫疗法和联合疗法,为改善这种具有挑战性的临床情况的预后带来希望。
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来源期刊
CiteScore
2.30
自引率
0.00%
发文量
90
期刊介绍: The Journal of Neurological Surgery Part A: Central European Neurosurgery (JNLS A) is a major publication from the world''s leading publisher in neurosurgery. JNLS A currently serves as the official organ of several national neurosurgery societies. JNLS A is a peer-reviewed journal publishing original research, review articles, and technical notes covering all aspects of neurological surgery. The focus of JNLS A includes microsurgery as well as the latest minimally invasive techniques, such as stereotactic-guided surgery, endoscopy, and endovascular procedures. JNLS A covers purely neurosurgical topics.
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