Clinical and neuroradiological red flags in differential diagnosis of pituitary metastases and PitNETs (adenomas): a surgeon's experience and systematic literature review.
Riccardo Antonio Ricciuti, Riccardo Paracino, Fabrizio Mancini, Pierfrancesco De Domenico, Vittorio Ricciuti, Francesca Romana Barbieri, Matteo Maria Ottaviani, Serena Pagano, Daniele Marruzzo
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引用次数: 0
Abstract
Introduction: Pituitary metastases (PMs) are rare malignancy manifestations, generally deemed to have an extremely poor prognosis. Differential diagnosis from primary pituitary lesions is often difficult, as their features can mimic those of pituitary neuroendocrine tumours (PitNETs). This study aimed to report a single surgeon's experience in managing PMs and to gather the existing evidence on their clinical and neuroradiological presentation to build a model of 'red flags' that help raise the suspicion of PMs in the context of sellar lesions.
Material and methods: We retrieved an original 10-year surgical series of patients undergoing endoscopic transsphenoidal (TNS) surgery for suspected PitNETs, and we additionally conducted a systematic review of case reports or series of patients with PMs.
Results: The local series consisted of n = 6 PMs. The literature review yielded n = 149 works reporting n = 340 PMs. Overall, the clinical presentation and neuroradiological features of n = 346 PMs were analysed and compared to data retrieved from n = 361 PitNETs from our original cohort. Primary features associated with PMs were: the presence of headaches (OR 1.24, p = 0.001), visual field deficits (OR 1.19, p = 0.02), extraocular nerve palsies (OR 1.23, p = 0.001), diabetes insipidus (OR 2.13, p < 0.001), MRI features of pituitary stalk/infundibular involvement (OR 1.98, p = 0.001), cavernous sinus invasion (OR 1.57, p = 0.004), and T2w flow voids (OR 1.13, p = 0.001). An incidental diagnosis (OR 0.49, p < 0.001) and cystic changes (OR 0.77, p = 0.02) were less common among PMs. Secondary features involved an acute onset of symptoms (OR 1.25, p = 0.001), the presence of oncological history (OR 1.89, p = 0.001), sellar walls erosion (OR 1.55, p = 0.002), and gross appearance of a firm (OR 2.01, p < 0.001) and easily bleeding lesion (OR 1.99, p < 0.001). Sellar enlargement predicted a lower risk of PMs (OR 0.54, p = 0.001).
Conclusion: We have compiled a list of primary and secondary red flags, including clinical and neuroradiological features, to serve as a guiding tool for clinicians to raise suspicion of PMs and aid in the differential diagnosis of various lesions centered in the sella.
垂体转移瘤是一种罕见的恶性肿瘤,通常被认为预后极差。原发性垂体病变的鉴别诊断通常是困难的,因为它们的特征与垂体神经内分泌肿瘤(PitNETs)相似。本研究旨在报告一名外科医生在治疗经颅综合征方面的经验,并收集有关其临床和神经放射学表现的现有证据,以建立一个“危险信号”模型,帮助提高对鞍区病变背景下经颅综合征的怀疑。材料和方法:我们检索了最初10年的手术系列患者,他们接受了内镜下经蝶窦(TNS)手术治疗疑似PitNETs,我们还对pm患者的病例报告或系列患者进行了系统回顾。结果:局部序列包括n = 6个pm。文献综述共获得n = 149篇文献报道n = 340例pm。总体而言,我们分析了n = 346例pm的临床表现和神经放射学特征,并将其与原始队列中n = 361例PitNETs的数据进行了比较。与pm相关的主要特征是:头痛(OR 1.24, p = 0.001)、视野缺损(OR 1.19, p = 0.02)、眼外神经麻痹(OR 1.23, p = 0.001)、尿崩症(OR 2.13, p < 0.001)、垂体柄/小叶受累的MRI特征(OR 1.98, p = 0.001)、海绵窦侵犯(OR 1.57, p = 0.004)和T2w流腔(OR 1.13, p = 0.001)。意外诊断(OR 0.49, p < 0.001)和囊性改变(OR 0.77, p = 0.02)在pm中较少见。次要特征包括急性发作症状(OR 1.25, p = 0.001),存在肿瘤病史(OR 1.89, p = 0.001),鞍壁糜烂(OR 1.55, p = 0.002),大体表现为硬瘤(OR 2.01, p < 0.001)和易出血病变(OR 1.99, p < 0.001)。甲状腺肿大预示较低的pm风险(OR 0.54, p = 0.001)。结论:我们编制了一份原发性和继发性危险信号清单,包括临床和神经放射学特征,作为临床医生提高pmms的怀疑和帮助鉴别诊断以鞍为中心的各种病变的指导工具。
期刊介绍:
Polish Journal of Neurology and Neurosurgery is an official journal of the Polish Society of Neurology and the Polish Society of Neurosurgeons, aimed at publishing high quality articles within the field of clinical neurology and neurosurgery, as well as related subspecialties. For more than a century, the journal has been providing its authors and readers with the opportunity to report, discuss, and share the issues important for every-day practice and research advances in the fields related to neurology and neurosurgery.