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16例促甲状腺激素垂体腺瘤患者的长期手术结果

Long-term surgical outcome in 16 patients with thyrotropin pituitary adenoma.

作者信息

Sanno N, Teramoto A, Osamura R Y

机构信息

Department of Neurosurgery, Nippon Medical School, Tama-city, Tokyo, Japan.

出版信息

J Neurosurg. 2000 Aug;93(2):194-200. doi: 10.3171/jns.2000.93.2.0194.

Abstract

OBJECT

Thyrotropin-secreting pituitary adenomas are rare lesions of the endocrinological system. Although introduction of a hypersensitive radioimmunoassay for thyrotropin enables the recognition of inappropriate secretion of this hormone, the aforementioned lesions remain uncommon and unfamiliar to most neurosurgeons. It has been reported previously that surgical cure of thyrotropin-secreting adenomas is more difficult than in other functional adenomas because of the large size and invasive features of the former. However, the long-term outcome after surgery has not been well documented. The authors report on a surgical series of 16 patients with thyrotropin adenoma and the results of long-term follow up.

METHODS

Sixteen patients ages 23 to 62 years (12 women and four men) underwent transsphenoidal removal of thyrotropin adenomas between 1983 and 1999. These patients had the syndrome of inappropriate thyrotropin secretion (SITS) with pituitary mass lesions. Four of the patients had undergone previous subtotal thyroidectomy and/or radioiodine thyroid ablation, and 11 had been treated with antithyroid medication. Radiological investigations demonstrated macroadenomas in 14 patients, and 10 of those had cavernous sinus invasion. Surgical findings showed unusually fibrous and firm tumors in 13 (81.2%) of 16 patients. Preoperative octreotide administration was revealed to be effective for serum thyrotropin reduction as well as tumor shrinkage. Transsphenoidal surgery was performed with no morbidity resulting. Surgical remission was achieved in 10 (62.5%) of 16 patients, and total remission was achieved in 14 patients (87.5%) with a combination of additional radiation or medical therapy. In the other two patients, SITS persisted because of tumor rests in the cavernous sinus. Therefore, radiation and/or antithyroid therapy was administered. In the mean follow-up period of 7.5 years (range 11 months-15.8 years), no recurrence of tumor was observed on magnetic resonance images, whereas recurrence of SITS was found in two patients with no tumor regrowth. In addition, coexistent primary hyperthyroidism was found in two other patients despite remission of SITS after surgery.

CONCLUSIONS

Transsphenoidal surgery can achieve a good long-term outcome in patients with thyrotropin-secreting pituitary adenomas if surgery is performed before these become larger, invasive tumors. In the authors' experience, thyrotropin-secreting adenomas are fibrous and firm, which makes it difficult to achieve surgical remission. In addition, even satisfactory resection of the tumor sometimes results in recurrence of SITS or hyperthyroid symptoms due to coexistent primary hyperthyroidism. It is emphasized that a careful follow-up review is necessary after surgery, especially in patients with a long preoperative history of hyperthyroidism.

摘要

目的

促甲状腺素分泌型垂体腺瘤是内分泌系统的罕见病变。尽管超敏促甲状腺素放射免疫测定法的引入使得能够识别该激素的不适当分泌,但上述病变对大多数神经外科医生来说仍然不常见且不熟悉。先前有报道称,由于促甲状腺素分泌型腺瘤体积大且具有侵袭性,其手术治愈比其他功能性腺瘤更困难。然而,手术后的长期结果尚未得到充分记录。作者报告了一组16例促甲状腺素腺瘤患者的手术情况及长期随访结果。

方法

1983年至1999年间,16例年龄在23至62岁之间的患者(12名女性和4名男性)接受了经蝶窦切除促甲状腺素腺瘤手术。这些患者患有伴有垂体肿块病变的促甲状腺素不适当分泌综合征(SITS)。其中4例患者先前接受过甲状腺次全切除术和/或放射性碘甲状腺消融术,11例患者接受过抗甲状腺药物治疗。影像学检查显示14例患者为大腺瘤,其中10例侵犯海绵窦。手术发现16例患者中有13例(81.2%)的肿瘤异常纤维化且质地坚硬。术前使用奥曲肽被证明对降低血清促甲状腺素以及缩小肿瘤有效。经蝶窦手术未导致任何并发症。16例患者中有10例(62.5%)实现了手术缓解,14例患者(87.5%)通过联合额外的放疗或药物治疗实现了完全缓解。另外2例患者由于海绵窦内残留肿瘤组织,SITS持续存在。因此,给予了放疗和/或抗甲状腺治疗。在平均7.5年的随访期(范围为11个月至15.8年)内,磁共振成像未观察到肿瘤复发,而在2例无肿瘤复发的患者中发现了SITS复发。此外,另外2例患者尽管手术后SITS缓解,但仍存在原发性甲状腺功能亢进。

结论

如果在促甲状腺素分泌型垂体腺瘤发展为更大的侵袭性肿瘤之前进行手术,经蝶窦手术可以在这类患者中取得良好的长期效果。根据作者的经验,促甲状腺素分泌型腺瘤纤维化且质地坚硬,这使得实现手术缓解较为困难。此外,即使肿瘤切除令人满意,有时也会由于并存的原发性甲状腺功能亢进导致SITS复发或甲状腺功能亢进症状复发。强调手术后需要进行仔细的随访复查,尤其是对于术前有长期甲状腺功能亢进病史的患者。

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