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卡麦角林治疗伴有自发性脑脊液鼻漏的巨大侵袭性泌乳素瘤后诱发的气颅。

Cabergoline-Induced Pneumocephalus Following Treatment for Giant Invasive Macroprolactinoma Presenting With Spontaneous Cerebrospinal Fluid Rhinorrhea.

作者信息

Elabd Souha S, Ahmad Maswood M, Qetab Sameer Q, Almalki Mussa Hussain

机构信息

Obesity, Endocrine, and Metabolism Center, King Fahad Medical City, Riyadh, Saudi Arabia.

King Hussein Medical City,Internal Medicine Department, Amman, Jordan.

出版信息

Clin Med Insights Endocrinol Diabetes. 2018 Feb 13;11:1179551418758640. doi: 10.1177/1179551418758640. eCollection 2018.

Abstract

Cerebrospinal fluid (CSF) rhinorrhea is rarely reported as the first presenting feature of giant invasive macroprolactinomas. Cerebrospinal fluid rhinorrhea is usually reported as a complication of trauma, neurosurgical, and skull-based procedures (such as pituitary surgery or radiations), and less frequently after medical treatment with dopamine agonists (DAs) for macroprolactinomas. This phenomenon results from fistula creation that communicates between the subarachnoid space and the nasal cavity. Meanwhile, pneumocephalus is another well-recognized complication after transsphenoidal surgery for pituitary macroadenomas. This entity may present with nausea, vomiting, headache, dizziness, and more seriously with seizures and/or a decreased level of consciousness if tension pneumocephalus develops. Case reports about the occurrence of spontaneous pneumocephalus after medical treatment with DAs without prior surgical interventions are scarce in the literature. Our index case is a young man who was recently diagnosed with a giant invasive prolactin-secreting pituitary macroadenoma with skull base destruction. A few months before this diagnosis, he presented with spontaneous CSF rhinorrhea with no history of previous medical or surgical treatment. In this case report, we report an uncommon presentation for giant invasive macroprolactinoma with a CSF leak treated with cabergoline that was subsequently complicated by meningitis and pneumocephalus. This is a very rare complication of cabergoline therapy, which occurred approximately 1 month after treatment initiation.

摘要

脑脊液鼻漏很少被报道为巨大侵袭性泌乳素瘤的首发症状。脑脊液鼻漏通常被报道为创伤、神经外科手术和颅底手术(如垂体手术或放疗)的并发症,而在使用多巴胺激动剂(DAs)药物治疗泌乳素瘤后较少见。这种现象是由于蛛网膜下腔与鼻腔之间形成瘘管所致。同时,气颅是垂体大腺瘤经蝶窦手术后另一种公认的并发症。如果发生张力性气颅,该病症可能表现为恶心、呕吐、头痛、头晕,更严重的是癫痫发作和/或意识水平下降。文献中关于在未进行手术干预的情况下使用DAs药物治疗后发生自发性气颅的病例报告很少。我们的索引病例是一名年轻男性,最近被诊断为患有巨大侵袭性分泌泌乳素的垂体大腺瘤并伴有颅底破坏。在确诊前几个月,他出现了自发性脑脊液鼻漏,既往无药物或手术治疗史。在本病例报告中,我们报告了一例罕见的巨大侵袭性泌乳素瘤伴脑脊液漏的病例,该患者接受卡麦角林治疗,随后并发脑膜炎和气颅。这是卡麦角林治疗非常罕见的并发症,发生在治疗开始后约1个月。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbe3/5815410/74cc89ffb356/10.1177_1179551418758640-fig1.jpg

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