An unusual presentation of hypopituitarism caused by a sellar aneurysm.

IF 1.6 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM Archives of Endocrinology Metabolism Pub Date : 2024-04-26 eCollection Date: 2024-01-01 DOI:10.20945/2359-4292-2023-0224
Tijana Ičin, Kristina Stepanović, Ivana Bajkin, Nikola Boban, Dragan Anđelić, Đorđe Popović, Jovana Prodanović Simeunović, Željka Savić
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Abstract

Hypopituitarism is a rare clinical condition that can present as a partial or complete absence of pituitary hormones. Hypopituitarism is most commonly caused by a sellar or parasellar mass, particularly a tumor, and the gold standard for its differential diagnosis is magnetic resonance imaging (MRI). Intrasellar aneurysm is an unusual cause of hypopituitarism. Indeed, about 0.17% of all cases of hypopituitarism are due to intrasellar aneurysms. We report the case of a 72-year-old man who was admitted to the hospital due to gastrointestinal symptoms and malnourishment. Due to persistent hyponatremia and spontaneous hypoglycemia in laboratory findings, the examination of the hypothalamic-pituitary-adrenal axis was eventually initiated, and the patient was later diagnosed with an unruptured aneurysm of the ophthalmic segment of the right internal carotid artery with sellar extension as a cause of panhypopituitarism. A combined endovascular treatment was performed with stent-assisted coil embolization of the aneurysm, and the patient was prescribed oral hormonal therapy. At the 1-year follow-up visit, no improvement in pituitary function was observed, and a pituitary MRI showed complete aneurysm occlusion and partial empty sella with significantly decreased pituitary volume. Aneurysms of the internal carotid artery are rare and may be associated with hypopituitarism and delayed diagnosis due to their unusual clinical presentation. Endovascular procedures, such as coil embolization of the aneurysm, could be the treatment of choice in these patients. Persistent hypopituitarism may occur even after successful treatment of the aneurysm.

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蝶窦动脉瘤导致垂体功能减退症的不寻常表现。
垂体功能减退症是一种罕见的临床症状,可表现为垂体激素部分或完全缺失。垂体功能减退症最常见的病因是蝶鞍或蝶鞍旁肿块,尤其是肿瘤,其鉴别诊断的金标准是磁共振成像(MRI)。鞘内动脉瘤是导致垂体功能减退症的不常见原因。事实上,在所有垂体功能减退症病例中,约有 0.17% 是由小脑内动脉瘤引起的。我们报告了一例 72 岁的男性病例,他因胃肠道症状和营养不良而入院。由于实验室检查结果显示持续性低钠血症和自发性低血糖,最终开始对下丘脑-垂体-肾上腺轴进行检查,患者随后被诊断为右侧颈内动脉眼段未破裂动脉瘤,并伴有蝶鞍扩展,这是导致泛垂体功能障碍的原因之一。患者接受了支架辅助线圈栓塞动脉瘤的联合血管内治疗,并接受了口服激素治疗。一年随访时,垂体功能未见改善,垂体核磁共振成像显示动脉瘤完全闭塞,部分蝶鞍空洞,垂体体积明显缩小。颈内动脉瘤非常罕见,由于临床表现不寻常,可能与垂体功能减退和诊断延迟有关。血管内手术,如动脉瘤线圈栓塞术,可能是治疗这些患者的首选方法。即使成功治疗了动脉瘤,也可能出现持续性垂体功能减退。
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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来源期刊
Archives of Endocrinology Metabolism
Archives of Endocrinology Metabolism Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.90
自引率
5.90%
发文量
107
审稿时长
7 weeks
期刊介绍: The Archives of Endocrinology and Metabolism - AE&M – is the official journal of the Brazilian Society of Endocrinology and Metabolism - SBEM, which is affiliated with the Brazilian Medical Association. Edited since 1951, the AE&M aims at publishing articles on scientific themes in the basic translational and clinical area of Endocrinology and Metabolism. The printed version AE&M is published in 6 issues/year. The full electronic issue is open access in the SciELO - Scientific Electronic Library Online e at the AE&M site: www.aem-sbem.com. From volume 59 on, the name was changed to Archives of Endocrinology and Metabolism, and it became mandatory for manuscripts to be submitted in English for the online issue. However, for the printed issue it is still optional for the articles to be sent in English or Portuguese. The journal is published six times a year, with one issue every two months.
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