颅咽管瘤治疗的外科方面。

IF 1.7 Q2 SURGERY Innovative Surgical Sciences Pub Date : 2020-10-30 eCollection Date: 2021-03-01 DOI:10.1515/iss-2019-1004
Shingo Fujio, Tomoko Hanada, Masanori Yonenaga, Yushi Nagano, Mika Habu, Kazunori Arita, Koji Yoshimoto
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引用次数: 4

摘要

目的:手术切除是颅咽管瘤治疗的金标准。然而,人们担心,积极的手术切除可能导致内分泌、代谢和行为疾病的高发率。次全切除术(SR)与后续放射治疗(RT)可以减少手术并发症,但也可能增加肿瘤复发的风险和放射引起的副作用。因此,最佳手术策略仍有争议。方法:对我院收治的39例新诊断颅咽管瘤患者(男19例,女20例)的临床病程进行评估,以确定最佳手术策略。诊断时的中位年龄为34岁(范围:0-76岁)。中位随访期为8.5年(3-160个月)。我们的治疗策略包括对无手术风险的颅咽管瘤患者进行总切除(GTR)。相反,在充分的肿瘤减压后,我们对有风险的患者使用RT,主要是伽玛刀放射手术。我们根据疗程将患者分为三组:GTR, SR + RT, SR +分期手术。我们比较了三组患者的肿瘤特征以及术前和末次随访时的患者情况。结果:GTR组8例,SR + RT组21例,SR +分期手术组10例。两组患者在最大肿瘤直径、肿瘤体积、组成、钙化程度等方面均无差异。39例患者中,经颅显微手术24例,经蝶窦手术15例。无手术死亡、脑脊液漏、视觉功能严重恶化或严重下丘脑损伤病例。GTR组未见肿瘤复发。1例患者需要额外的放疗,1例患者因肿瘤复发接受了第二次手术。在分期手术的SR组中,10例患者中有8例最终接受了RT,但所有患者在最新随访时均实现了肿瘤控制。在本组中,第三次经蝶窦手术造成1例患者严重血管损伤。最后随访时,33例(85%)患者行垂体前叶激素替代术,尿崩症发生率为51%。两组间垂体功能障碍发生率差异无统计学意义。结论:我们观察到手术并发症发生率低,肿瘤控制率高。尽管尝试保存垂体柄,我们发现很难恢复垂体前叶的功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Surgical aspects in craniopharyngioma treatment.

Objectives: Total surgical resection is the gold standard in the treatment of craniopharyngioma. However, there is concern that aggressive surgical resection might result in high rates of endocrinologic, metabolic, and behavioral morbidities. Subtotal resection (SR) with subsequent radiation therapy (RT) may reduce surgical complications, but it may also increase the risk of tumor recurrence and radiation-induced side effects. Therefore, the optimal surgical strategy remains debatable.

Methods: To determine the optimal surgical strategy, we assessed the clinical courses of 39 patients (19 male patients and 20 female patients) with newly diagnosed craniopharyngioma who were treated at our institute. The median age at diagnosis was 34 years (range: 0-76 years). The median follow-up period was 8.5 years (range: 3-160 months). Our treatment strategy comprised gross total resection (GTR) for craniopharyngioma in patients that were not at surgical risk. Conversely, after adequate tumor decompression, we used RT, mainly Gamma Knife radiosurgery, in patients at risk. We divided the patients into the following three groups depending on the treatment course: GTR, SR with RT, and SR with staged surgery. We compared tumor characteristics, as well as patients' conditions at the preoperative stage and last follow-up, among the three groups.

Results: There were 8, 21, and 10 patients in the GTR, SR with RT, and SR with staged surgery groups, respectively. There were no differences in the maximum tumor diameter, tumor volume, composition, and presence of calcification among the groups. Among the 39 patients, 24 underwent transcranial microsurgery and 15 underwent trans-sphenoidal surgery as the initial treatment. No cases involving surgical mortality, cerebrospinal fluid leakage, severely deteriorated visual function, or severe hypothalamic damage were observed. No tumor recurrence was noted in the GTR group. One patient required additional RT, and one patient underwent second surgery for tumor recurrence in the SR with RT group. In the SR with staged surgery group, 8 of the 10 patients eventually underwent RT, but tumor control was achieved in all patients at the latest follow-up. In this group, the third trans-sphenoidal surgery caused a severe vascular injury in one patient. At the final follow-up, 33 (85%) patients were undergoing anterior pituitary hormone replacement, and the rate of diabetes insipidus was 51%. There was no significant difference in the pituitary dysfunction rate among the groups.

Conclusions: We observed a low rate of surgical complications and a sufficient tumor control rate in response to our treatment strategy. Despite attempting preservation of the pituitary stalk, we found it difficult to rescue anterior pituitary function.

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