Su Deng-Huang, Chang Ying-Chun, Chang Tien-Chun, Chang Ching-Chung, Tsai Ken-Sung, Huang Tien-Shang
Department of Internal Medicine, College of Medicine, National Taiwan University and National Taiwan University Hospital, Taipei, Taiwan.
J Formos Med Assoc. 2003 May;102(5):292-8.
Diagnosis and management of Cushing's syndrome is a challenge to the endocrinologist. This retrospective study investigated the etiology, clinical presentation, treatment and prognosis of endogenous Cushing's syndrome and compared the differences of prognostic factors between Cushing's disease patients with macroadenoma and microadenoma.
Data on disease history, physical examination, and biochemistry of Cushing's syndrome and factors related to the prognosis of Cushing's disease were analyzed.
A total of 61 consecutive patients (52 women and 9 men) with endogenous Cushing's syndrome treated from January 1992 to July 2002 were included in this study. They comprised 31 cases of adrenal adenoma, 19 cases of Cushing's disease, 6 cases of ectopic adrenocorticotropin (ACTH) syndrome, 3 cases of adrenal carcinoma, 1 case of macronodular hyperplasia, and 1 case of micronodular hyperplasia. ACTH-independent Cushing's syndrome was the most frequent etiology in this series. The most common symptoms and signs were moon face (89%), weight gain (74%), buffalo hump (74%), and truncal obesity (72%). Hypercholesterolemia was noted in 27 of 45 patients (60.0%) checked for total serum cholesterol level. Elevation of serum lactate dehydrogenase was found in 29 (74.3%) of 39 patients assessed. Patients with adrenal adenoma had the highest cure rate. High residual (2/17, 11.8%) and recurrent rates (5/17, 29.4%) were found in patients with Cushing's disease. There were no significant differences in prognostic factors between Cushing's disease patients with macroadenoma and microadenoma.
ACTH-independent Cushing's syndrome was the most frequent type of Cushing's syndrome in this series. The dyslipidemia and elevation of lactate dehydrogenase activity in this series indicated the need for routine laboratory testing in Cushing's syndrome patients. This study found no significant differences in prognostic factors between Cushing's disease patients with macroadenoma and microadenoma.
库欣综合征的诊断与管理对内分泌科医生而言是一项挑战。本回顾性研究调查了内源性库欣综合征的病因、临床表现、治疗及预后,并比较了大腺瘤和微腺瘤库欣病患者预后因素的差异。
分析了库欣综合征的病史、体格检查、生化指标及与库欣病预后相关的因素。
本研究纳入了1992年1月至2002年7月间连续治疗的61例内源性库欣综合征患者(52例女性,9例男性)。其中包括肾上腺腺瘤31例、库欣病19例、异位促肾上腺皮质激素(ACTH)综合征6例、肾上腺皮质癌3例、大结节性增生1例和小结节性增生1例。本系列中促肾上腺皮质激素非依赖性库欣综合征是最常见的病因。最常见的症状和体征为满月脸(89%)、体重增加(74%)、水牛背(74%)和向心性肥胖(72%)。45例检测总血清胆固醇水平的患者中有27例(60.0%)存在高胆固醇血症。39例接受评估的患者中有29例(74.3%)血清乳酸脱氢酶升高。肾上腺腺瘤患者的治愈率最高。库欣病患者的残留率(2/17,11.8%)和复发率(5/17,29.4%)较高。大腺瘤和微腺瘤库欣病患者的预后因素无显著差异。
促肾上腺皮质激素非依赖性库欣综合征是本系列中最常见的库欣综合征类型。本系列中的血脂异常和乳酸脱氢酶活性升高表明库欣综合征患者需要进行常规实验室检查。本研究发现大腺瘤和微腺瘤库欣病患者的预后因素无显著差异。