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Effect of primary empty sella syndrome on pituitary surgery for Cushing's disease: Clinical article

机译:原发性空蝶鞍综合征对库欣病垂体手术的影响:临床文章

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Object. Primary empty sella syndrome (ESS) results from herniation of arachnoid mater into the pituitary fossa. It has been suggested to have a negative effect on pituitary surgery; however, outcomes in this cohort have not been defined. This study was performed to determine the effect of ESS on immediate and long-term biochemical outcome after pituitary surgery for Cushing's disease (CD). Methods. Using a matched cohort study design, the authors followed patients treated with pituitary surgery for CD with and without ESS. Complete ESS was defined as pituitary gland height ≤ 2 mm, whereas partial ESS was defined as pituitary gland height > 2 mm but less than three-quarters of the total sellar depth. The primary end points were immediate and long-term biochemical outcome. Cerebrospinal fluid leaks were recorded as a secondary end point. Results. Seventy-eight patients with CD and primary ESS were identified and matched with 78 patients with CD without ESS. After surgical management, immediate biochemical remission was achieved in 69 patients (88%) with ESS and 75 controls (96%, p = 0.10). Long-term remission was achieved in most patients in both groups (5-year cure: 85% vs 92%, p = 0.10). Among patients with ESS, the presence of complete ESS predicted a worse long-term outcome (p = 0.04). Intraoperative CSF leaks were significantly more frequent with ESS (54% vs 24%, p < 0.001), and despite sellar floor repair, the rate of postoperative CSF leaks was also increased (6% vs 3%, p = 0.27). Conclusions. Biochemical outcome after pituitary surgery for CD was worse in patients with complete ESS, and the risk of a CSF leak was increased with both partial and complete ESS. However, as outcome remains superior to those following alternative therapies and the biology of these tumors is unchanged in the setting of ESS, pituitary surgery should remain the initial treatment of choice.
机译:目的。原发性空蝶鞍综合征(ESS)是蛛网膜下腔突入垂体窝的结果。有人建议对垂体手术有负面影响。但是,该队列的结果尚未确定。进行这项研究是为了确定ESS对库欣病(CD)垂体手术后即时和长期生化结果的影响。方法。使用匹配的队列研究设计,作者追踪了垂体手术治疗的伴或不伴ESS的CD患者。完整的ESS被定义为垂体高度≤2 mm,而部分ESS的定义为垂体高度> 2 mm但小于总蝶鞍深度的四分之三。主要终点是即时和长期生化结果。脑脊液漏被记录为次要终点。结果。确定了78例CD​​和原发性ESS患者,并将其与78例无ESS的CD患者匹配。手术治疗后,有69例ESS患者(88%)和75例对照(96%,p = 0.10)立即获得生化缓解。两组中的大多数患者均实现了长期缓解(5年治愈率:85%比92%,p = 0.10)。在ESS患者中,完整ESS的存在预示了较差的长期预后(p = 0.04)。 ESS术中脑脊液漏的发生率明显更高(54%vs 24%,p <0.001),尽管鞍底修复,但术后脑脊液漏的发生率也有所增加(6%vs 3%,p = 0.27)。结论。完全ESS患者垂体手术后CD的生化结果较差,部分和完全ESS患者脑脊液漏的风险增加。但是,由于结局仍然优于替代疗法,并且在ESS的情况下这些肿瘤的生物学特性没有改变,因此垂体手术应仍是首选治疗方法。

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