Yusra Jamal, Yudi Camacho, Simon Hanft, Patrick Chiarolanzio, Michael D Goldberg, Jamie A Mullally
{"title":"A Case of Pituitary Apoplexy and Cavernous Sinus Syndrome during Hemodialysis.","authors":"Yusra Jamal, Yudi Camacho, Simon Hanft, Patrick Chiarolanzio, Michael D Goldberg, Jamie A Mullally","doi":"10.1155/2023/3183088","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Pituitary apoplexy (PA) is a clinical syndrome of pituitary hemorrhage or infarction and can result in hypopituitarism as well as compression of adjacent brain structures. Visual loss occurs frequently, as a result of tumor expansion and compression of the optic chiasm and optic nerves. Additionally, with pituitary tumor invasion into the fixed space of the cavernous sinus, compression of multiple cranial nerves can result in cavernous sinus syndrome (CSS). We describe a case of an undiagnosed pituitary tumor manifesting as abrupt PA with CSS during hemodialysis (HD). <i>Clinical Case</i>. A 77-year-old male with end-stage renal disease (ESRD) presented with acute onset of severe headache, decreased vision, ophthalmoplegia of the left eye, and hypotension during HD. MRI of the brain revealed a 2.5 cm pituitary adenoma with acute hemorrhage, compression of the left prechiasmatic optic nerve, and invasion into the left cavernous sinus (CS). The hormonal profile was consistent with multiple pituitary hormone deficiencies. The patient was treated with glucocorticoids and underwent transsphenoidal resection of the tumor. He had an uneventful postoperative hospital course, and his left visual acuity stabilized, although there was no immediate improvement in his other ocular symptoms.</p><p><strong>Conclusion: </strong>Our case highlights a rare constellation of a pituitary adenoma with CS invasion complicated by PA and CSS during HD. The pathophysiology of PA is not well understood, and there are very limited data regarding PA in patients with end-stage renal disease (ESRD) on HD. Prompt recognition of PA in a patient presenting with CSS, particularly in the HD setting, is essential to ensure appropriate care is provided for this medical emergency.</p>","PeriodicalId":9621,"journal":{"name":"Case Reports in Endocrinology","volume":null,"pages":null},"PeriodicalIF":0.9000,"publicationDate":"2023-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154637/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Endocrinology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2023/3183088","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Pituitary apoplexy (PA) is a clinical syndrome of pituitary hemorrhage or infarction and can result in hypopituitarism as well as compression of adjacent brain structures. Visual loss occurs frequently, as a result of tumor expansion and compression of the optic chiasm and optic nerves. Additionally, with pituitary tumor invasion into the fixed space of the cavernous sinus, compression of multiple cranial nerves can result in cavernous sinus syndrome (CSS). We describe a case of an undiagnosed pituitary tumor manifesting as abrupt PA with CSS during hemodialysis (HD). Clinical Case. A 77-year-old male with end-stage renal disease (ESRD) presented with acute onset of severe headache, decreased vision, ophthalmoplegia of the left eye, and hypotension during HD. MRI of the brain revealed a 2.5 cm pituitary adenoma with acute hemorrhage, compression of the left prechiasmatic optic nerve, and invasion into the left cavernous sinus (CS). The hormonal profile was consistent with multiple pituitary hormone deficiencies. The patient was treated with glucocorticoids and underwent transsphenoidal resection of the tumor. He had an uneventful postoperative hospital course, and his left visual acuity stabilized, although there was no immediate improvement in his other ocular symptoms.
Conclusion: Our case highlights a rare constellation of a pituitary adenoma with CS invasion complicated by PA and CSS during HD. The pathophysiology of PA is not well understood, and there are very limited data regarding PA in patients with end-stage renal disease (ESRD) on HD. Prompt recognition of PA in a patient presenting with CSS, particularly in the HD setting, is essential to ensure appropriate care is provided for this medical emergency.
背景:垂体性脑瘫(PA)是垂体出血或梗死的一种临床综合征,可导致垂体功能减退以及邻近脑部结构受压。由于肿瘤扩张并压迫视丘和视神经,视力丧失的情况经常发生。此外,垂体瘤侵入海绵窦的固定空间,压迫多条颅神经可导致海绵窦综合征(CSS)。我们描述了一例未确诊的垂体瘤患者在血液透析(HD)过程中突然出现 PA 并伴有 CSS 的病例。临床病例。一名患有终末期肾病(ESRD)的 77 岁男性患者在接受血液透析(HD)治疗期间突发剧烈头痛、视力下降、左眼眼球震颤和低血压。脑部核磁共振成像显示,垂体腺瘤2.5厘米,急性出血,压迫左侧视前神经,并侵犯左侧海绵窦(CS)。激素谱符合多种垂体激素缺乏症的特征。患者接受了糖皮质激素治疗,并接受了经蝶窦肿瘤切除术。术后住院过程顺利,左眼视力稳定,但其他眼部症状没有立即改善:我们的病例突显了一种罕见的情况,即垂体腺瘤有 CS 侵犯,在 HD 期间并发 PA 和 CSS。目前对 PA 的病理生理学尚不十分清楚,有关终末期肾病(ESRD)患者在接受 HD 治疗期间出现 PA 的数据也非常有限。在出现 CSS 的患者中及时识别 PA 至关重要,尤其是在 HD 环境中,以确保为这种医疗紧急情况提供适当的护理。