{"title":"一位蝶鞍空洞症病人呈現反覆眩暈、耳鳴表現及合併術後鼻漏的照護經驗分享","authors":"張彥清 張彥清, 劉淑芬 Yen-Ching Chang, 許庭綾 Shu-Fen Liu, 湯其暾 Ting-Ling Hsu, 朱大同 Chi-Tun Tang","doi":"10.53106/2410325x2021120802010","DOIUrl":null,"url":null,"abstract":"\n 本案例為一名56歲女性因反覆眩暈及耳鳴,經檢查後初步診斷為良性陣發性姿勢性眩暈(Benign Paroxysmal Positional Vertigo, BPPV),接受右耳耳石復位術(Canalith Reposition Procedure),然而,隨著病程進展,接續出現關鍵性的前額眉心處的頭痛及視力模糊的症狀,藉由詳細地病史詢問、身體評估、及相關的檢驗及影像檢查,採用排除及納入相關診斷的鑑別過程,最後確診為蝶鞍空洞症,在詳細地病情解釋後,病人接受經鼻腔內視鏡蝶竇蝶鞍減壓併自體脂肪填充及鼻中隔皮瓣重建手術。不幸地,術後產生腦脊髓液鼻漏的併發症,在及時地重新評估、鑑別診斷及處置,有效的控制併發症避免神經功能惡化,最後病人順利出院,因此引發筆者撰寫動機,期望分享此病例照護經驗,提醒同仁臨床照護病人時需要時刻保持警覺,確保病人回復健康。\n The case in this study is a 56-year-old woman who was initially diagnosed with benign paroxysmal postural dizziness because of repeated vertigo and tinnitus after serial examinations. She underwent reduction of otolith of right ear (Canalith Reposition Procedure). However, her symptoms remained and subsequent symptoms of frontal headache and blurred vision occurred. Although symptoms such as vertigo, tinnitus, and headache are common in Meniere’s disease, benign paroxysmal postural vertigo (BPPV), cerebral infarction, etc. eventually we revised the diagnosis to the Empty Sella Syndrome through detailed inquiry of medical history, physical assessment, and image examinations.After well-addressed explanation of the clinical condition, the patient received endoscopic transnasal transsphenoidal approach and packing sella with autologous fat, reconstruction by cartilage and nasal septal flap. Unfortunately, the sequel of cerebrospinal fluid rhinorrhea occurred after the operation. By promptly reassessment, differential diagnosis with proper treatment, the complication was effectively controlled to avoid neurological deterioration, and the patient was discharged without further complication. I sincerely share the experience of this specific case with my colleagues. Keeping vigilant in clinical care of patients to ensure they could return to health.\n \n","PeriodicalId":177436,"journal":{"name":"台灣專科護理師學刊","volume":"3 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"台灣專科護理師學刊","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.53106/2410325x2021120802010","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
本案例為一名56歲女性因反覆眩暈及耳鳴,經檢查後初步診斷為良性陣發性姿勢性眩暈(Benign Paroxysmal Positional Vertigo, BPPV),接受右耳耳石復位術(Canalith Reposition Procedure),然而,隨著病程進展,接續出現關鍵性的前額眉心處的頭痛及視力模糊的症狀,藉由詳細地病史詢問、身體評估、及相關的檢驗及影像檢查,採用排除及納入相關診斷的鑑別過程,最後確診為蝶鞍空洞症,在詳細地病情解釋後,病人接受經鼻腔內視鏡蝶竇蝶鞍減壓併自體脂肪填充及鼻中隔皮瓣重建手術。不幸地,術後產生腦脊髓液鼻漏的併發症,在及時地重新評估、鑑別診斷及處置,有效的控制併發症避免神經功能惡化,最後病人順利出院,因此引發筆者撰寫動機,期望分享此病例照護經驗,提醒同仁臨床照護病人時需要時刻保持警覺,確保病人回復健康。
The case in this study is a 56-year-old woman who was initially diagnosed with benign paroxysmal postural dizziness because of repeated vertigo and tinnitus after serial examinations. She underwent reduction of otolith of right ear (Canalith Reposition Procedure). However, her symptoms remained and subsequent symptoms of frontal headache and blurred vision occurred. Although symptoms such as vertigo, tinnitus, and headache are common in Meniere’s disease, benign paroxysmal postural vertigo (BPPV), cerebral infarction, etc. eventually we revised the diagnosis to the Empty Sella Syndrome through detailed inquiry of medical history, physical assessment, and image examinations.After well-addressed explanation of the clinical condition, the patient received endoscopic transnasal transsphenoidal approach and packing sella with autologous fat, reconstruction by cartilage and nasal septal flap. Unfortunately, the sequel of cerebrospinal fluid rhinorrhea occurred after the operation. By promptly reassessment, differential diagnosis with proper treatment, the complication was effectively controlled to avoid neurological deterioration, and the patient was discharged without further complication. I sincerely share the experience of this specific case with my colleagues. Keeping vigilant in clinical care of patients to ensure they could return to health.
本案例为一名56岁女性因反复眩晕及耳鸣,经检查后初步诊断为良性阵发性姿势性眩晕(Benign Paroxysmal Positional Vertigo, BPPV),接受右耳耳石复位术(Canalith Reposition Procedure),然而,随著病程进展,接续出现关键性的前额眉心处的头痛及视力模糊的症状,借由详细地病史询问、身体评估、及相关的检验及影像检查,采用排除及纳入相关诊断的鉴别过程,最后确诊为蝶鞍空洞症,在详细地病情解释后,病人接受经鼻腔内视镜蝶窦蝶鞍减压并自体脂肪填充及鼻中隔皮瓣重建手术。不幸地,术后产生脑脊髓液鼻漏的并发症,在及时地重新评估、鉴别诊断及处置,有效的控制并发症避免神经功能恶化,最后病人顺利出院,因此引发笔者撰写动机,期望分享此病例照护经验,提醒同仁临床照护病人时需要时刻保持警觉,确保病人回复健康。 The case in this study is a 56-year-old woman who was initially diagnosed with benign paroxysmal postural dizziness because of repeated vertigo and tinnitus after serial examinations. She underwent reduction of otolith of right ear (Canalith Reposition Procedure). However, her symptoms remained and subsequent symptoms of frontal headache and blurred vision occurred. Although symptoms such as vertigo, tinnitus, and headache are common in Meniere’s disease, benign paroxysmal postural vertigo (BPPV), cerebral infarction, etc. eventually we revised the diagnosis to the Empty Sella Syndrome through detailed inquiry of medical history, physical assessment, and image examinations.After well-addressed explanation of the clinical condition, the patient received endoscopic transnasal transsphenoidal approach and packing sella with autologous fat, reconstruction by cartilage and nasal septal flap. Unfortunately, the sequel of cerebrospinal fluid rhinorrhea occurred after the operation. By promptly reassessment, differential diagnosis with proper treatment, the complication was effectively controlled to avoid neurological deterioration, and the patient was discharged without further complication. I sincerely share the experience of this specific case with my colleagues. Keeping vigilant in clinical care of patients to ensure they could return to health.