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十二例垂体转移瘤:病例系列及文献复习。

Twelve cases of pituitary metastasis: a case series and review of the literature.

机构信息

Department of Medicine, Nursing and Health Sciences, Monash University, Melbourne, Australia.

Department of Neurosurgery, Monash Medical Centre, Melbourne, Australia.

出版信息

Pituitary. 2018 Oct;21(5):463-473. doi: 10.1007/s11102-018-0899-x.

Abstract

PURPOSE

The pituitary gland is an unusual site for metastatic spread, but as patients with metastatic malignancy are living longer, it may become more prevalent. Compression of important anatomy adjacent to the sella may produce disabling symptoms and endocrine derangement, leading to significant morbidity.

METHODS

An ambispective review of patient records between 2013 and 2017 from three neurosurgical centres was performed. After identifying cases, further investigation was performed to evaluate patient demographic, symptoms at presentation, radiological and histological findings, management, and outcome.

RESULTS

Our investigation identified 12 patients with pituitary metastasis. The average age of the cases was 63.4 years, with breast (n = 4) and lung (n = 4) being the most common primary cancers. In half the cases there was a history of metastatic disease, while in one-quarter of cases, pituitary symptoms were the first sign of malignancy. Adenohypophyseal dysfunction (83%), diabetes insipidus (DI) (75%), headache (67%) and visual field defects (67%) were the most common findings at presentation. Glucocorticoid replacement increased the sensitivity for diagnosis of DI. All cases were contrast enhancing on MRI and the endoscopic trans-sphenoidal approach was preferred for biopsy and debulking.

CONCLUSIONS

The pituitary should not be overlooked as a site of metastasis and sellar symptoms may be the first presentation of neoplastic disease. Any biochemical or clinical sign of pituitary pathology in a patient with known cancer should raise suspicion for sellar metastasis. Moreover, the development of DI or ophthalmoplegia from any pituitary lesion is suggestive of metastatic disease even in patients with no known primary.

摘要

目的

垂体是转移的罕见部位,但随着转移性恶性肿瘤患者的存活时间延长,其发病率可能会增加。鞍旁重要解剖结构受压可导致严重的致残性症状和内分泌紊乱,导致发病率显著增加。

方法

对 2013 年至 2017 年间来自 3 个神经外科中心的 12 例垂体转移患者的病历进行回顾性分析。在确定病例后,进一步进行调查以评估患者的人口统计学特征、发病时的症状、影像学和组织学发现、治疗方法和结果。

结果

我们的调查共发现 12 例垂体转移患者。病例的平均年龄为 63.4 岁,最常见的原发癌为乳腺癌(n=4)和肺癌(n=4)。半数患者有转移性疾病病史,1/4 的病例中,垂体症状是恶性肿瘤的首发表现。腺垂体功能减退(83%)、尿崩症(75%)、头痛(67%)和视野缺损(67%)是发病时最常见的表现。糖皮质激素替代治疗提高了诊断尿崩症的敏感性。所有病例的 MRI 均增强,经蝶窦内镜入路优先用于活检和减瘤。

结论

垂体不应被忽视为转移部位,鞍区症状可能是肿瘤性疾病的首发表现。在已知患有癌症的患者中,任何垂体病变的生化或临床迹象都应怀疑存在鞍区转移。此外,即使在无已知原发性疾病的患者中,任何垂体病变引起的尿崩症或眼肌麻痹都提示转移性疾病。

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