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以少见表现为首发症状的9例嗜铬细胞瘤临床分析
引用本文:何丽,余学锋.以少见表现为首发症状的9例嗜铬细胞瘤临床分析[J].内科急危重症杂志,2013(6):350-352.
作者姓名:何丽  余学锋
作者单位:[1]新疆克拉玛依市中心医院 [2]华中科技大学同济医学院附属同济医院,武汉430030
摘    要:目的:探讨以少见表现为首发症状的的嗜铬细胞瘤的临床特点.方法:回顾性分析经手术病理证实为嗜铬细胞瘤并具有特殊临床表现的9例患者的临床资料结果:2例患者术前诊断为急性冠脉综合征;2例患者术前诊断休克;1例患者术前诊断为糖尿病酮症酸中毒;4例患者术前诊断为视神经炎.所有患者均有高血压.影像学检查均发现肾上腺占位病变,均经手术病理证实为肾上腺嗜铬细胞瘤,术后症状好转.结论:嗜铬细胞瘤表现多样化,高血压是重要的诊断线索,实验室及影像学检查对明确诊断有重要意义.

关 键 词:嗜铬细胞瘤  急性冠脉综合征  糖尿病酮症酸中毒  休克  视神经炎

Nine cases of pheochromocytoma with rare initial clinical manifestations
HE Li,YU Xue-feng.Nine cases of pheochromocytoma with rare initial clinical manifestations[J].Journal of Internal Intensive Medicine,2013(6):350-352.
Authors:HE Li  YU Xue-feng
Institution:. Tongji Hospital Affiliated to Tongii Medical College, Huazhong University of Science and Technology, Wuhan 430030 , China
Abstract:Objective : To discuss the clinical characteristics of 9 cases of pheochromocytoma with rare clinical manifestation as the initial symptoms. Methods: The clinical data of 9 cases of pheochromocytoma confirmed by operation and pathological finding were analyzed retrospectively. Results: Two cases were diagnosed as acute coronary syndrome, 2 as shock, 1 as diabetic ketoacidosis and 4 as optic neuritis before operation. All patients suffered from hypertension. Imaging studies revealed adrenal mass. All cases were confirmed as adrenal pheochromocytoma by operation and pathological examination. Clinical symptoms of 9 cases were improved after operation. Conclusion : The clinical manifestations of pheochromocytoma are multiplicity, hypertension is an important diagnostic clue, laboratory and imaging exmninations are crucial for the diagnosis of pheochromocytoma.
Keywords:Pheochromocytoma Acute coronary syndrome Diabetic ketoacidosis Shock Optic neuritis
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