临床误诊误治
臨床誤診誤治
림상오진오치
CLINICAL MISDIAGNOSIS & MISTHERAPY
2015年
2期
53-55
,共3页
嗜铬细胞瘤%抽搐%误诊%癫痫
嗜鉻細胞瘤%抽搐%誤診%癲癇
기락세포류%추휵%오진%전간
Pheochromocytoma%Tics%Misdiagnosis%Epilepsy
目的:探讨以抽搐为首发表现的多发性嗜铬细胞瘤的误诊原因及防范措施。方法回顾性分析2006年我院收治的1例以抽搐为首发表现的多发性嗜铬细胞瘤误诊为癫痫的临床资料。结果患儿因间断性抽搐伴意识丧失19个月入院,曾在外院就诊,诊断为癫痫、高血压脑病及多发性大动脉炎,给予相应治疗效果不佳,遂就诊我院。腹部超声检查提示肾上腺区多发性结节,行超声引导下穿刺活检术,活组织病理检查诊断为嗜铬细胞瘤,予手术切除病灶。术后病理检查证实诊断。随访7年,抽搐未再发作,肿瘤无复发。结论临床上对伴血压异常的抽搐患者,要考虑到嗜铬细胞瘤可能,应及时行相关检查以确诊。
目的:探討以抽搐為首髮錶現的多髮性嗜鉻細胞瘤的誤診原因及防範措施。方法迴顧性分析2006年我院收治的1例以抽搐為首髮錶現的多髮性嗜鉻細胞瘤誤診為癲癇的臨床資料。結果患兒因間斷性抽搐伴意識喪失19箇月入院,曾在外院就診,診斷為癲癇、高血壓腦病及多髮性大動脈炎,給予相應治療效果不佳,遂就診我院。腹部超聲檢查提示腎上腺區多髮性結節,行超聲引導下穿刺活檢術,活組織病理檢查診斷為嗜鉻細胞瘤,予手術切除病竈。術後病理檢查證實診斷。隨訪7年,抽搐未再髮作,腫瘤無複髮。結論臨床上對伴血壓異常的抽搐患者,要攷慮到嗜鉻細胞瘤可能,應及時行相關檢查以確診。
목적:탐토이추휵위수발표현적다발성기락세포류적오진원인급방범조시。방법회고성분석2006년아원수치적1례이추휵위수발표현적다발성기락세포류오진위전간적림상자료。결과환인인간단성추휵반의식상실19개월입원,증재외원취진,진단위전간、고혈압뇌병급다발성대동맥염,급여상응치료효과불가,수취진아원。복부초성검사제시신상선구다발성결절,행초성인도하천자활검술,활조직병리검사진단위기락세포류,여수술절제병조。술후병리검사증실진단。수방7년,추휵미재발작,종류무복발。결론림상상대반혈압이상적추휵환자,요고필도기락세포류가능,응급시행상관검사이학진。
Objective To summarize the misdiagnosis cause and preventive measures of multiple pheochromocytoma presented as convulsion. Methods A retrospective analysis was conducted on a multiple pheochromocytoma with convulsion misdiagnosed as epilepsy in 2006. Results The patient suffered from intermittent attacks with convulsions and loss of con-sciousness for 19 months. He has misdiagnosed as having epilepsy, hypertensive encephalopathy and Takayasu′s arteritis in other hospitals. The condition was not relieved after symptomatic treatment, and the patient was admitted to our hospital for another attack. Abdominal ultrasound confirmed adrenal gland multiple nodules, and then it was diagnosed as pheochromocy-toma by the puncture biopsy guided by ultrasound. All the lesions were totally removed, and were diagnosed as multiple pheo-chromocytoma confirmed by pathological examination. The patient did not have a relapse of convulsions, and there was no tumor recurrence during a 7-year follow up. Conclusion The patients with convulsion and abnormal blood pressure should be suspected as having pheochromocytoma and corresponding tests should be made.