Alahmari Mohammed, Alkherayf Fahad, Lasso Andrea, Banaz Fatmahalzahra, Mohajeri Sepideh, Masoudian Pourya, Lamothe Andre, Agbi Charles, Caulley Lisa, Alshardan Mohammad, Kilty Shaun
Department of Otolaryngology-Head and Neck Surgery, University of Ottawa, Ottawa, Ontario, Canada.
Division of Neurosurgery, Department of Surgery, University of Ottawa, Ottawa, Ontario, Canada.
J Neurol Surg B Skull Base. 2021 Jan 21;83(Suppl 2):e1-e6. doi: 10.1055/s-0040-1722668. eCollection 2022 Jun.
Pituitary apoplexy (PA) is a rare complication of pituitary tumors that can present with a myriad of symptoms, including sudden onset cranial nerve deficits. After patient stabilization and hormone replacement, surgical decompression is often recommended. The timing of surgical decompression remains controversial. In this case series, we describe our institutional experience pertaining to the cranial nerve recovery in patients who underwent endoscopic endonasal transsphenoidal (EETS) surgery for PA while evaluating outcome based on tumor stage using the suprasellar infrasellar parasellar anterior posterior (SIPAP) classification. Present study is a single-institution retrospective cohort. A retrospective review of all EETS cases for pituitary tumor resection between November 2009 and August 2018. Queries of the hospital database were completed by trained personnel to identify cases of PA treated using the EETS approach. Baseline characteristics, tumor type, endocrine data, and SIPAP classification based on preoperative magnetic resonance imaging (MRI) and operation characteristics were extracted from medical records. Postoperative results were extracted for the duration of the follow-up period available for each patient. Fifteen cases of PA were identified. Patient follow-up period was a mean of 30 months. The cranial nerve deficits present at admission were visual deficit (33%); unilateral third nerve palsy (47%) and unilateral sixth nerve palsy (27%). No fourth nerve palsies were observed. Following EETS, 60% of patients with preoperative visual deficit had normal visual fields. For those with third and sixth nerve palsies preoperatively, 43 and 75%, respectively, had return to normal function postoperatively. SIPAP tumor characteristics were not related to postoperative cranial nerve recovery. In this series of surgically treated patients with pituitary apoplexy, all cranial nerve deficits normalized or improved following surgery. The tumor SIPAP classification was not associated with patient outcome. Though in a small series, the presented results suggest surgical treatment is beneficial for these patients.
垂体卒中(PA)是垂体肿瘤的一种罕见并发症,可表现出多种症状,包括突发的颅神经功能缺损。在患者病情稳定并进行激素替代治疗后,通常建议进行手术减压。手术减压的时机仍存在争议。在本病例系列中,我们描述了本院对接受内镜鼻内经蝶窦(EETS)手术治疗PA患者的颅神经恢复情况的经验,同时使用鞍上、鞍下、鞍旁、前后(SIPAP)分类法根据肿瘤分期评估结果。
本研究是一项单机构回顾性队列研究。
对2009年11月至2018年8月期间所有接受EETS垂体肿瘤切除术的病例进行回顾性分析。由经过培训的人员查询医院数据库,以确定采用EETS方法治疗的PA病例。从病历中提取基线特征、肿瘤类型、内分泌数据以及基于术前磁共振成像(MRI)的SIPAP分类和手术特征。提取每位患者随访期间的术后结果。
共确定15例PA患者。患者平均随访期为30个月。入院时存在的颅神经功能缺损包括视力缺损(33%);单侧动眼神经麻痹(47%)和单侧外展神经麻痹(27%)。未观察到滑车神经麻痹。EETS手术后,术前有视力缺损的患者中60%视野恢复正常。术前有动眼神经和外展神经麻痹的患者,术后分别有43%和75%恢复正常功能。SIPAP肿瘤特征与术后颅神经恢复无关。
在这组接受手术治疗的垂体卒中患者中,所有颅神经功能缺损在术后均恢复正常或有所改善。肿瘤的SIPAP分类与患者预后无关。尽管本系列病例数量较少,但所呈现的结果表明手术治疗对这些患者有益。