Açikgöz Bektaş, Cağavi Ferda, Hakki Tekkök Ismail
Department of Neurosurgery, Zonguldak Karaelmas University, Zonguldak, Turkey.
J Clin Neurosci. 2004 Jun;11(5):555-9. doi: 10.1016/j.jocn.2003.07.006.
Pituitary apoplexy is an uncommon syndrome characterised by sudden onset of headache, meningeal signs, visual disturbances, ophthalmoplegia and confusion. Documented recurrent apoplexy or treated apoplexy is even rarer with only few reports in the literature. Between 1994 and 2001, 18 patients were treated for pituitary apoplexy at Bayindir Medical Centre through transsphenoidal route. In all, topical bromocriptine was applied after tumour resection as described by Ozgen. We hereby present the cases of two patients with recurrent apoplexy 3 and 7 years after the initial surgical treatment for pituitary adenoma with apoplexy. The patients were treated non-surgically with success. Additional treatment in the form of radiosurgery was found necessary for the first patient. Surgical excision of the pituitary tumours with apoplexy reduces the risk of recurrent bleedings but eradication is not a rule. These patients need to be followed closely in the postoperative period for possible recurrence of bleeding.
垂体卒中是一种罕见的综合征,其特征为突然出现头痛、脑膜刺激征、视力障碍、眼肌麻痹和意识模糊。有记录的复发性卒中或经治疗的卒中更为罕见,文献中仅有少数报道。1994年至2001年间,巴因迪尔医疗中心通过经蝶窦途径对18例垂体卒中患者进行了治疗。总体而言,按照奥兹根的描述,在肿瘤切除后应用了局部溴隐亭。在此,我们报告两例垂体腺瘤卒中初次手术治疗后3年和7年出现复发性卒中的病例。这两名患者接受了非手术治疗并取得成功。发现第一名患者有必要接受放射外科等额外治疗。对伴有卒中的垂体肿瘤进行手术切除可降低复发性出血的风险,但并非总能根除肿瘤。这些患者术后需要密切随访,以防出血复发。