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并存的原发性空蝶鞍综合征和肢端肥大症。

Coexisting primary empty sella syndrome and acromegally.

作者信息

Molitch M E, Hieshima G B, Marcovitz S, Jackson I M, Wolpert S

出版信息

Clin Endocrinol (Oxf). 1977 Sep;7(3):261-3. doi: 10.1111/j.1365-2265.1977.tb01323.x.

Abstract

The 'empty' sells syndrome is now a more frequent diagnosis due to the increased use of pneumoencephalography in the evaluation of the enlarged pituitary fossa. This syndrome has also been classified into a 'primary' form in which there has been no prior pituitary irradiation or surgery, and a 'secondary' form in which the empty sella is found after such procedures. Most patients with the primary empty sella syndrome are found to have normal pituitary function while about 30% have varying degrees of hypopituitarism (Neelon et al., 1973). It is not widely appreciated, however, that the primary empty sella may harbour a pituitary tumour with resultant acromegaly. In this report we describe two such patients who presented with active acromegaly. This entity of pituitary tumour in a primary empty sella merits careful consideration since the coexistence of these two findings may influence the therapeutic approach that might otherwise be appropriate for the pituitary tumour.

摘要

由于在评估扩大的垂体窝时气脑造影术的使用增加,“空泡蝶鞍”综合征现在是一种更常见的诊断。该综合征也被分为“原发性”形式,即既往无垂体放疗或手术史,以及“继发性”形式,即在这些手术后发现空蝶鞍。大多数原发性空蝶鞍综合征患者的垂体功能正常,而约30%有不同程度的垂体功能减退(尼隆等人,1973年)。然而,原发性空蝶鞍可能隐匿垂体肿瘤并导致肢端肥大症,这一点尚未得到广泛认识。在本报告中,我们描述了两名表现为活动性肢端肥大症的此类患者。原发性空蝶鞍中存在垂体肿瘤这一情况值得仔细考虑,因为这两种发现并存可能会影响原本适用于垂体肿瘤的治疗方法。

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