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垂体炎叠加于无功能垂体腺瘤:诊断性临床、内分泌及放射学特征

Hypophysitis superimposed on a non-functioning pituitary adenoma: diagnostic clinical, endocrine, and radiologic features.

作者信息

Ballian N, Chrisoulidou A, Nomikos P, Samara C, Kontogeorgos G, Kaltsas G A

机构信息

Department of Surgery, The University of Wisconsin Hospital and Clinics, 600 Highland Avenue, Madison, WI 53792, USA.

出版信息

J Endocrinol Invest. 2007 Sep;30(8):677-83. doi: 10.1007/BF03347449.

Abstract

Pituitary adenomas are common neoplasms requiring medical and/or surgical treatment when associated with hormonal hypersecretion. Treatment of non-functioning pituitary adenomas is necessary when symptoms of mass effect or hormonal deficits occur. However, therapeutic options, including surgical resection and/or radiotherapy, can be associated with significant complications. Hence, it is important to consider disorders that could present in a similar manner to pituitary adenomas, for which surgery is not the indicated therapeutic approach. We describe herein a 38-yr-old woman who presented with a pituitary lesion that was considered to be a non-functioning pituitary adenoma. Due to lack of hormonal deficits and/or compression of adjacent structures, we opted for conservative management and followup with consecutive magnetic resonance imaging. Fifteen months after initial diagnosis, considerable enlargement of the lesion was noted, extending mainly superiorly and indenting the optic chiasm. Repeated endocrine investigation revealed partial anterior pituitary insufficiency. The patient underwent trans-sphenoidal resection of the pituitary lesion; histology revealed a null cell pituitary adenoma and lymphocytic hypophysitis (LYH) of the non-neoplastic adenohypophysial gland. Post-operatively, complete anterior and partial posterior pituitary insufficiency developed. This case illustrates the effects of new-onset LYH in a patient with a pre-existing non-functioning pituitary adenoma. Being aware of this rare possibility is important, as enlargement of the pituitary lesion may not be caused by expansion of the preexisting tumor, but by the onset of LYH of the nonneoplastic pituitary tissue.

摘要

垂体腺瘤是常见的肿瘤,当伴有激素分泌过多时需要药物和/或手术治疗。当出现占位效应或激素缺乏症状时,无功能性垂体腺瘤也需要治疗。然而,包括手术切除和/或放疗在内的治疗选择可能会伴有严重并发症。因此,考虑那些可能以与垂体腺瘤相似的方式出现但手术并非首选治疗方法的疾病很重要。我们在此描述一名38岁女性,她有一个被认为是无功能性垂体腺瘤的垂体病变。由于缺乏激素缺乏和/或邻近结构受压,我们选择了保守治疗并通过连续磁共振成像进行随访。初始诊断15个月后,发现病变显著增大,主要向上扩展并压迫视交叉。重复的内分泌检查显示部分垂体前叶功能减退。患者接受了经蝶窦垂体病变切除术;组织学检查显示为无功能垂体腺瘤和非肿瘤性腺垂体的淋巴细胞性垂体炎(LYH)。术后出现了完全性垂体前叶功能减退和部分垂体后叶功能减退。该病例说明了新发LYH对一名已有无功能性垂体腺瘤患者的影响。认识到这种罕见的可能性很重要,因为垂体病变的增大可能不是由原有肿瘤的扩展引起的,而是由非肿瘤性垂体组织发生LYH所致。

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